神经可塑性:修订间差异

维基百科,自由的百科全书
删除的内容 添加的内容
It's gonna be awesome留言 | 贡献
无编辑摘要
It's gonna be awesome留言 | 贡献
无编辑摘要
第1行: 第1行:
{{medical}}
{{medical}}
{{expand|time=2011-05-23T02:55:33+00:00}}
'''神经可塑性'''(英語:'''Neuro-plasticity''')是指的由于经验原因引起的[[大脑]]的结构改变。神经可塑性是近期的发现,过去的科学家往往认为在婴儿[[关键期]]后,大脑结构往往不发生变化。
'''神经可塑性'''(英語:'''Neuro-plasticity''')是指的由于经验原因引起的[[大脑]]的结构改变。神经可塑性是近期的发现,过去的科学家往往认为在婴儿[[关键期]]后,大脑结构往往不发生变化。
大脑有神经元细胞和[[神经胶质细胞]]构成,这些细胞互相连接,通过加强或削弱这些连接,大脑的结构可以发生改变。
大脑有神经元细胞和[[神经胶质细胞]]构成,这些细胞互相连接,通过加强或削弱这些连接,大脑的结构可以发生改变。
{{trans H}}
'''Neuroplasticity''', also known as '''brain plasticity''' or '''neural plasticity''', is an [[umbrella term]] that describes lasting change to the brain throughout an individual's life course. The term gained prominence in the latter half of the 20th century, when new research<ref name='livingston'/><ref name="science.sciencemag.org">{{cite journal | author = Bennett EL, Diamond MC, Krech D, Rosenzweig MR | year = 1964 | title = Chemical and Anatomical Plasticity of the Brain | url = http://science.sciencemag.org/content/146/3644/160 | journal = Science | volume = 146 | issue = | pages = 610–619 | doi=10.1126/science.146.3644.610 | pmid=14191699}}</ref> showed that many aspects of the brain can be altered (or are "plastic") even into adulthood.<ref name="Rakic 2002"/> This notion is in contrast with the previous scientific consensus that the brain develops during a [[critical period]] in early childhood and then remains relatively unchanged (or "static").<ref name="Pascual-Leone et al. 2005"/>

Neuroplasticity can be observed at multiple scales, from microscopic changes in individual [[neurons]] to larger-scale changes such as [[cortical remapping]] in response to injury. However, cortical remapping is more extensive early in development.<ref name="Pascual-Leone et al. 2011"/> Behavior, [[Environmental enrichment (neural)|environmental stimuli]], thought, and emotions may also cause neuroplastic change through [[activity-dependent plasticity]], which has significant implications for healthy development, learning, memory, and recovery from [[brain damage]].<ref name="Pascual-Leone et al. 2011"/><ref name="Activity-dependent neural plasticity">
{{cite journal
| vauthors = Ganguly K, Poo MM
| title = Activity-dependent neural plasticity from bench to bedside
| journal = Neuron
| volume = 80
| issue = 3
| pages = 729–741
| date = October 2013
| pmid = 24183023
| doi = 10.1016/j.neuron.2013.10.028}}</ref><ref>
{{cite journal
| vauthors = Keller TA, Just MA
| title = Structural and functional neuroplasticity in human learning of spatial routes
| journal = NeuroImage
| volume = 125
| issue =
| pages = 256–266
| date = January 2016
| pmid = 26477660
| doi = 10.1016/j.neuroimage.2015.10.015
| quote = Recent findings with both animals and humans suggest that decreases in microscopic movements of water in the hippocampus reflect short-term neuroplasticity resulting from learning. Here we examine whether such neuroplastic structural changes concurrently alter the functional connectivity between hippocampus and other regions involved in learning.&nbsp;... These concurrent changes characterize the multidimensionality of neuroplasticity as it enables human spatial learning.}}</ref>

At the single cell level, [[synaptic plasticity]] refers to changes in the connections between neurons, whereas [[non-synaptic plasticity]] refers to changes in their intrinsic excitability.
{{TOC limit|3}}

== Localizationism ==
From the late 1500s neurologists largely supported the theory of [[Functional specialization (brain)|localizationism]], which holds that the brain comprises functionally specialized areas. The famed astronomer [[Galileo Galilei]] is credited{{by whom|date=March 2017}} with the origins of localizationism. According to [[Norman Doidge]], Galileo's studies of space and its celestial bodies led him to believe that "all nature functioned as a large cosmic clock" and that these bodies "began to explain individual living things, including our bodily organs, mechanistically".<ref name=":0">{{Cite book|title= The Brain that Changes Itself|last= Doidge|first= Norman|publisher= Penguin Books|year= 2007|isbn= |location= |pages= 22}}</ref> He saw the universe as a giant machine rather than as a living organism. When applied to the brain, this means that its parts have hardwired functions as a machine has parts designated to a certain area.<ref name=":0"/> According to this theory, the functional specialization of each brain area could mean that localized damage to one area would lead to a loss of the function that it served. This led physicians to consider certain diseases or conditions arising from brain damage as untreatable.

== Neurobiology ==
One of the fundamental principles underlying neuroplasticity is based on the idea that individual [[synapse|synaptic connections]] are constantly being [[synaptic pruning|removed]] or [[Synaptogenesis|recreated]], largely dependent upon the activity of the neurons that bear them. The activity-dependence of [[synaptic plasticity]] is captured in the [[aphorism]] which is often used to summarize [[Hebbian theory]]: "neurons that fire together, wire together"/"neurons that fire out of sync, fail to link". If two nearby neurons often produce an [[action potential|impulse]] in close temporal proximity, their functional properties may converge. Conversely, neurons that are not regularly activated simultaneously may be less likely to functionally converge.

=== Cortical maps ===
Cortical organization, especially in [[sensory system]]s, is often described in terms of [[cortical map|maps]].<ref name="Buonomano et al 1998" /> For example, sensory information from the foot projects to one cortical site and the projections from the hand target another site. As a result, the cortical representation of sensory inputs from the body resembles a [[Somatotopic arrangement|somatotopic map]], often described as the [[Cortical homunculus|sensory homunculus]].

In the late 1970s and early 1980s, several groups began exploring the impact of interfering with [[wikt:sensation|sensory inputs]] on cortical map reorganization. [[Michael Merzenich]], [[Jon Kaas]] and Doug Rasmusson were some of those researchers. They found that if the cortical map is deprived of its input, it activates at a later time in response to other, usually adjacent inputs. Their findings have been since corroborated and extended by many research groups. Merzenich's (1984) study involved the mapping of [[owl monkey]] hands before and after [[amputation]] of the third digit. Before amputation, there were five distinct areas, one corresponding to each digit of the experimental hand. Sixty-two days following amputation of the third [[Digit (anatomy)|digit]], the area in the [[cortical map]] formerly occupied by that digit had been invaded by the previously adjacent second and fourth digit zones. The areas representing digit one and five are not located directly beside the area representing digit three, so these regions remained, for the most part, unchanged following amputation.<ref name="Merzenich et al 1984" /> This study demonstrates that only those regions that border a certain area invade it to alter the cortical map. In the somatic sensory system, in which this phenomenon has been most thoroughly investigated, JT Wall and J Xu have traced the mechanisms underlying this plasticity. Re-organization is not cortically [[emergence|emergent]], but occurs at every level in the processing hierarchy; this produces the map changes observed in the cerebral cortex.<ref name="Wall et al 2002" />

Merzenich and William Jenkins (1990) initiated studies relating [[sensory experience]], without pathological perturbation, to cortically observed plasticity in the [[primate]] [[somatosensory system]], with the finding that sensory sites activated in an attended [[operant behavior]] increase in their cortical representation. Shortly thereafter, Ford Ebner and colleagues (1994) made similar efforts in the [[rodent]] [[whisker]] [[barrel cortex]] (also part of the somatosensory system). These two groups largely diverged over the years. The rodent whisker barrel efforts became a focus for Ebner, Matthew Diamond, Michael Armstrong-James, Robert Sachdev, and Kevin Fox. Great inroads were made in identifying the locus of change as being at cortical [[synapse]]s [[gene expression|expressing]] [[NMDA receptor]]s, and in implicating [[cholinergic]] inputs as necessary for normal expression. The work of Ron Frostig and Daniel Polley (1999, 2004) identified [[behavioral]] manipulations causing a substantial impact on the cortical plasticity in that system.

[[Michael Merzenich|Merzenich]] and DT Blake (2002, 2005, 2006) went on to use cortical implants to study the evolution of plasticity in both the [[somatosensory]] and [[auditory system]]s. Both systems show similar changes with respect to [[behavior]]. When a stimulus is cognitively associated with [[reinforcement]], its cortical representation is strengthened and enlarged. In some cases, cortical representations can increase two to threefold in 1–2 days when a new sensory motor behavior is first acquired, and changes are largely finalised within at most a few weeks. Control studies show that these changes are not caused by sensory experience alone: they require learning about the sensory experience, they are strongest for the stimuli that are associated with reward, and they occur with equal ease in operant and classical conditioning behaviors.

An interesting phenomenon involving plasticity of cortical maps is the phenomenon of [[phantom limb]] sensation. Phantom limb sensation is experienced by people who have undergone [[amputation]]s in hands, arms, and legs, but it is not limited to extremities. Although the neurological basis of phantom limb sensation is still not entirely understood it is believed that cortical reorganization plays an important role.<ref name="Doidge 2007" />

[[Norman Doidge]], following the lead of Michael Merzenich, separates manifestations of neuroplasticity into adaptations that have positive or negative behavioral consequences. For example, if an organism can recover after a stroke to normal levels of performance, that adaptiveness could be considered an example of "positive plasticity". Changes such as an excessive level of neuronal growth leading to [[spasticity]] or [[tonic paralysis]], or excessive [[neurotransmitter]] release in response to injury that could result in nerve cell death, are considered as an example of "negative" plasticity. In addition, drug addiction and obsessive-compulsive disorder are both deemed examples of "negative plasticity" by Dr. Doidge, as the synaptic rewiring resulting in these behaviors is also highly maladaptive.<ref name="Doidge 2007"/><ref>[http://www.childrenofthecode.org/interviews/merzenich.htm Interview with Merzenich], 2004</ref>

A 2005 study found that the effects of neuroplasticity occur even more rapidly than previously expected. Medical students' brains were imaged during the period of studying for their exams. In a matter of months, the students' gray matter increased significantly in the posterior and lateral parietal cortex.<ref>Draganski et al. "[http://www.jneurosci.org/cgi/content/abstract/26/23/6314 Temporal and Spatial Dynamics of Brain Structure Changes during Extensive Learning]" The Journal of Neuroscience, 7 June 2006, 26(23):6314–6317</ref>

== Applications and example ==

The adult brain is not entirely "hard-wired" with fixed [[neuronal circuit]]s. There are many instances of cortical and subcortical rewiring of neuronal circuits in response to training as well as in response to injury. There is solid evidence that [[neurogenesis]] (birth of brain cells) occurs in the adult, mammalian brain—and such changes can persist well into old age.<ref name="Rakic 2002"/> The evidence for neurogenesis is mainly restricted to the [[hippocampus]] and [[olfactory bulb]], but current research has revealed that other parts of the brain, including the cerebellum, may be involved as well.<ref name="Ponti et al 2008"/>

There is now ample evidence {{citation needed|reason=What evidence?|date=January 2016}} for the active, experience-dependent re-organization of the synaptic networks of the brain involving multiple inter-related structures including the cerebral cortex. The specific details of how this process occurs at the molecular and [[ultrastructure|ultrastructural]] levels are topics of active neuroscience research. The way experience can influence the synaptic organization of the brain is also the basis for a number of theories of brain function including the general theory of mind and [[Neural Darwinism]]. The concept of neuroplasticity is also central to theories of memory and learning that are associated with experience-driven alteration of synaptic structure and function in studies of [[classical conditioning]] in invertebrate animal models such as ''[[Aplysia]]''.

=== Treatment of brain damage ===

A surprising consequence of neuroplasticity is that the brain activity associated with a given function can be transferred to a different location; this can result from normal experience and also occurs in the process of recovery from brain injury. Neuroplasticity is the fundamental issue that supports the scientific basis for treatment of [[acquired brain injury]] with goal-directed experiential therapeutic programs in the context of [[Rehabilitation (neuropsychology)|rehabilitation]] approaches to the functional consequences of the injury.

Neuroplasticity is gaining popularity as a theory that, at least in part, explains improvements in functional outcomes with physical therapy post-stroke. Rehabilitation techniques that are supported by evidence which suggest cortical reorganization as the mechanism of change include [[constraint-induced movement therapy]], [[functional electrical stimulation]], treadmill training with body-weight support, and [[virtual reality therapy]]. [[Robot#Healthcare|Robot assisted therapy]] is an emerging technique, which is also hypothesized to work by way of neuroplasticity, though there is currently insufficient evidence to determine the exact mechanisms of change when using this method.<ref>{{cite journal | author = Young J. A., Tolentino M. | year = 2011 | title = Neuroplasticity and its Applications for Rehabilitation | url = | journal = American Journal of Therapeutics | volume = 18 | issue = 1| pages = 70–80 | pmid = 21192249 | last2 = Tolentino | doi = 10.1097/MJT.0b013e3181e0f1a4 }}</ref>

One group has developed a treatment that includes increased levels of [[progesterone]] injections in brain-injured patients. "Administration of progesterone after traumatic brain injury<ref>[http://wayback.archive.org/web/20060626124922/http://www.whsc.emory.edu/press_releases_video.cfm?id=brain_trauma Traumatic Brain Injury] (a story of TBI and the results of ProTECT using progesterone treatments) Emory University News Archives</ref> (TBI) and stroke reduces [[edema]], inflammation, and neuronal cell death, and enhances spatial reference memory and sensory motor recovery."<ref name="Cutler et al 2005">{{cite journal |last1=Cutler |first1=Sarah M. |last2=Hoffman |first2=Stuart W. |last3=Pettus |first3=Edward H. |last4=Stein |first4=Donald G. |date=October 2005 |title=Tapered progesterone withdrawal enhances behavioral and molecular recovery after traumatic brain injury |journal=Experimental Neurology |volume=195 |issue=2 |page= |pages=423–429 |publisher=Elsevier |doi=10.1016/j.expneurol.2005.06.003 |url= |language= |pmid=16039652}}</ref> In a clinical trial, a group of severely injured patients had a 60% reduction in mortality after three days of progesterone injections.<ref name="stein_interview">Stein, Donald. "Plasticity." Personal interview. Alyssa Walz. 19 November 2008.</ref> However, a study published in the ''[[The New England Journal of Medicine|New England Journal of Medicine]]'' in 2014 detailing the results of a multi-center NIH-funded phase III clinical trial of 882 patients found that treatment of acute traumatic brain injury with the hormone progesterone provides no significant benefit to patients when compared with placebo.<ref>[http://news.emory.edu/stories/2014/12/protectiii_results_progesterone_tbi/ Progesterone offers no significant benefit in traumatic brain injury clinical trial], Emory University, Atlanta, GA</ref>

=== Vision ===
For decades, researchers assumed that humans had to acquire [[binocular vision]], in particular [[stereopsis]], in early childhood or they would never gain it. In recent years, however, successful improvements in persons with [[amblyopia]], [[convergence insufficiency]] or other stereo vision anomalies have become prime examples of neuroplasticity; binocular vision improvements and [[stereopsis recovery]] are now active areas of scientific and clinical research.<ref>Dominick M. Maino: [http://www.revoptom.com/continuing_education/tabviewtest/lessonid/106025/dnnprintmode/true/skinsrc/ Neuroplasticity: Teaching an Old Brain New Tricks], Review of Optometry, January 2009</ref><ref name="vedamurthy-etal-2012">{{cite news|author1=Indu Vedamurthy|author2=Samuel J. Huang|author3=Dennis M. Levi|author4=Daphne Bavelier|author5=David C. Knill|title=Recovery of stereopsis in adults through training in a virtual reality task|journal=Journal of Vision|date=27 December 2012|volume=12|number=14|doi=10.1167/12.14.53}} Article 53</ref><ref>{{cite news|author1=Robert F. Hess|author2=Benjamin Thompson|title=New insights into amblyopia: binocular therapy and noninvasive brain stimulation|journal=Journal of AAPOS|date=February 2013|volume=17|number=1|pages=89–93|doi=10.1016/j.jaapos.2012.10.018}}</ref>

=== Brain training===
Several companies have offered so-called [[cognitive training]] software programs for various purposes that claim to work via neuroplasticity; one example is [[Fast ForWord]] which is marketed to help children with [[learning disabilities]].<ref name=Fastmeta/> A systematic meta-analytic review found that "There is no evidence from the analysis carried out that Fast ForWord is effective as a treatment for children's oral language or reading difficulties".<ref name=Fastmeta>{{cite journal
|vauthors=Strong GK, Torgerson CJ, Torgerson D, Hulme C
| date = Mar 2011
| title = A systematic meta-analytic review of evidence for the effectiveness of the 'Fast ForWord' language intervention program
| url =
| journal = J Child Psychol Psychiatry
| volume = 52
| issue = 3
| pages = 224–35
| doi = 10.1111/j.1469-7610.2010.02329.x
| pmid=20950285
| pmc=3061204}}</ref>
A 2016 review found very little evidence supporting any of the claims of Fast ForWord and other commercial products, as their task-specific effects fail to generalise to other tasks.<ref>{{cite journal
|vauthors = Simons DJ, Boot WR, Charness N, Gathercole SE, Chabris CF, Hambrick DZ, Stine-Morrow EA
| publication-date =
| year = 2016
| title = Do "Brain-Training" Programs Work?
| journal = Psychological Science in the Public Interest
| volume = 17
| issue = 3
| pages = 103–186
| doi = 10.1177/1529100616661983
| url = http://m.psi.sagepub.com/content/17/3/103.full.pdf
| pmid=27697851}}</ref>

===Sensory prostheses===
Neuroplasticity is involved in the development of sensory function. The brain is born immature and it adapts to sensory inputs after birth. In the auditory system, congenital hearing impairment, a rather frequent inborn condition affecting 1 of 1000 newborns, has been shown to affect auditory development, and implantation of a [[cochlear implant|sensory prostheses]] activating the auditory system has prevented the deficits and induced functional maturation of the auditory system.<ref>{{cite journal | author = Kral A, Sharma A | year = 2012 | title = Developmental Neuroplasticity after Cochlear Implantation | url = | journal = Trends Neurosci | volume = 35 | issue = 2| pages = 111–122 | pmid = 22104561 | last2 = Sharma | doi = 10.1016/j.tins.2011.09.004 | pmc = 3561718 }}</ref> Due to a sensitive period for plasticity, there is also a sensitive period for such intervention within the first 2–4 years of life. Consequently, in prelingually deaf children, early [[cochlear implant]]ation, as a rule, allows to learn the mother language and acquire acoustic communication.<ref>{{cite journal |vauthors=Kral A, O'Donoghue GM | year = 2010 | title = Profound Deafness in Childhood | url = | journal = New England J Medicine | volume = 363 | issue = | pages = 1438–50 | doi=10.1056/nejmra0911225 | pmid=20925546}}</ref>

===Phantom limbs===
[[File:Mirror-box-comic.jpg|thumb|right|200px|A diagrammatic explanation of the mirror box. The patient places the intact limb into one side of the box (in this case the right hand) and the amputated limb into the other side. Due to the mirror, the patient sees a reflection of the intact hand where the missing limb would be (indicated in lower contrast). The patient thus receives artificial visual feedback that the "resurrected" limb is now moving when they move the good hand.]]
{{Main|Phantom limb|Mirror box}}
In the phenomenon of [[phantom limb]] sensation, a person continues to feel pain or sensation within a part of their body that has been [[Amputation|amputated]]. This is strangely common, occurring in 60–80% of amputees.<ref>{{cite journal|last=Beaumont|first=Geneviève |author2=Mercier, Pierre-Emmanuel |author3=Malouin, Jackson|title=Decreasing phantom limb pain through observation of action and imagery: A case series|journal=Pain Medicine|year=2011|volume=12|issue=2|pages=289–299|doi=10.1111/j.1526-4637.2010.01048.x|pmid=21276185}}</ref> An [[Phantom limb#Neurological basis|explanation]] for this is based on the concept of neuroplasticity, as the cortical maps of the removed limbs are believed to have become engaged with the area around them in the [[postcentral gyrus]]. This results in activity within the surrounding area of the cortex being misinterpreted by the area of the cortex formerly responsible for the amputated limb.

The relationship between phantom limb sensation and neuroplasticity is a complex one. In the early 1990s V.S. Ramachandran theorized that phantom limbs were the result of cortical remapping. However, in 1995 Herta Flor and her colleagues demonstrated that cortical remapping occurs only in patients who have phantom pain.<ref>{{cite journal | author = Flor H, Elbert T, Knecht S, Wienbruch C, Pantev C, Birbaumer N | year = 1995 | title = Phantom-limb pain as a perceptual correlate of cortical reorganization following arm amputation | url = | journal = Nature | volume = 375 | issue = 6531| pages = 482–484 | pmid = 7777055 | last2 = Elbert | last3 = Knecht | last4 = Wienbruch | last5 = Pantev | last6 = Birbaumer | last7 = Larbig | last8 = Taub | doi = 10.1038/375482a0 |display-authors=etal}}</ref> Her research showed that phantom limb pain (rather than referred sensations) was the perceptual correlate of cortical reorganization.<ref>Flor H, Cortical Reorganization And Chronic Pain: Implications For Rehabilitation, J Rehabil Med, 2003, Suppl.41:66–72</ref> This phenomenon is sometimes referred to as maladaptive plasticity.

In 2009 Lorimer Moseley and Peter Brugger carried out a remarkable experiment in which they encouraged arm amputee subjects to use visual imagery to contort their phantom limbs into impossible configurations. Four of the seven subjects succeeded in performing impossible movements of the phantom limb. This experiment suggests that the subjects had modified the neural representation of their phantom limbs and generated the motor commands needed to execute impossible movements in the absence of feedback from the body.<ref>Moseley, Brugger, Interdependence of movement and anatomy persists when amputees learn a physiologically impossible movement of their phantom limb, PNAS, 16 September 2009,[http://www.pnas.org/content/early/2009/10/23/0907151106]</ref> The authors stated that: "In fact, this finding extends our understanding of the brain's plasticity because it is evidence that profound changes in the mental representation of the body can be induced purely by internal brain mechanisms—the brain truly does change itself."

===Chronic pain===
{{Main|Chronic pain}}
Individuals who suffer from chronic pain experience prolonged pain at sites that may have been previously injured, yet are otherwise currently healthy. This phenomenon is related to neuroplasticity due to a maladaptive reorganization of the nervous system, both peripherally and centrally. During the period of tissue damage, [[Noxious stimulus|noxious stimuli]] and [[inflammation]] cause an elevation of nociceptive input from the periphery to the central nervous system. Prolonged [[nociception]] from the periphery then elicits a neuroplastic response at the cortical level to change its [[Somatotopic arrangement|somatotopic organization]] for the painful site, inducing [[central sensitization]].<ref>{{cite journal |author1=Seifert F. |author2=Maihöfner C. | year = 2011 | title = Functional and structural imaging of pain-induced neuroplasticity | url = | journal = Current Opinion in Anaesthesiology | volume = 24 | issue = | pages = 515–523 | doi=10.1097/aco.0b013e32834a1079}}</ref> For instance, individuals experiencing [[complex regional pain syndrome]] demonstrate a diminished cortical somatotopic representation of the hand contralaterally as well as a decreased spacing between the hand and the mouth.<ref>{{cite journal |author1=Maihöfner C. |author2=Handwerker H.O. |author3=Neundorfer B. |author4=Birklein F. | year = 2003 | title = Patterns of cortical reorganization in complex regional pain syndrome | url = | journal = Neurology | volume = 61 | issue = | pages = 1707–1715 | doi=10.1212/01.wnl.0000098939.02752.8e}}</ref> Additionally, chronic pain has been reported to significantly reduce the volume of [[grey matter]] in the brain globally, and more specifically at the [[prefrontal cortex]] and right [[thalamus]].<ref>{{cite journal | author = Apkarian A.V., Sosa Y., Sonty S | year = 2004 | title = Chronic back pain is associated with decreased prefrontal and thalamic gray matter density | url = | journal = J Neurosci | volume = 24 | issue = 46| pages = 10410–10415 | pmid = 15548656 | last2 = Sosa | last3 = Sonty | last4 = Levy | last5 = Harden | last6 = Parrish | last7 = Gitelman | doi = 10.1523/JNEUROSCI.2541-04.2004 |display-authors=etal}}</ref> However, following treatment, these abnormalities in cortical reorganization and grey matter volume are resolved, as well as their symptoms. Similar results have been reported for phantom limb pain,<ref>{{cite journal | author = Karl A., Birbaumer N., Lutzenberger W. | year = 2001 | title = Reorganization of motor and somatosensory cortex in upper extremity amputees with phantom limb pain | url = | journal = J Neurosci | volume = 21 | issue = 10| pages = 3609–18 | pmid = 11331390 | last2 = Birbaumer | last3 = Lutzenberger | last4 = Cohen | last5 = Flor |display-authors=etal}}</ref> [[Low back pain#Chronic pain|chronic low back pain]]<ref>{{cite journal |author1=Flor H. |author2=Braun C. |author3=Elbert T. | year = 1997 | title = Extensive reorganization of primary somatosensory cortex in chronic back pain patients | url = | journal = Neurosci Lett | volume = 224 | issue = | pages = 5–8 | doi=10.1016/s0304-3940(97)13441-3|display-authors=etal}}</ref> and [[carpal tunnel syndrome]].<ref>{{cite journal | author = Napadow V., Kettner N., Ryan A. | year = 2006 | title = Somatosensory cortical plasticity in carpal tunnel syndrome: a cross-sectional fMRI evaluation | url = | journal = NeuroImage | volume = 31 | issue = 2| pages = 520–530 | pmid = 16460960 | last2 = Kettner | last3 = Ryan | last4 = Kwong | last5 = Audette | last6 = Hui | doi = 10.1016/j.neuroimage.2005.12.017 |display-authors=etal}}</ref>

===Meditation===
{{Main|Research on meditation}}
A number of studies have linked meditation practice to differences in cortical thickness or density of [[gray matter]].<ref>
{{Cite journal |last1=Pagnoni |first1= Giuseppe |last2=Cekic |first2=Milos | date = 28 July 2007
| title = Age effects on gray matter volume and attentional performance in Zen meditation.| journal = Neurobiology of Aging| volume = 28 | pages = 1623–1627 | issue = 10
| doi=10.1016/j.neurobiolaging.2007.06.008 | pmid=17655980}}
</ref><ref>
{{Cite journal |last1=Vestergaard-Poulsen |first1= Peter
| date = 28 January 2009
| title = Long-term meditation is associated with increased gray matter density in the brain stem.| journal = NeuroReport| volume = 20 | pages = 170–174 | issue = 2
| doi=10.1097/WNR.0b013e328320012a
|last2=van Beek |first2=Martijn
|last3=Skewes |first3=Joshua
|last4=Bjarkam |first4=Carsten R
|last5=Stubberup |first5=Michael
|last6=Bertelsen |first6=Jes
|last7=Roepstorff |first7=Andreas | pmid=19104459
}}
</ref><ref>
{{Cite journal |last1=Luders |first1=Eileen
| date = 14 January 2009
| title = The underlying anatomical correlates of long-term meditation: larger hippocampal and frontal volumes of gray matter.
| journal = NeuroImage| volume = 45 | pages = 672–678 | issue = 3 | doi=10.1016/j.neuroimage.2008.12.061
|last2=Toga |first2=Arthur W.
|last3=Lepore |first3=Natasha
|last4=Gaser |first4=Christian
}}
</ref> One of the most well-known studies to demonstrate this was led by [[Sara Lazar]], from Harvard University, in 2000.<ref>{{Cite journal |last1=Lazar |first1= S. |last2=Kerr |first2=C. |last3=Wasserman |first3=R. |last4=Gray |first4 = J.| last5 = Greve| first5 = D. | date = 28 November 2005| title = Meditation experience is associated with increased cortical thickness| journal = NeuroReport| volume = 16 | pages = 1893–97 | issue = 17 | pmc=1361002 | pmid=16272874 | doi=10.1097/01.wnr.0000186598.66243.19 |last6=Treadway |first6=Michael T. |last7=McGarvey |first7=Metta |last8=Quinn |first8=Brian T. |last9=Dusek |first9=Jeffery A.|last10= Benson |first10= Herbert |last11= Rauch |first11= Scott L. |last12= Moore |first12= Christopher I. |last13= Fischl |first13= Bruce |display-authors= 8 }}</ref> [[Richard Davidson]], a neuroscientist at the [[University of Wisconsin]], has led experiments in cooperation with the [[Dalai Lama]] on effects of meditation on the brain. His results suggest that long-term or short-term practice of meditation results in different levels of activity in brain regions associated with such qualities as [[attention]], [[anxiety]], [[Depression (mood)|depression]], [[fear]], [[anger]], the ability of the body to heal itself. These functional changes may be caused by changes in the physical structure of the brain.<ref>{{Cite journal |last1=Lutz |first1= A. |last2=Greischar |first2=L.L. |last3=Rawlings |first3=N.B. |last4=Ricard |first4 = M.| last5 = Davidson| first5 = R. J.| date = 16 November 2004| title = Long-term meditators self-induce high-amplitude gamma synchrony during mental practice| journal = PNAS| volume = 101| pages = 16369–73 |url=http://www.pnas.org/cgi/content/full/101/46/16369 |accessdate=8 July 2007 |doi=10.1073/pnas.0407401101| issue = 46 |pmid=15534199 |pmc=526201 |postscript=<!--None-->}}</ref><ref>{{cite news|date=20 January 2007 |author=Sharon Begley |publisher=http://www.dalailama.com |url=http://www.dalailama.com/news.112.htm |title=How Thinking Can Change the Brain}}</ref><ref>{{Cite journal|last1=Davidson |first1=Richard |last2=Lutz |first2=Antoine |title=Buddha's Brain: Neuroplasticity and Meditation |journal=IEEE Signal Processing Magazine |date=January 2008 |url=http://brainimaging.waisman.wisc.edu/publications/2008/DavidsonBuddhaIEEE.pdf |postscript=<!--None--> |deadurl=unfit |archiveurl=https://web.archive.org/web/20120112084117/http://brainimaging.waisman.wisc.edu/publications/2008/DavidsonBuddhaIEEE.pdf |archivedate=12 January 2012 }}</ref><ref>{{cite news |title=Stop meditating, start interacting |author=Chris Frith |newspaper=''[[New Scientist]]'' |date=17 February 2007 |url=http://www.newscientist.com/article/mg19325912.400-stop-meditating-start-interacting.html }}</ref>

===Fitness and exercise===
{{see also|Neurobiological effects of physical exercise#Structural growth}}
Aerobic exercise promotes [[adult neurogenesis]] by increasing the production of [[neurotrophic factors]] (compounds that promote growth or survival of neurons), such as [[brain-derived neurotrophic factor]] (BDNF), [[insulin-like growth factor 1]] (IGF-1), and [[vascular endothelial growth factor]] (VEGF).<ref name="Cerebral hemodynamics and AD">{{cite journal | vauthors = Tarumi T, Zhang R | title = Cerebral hemodynamics of the aging brain: risk of Alzheimer disease and benefit of aerobic exercise | journal = Front Physiol | volume = 5 | issue = | pages = 6 | date = January 2014 | pmid = 24478719 | pmc = 3896879 | doi = 10.3389/fphys.2014.00006 | quote = Exercise-related improvements in brain function and structure may be conferred by the concurrent adaptations in vascular function and structure. Aerobic exercise increases the peripheral levels of growth factors (e.g., BDNF, IFG-1, and VEGF) that cross the blood-brain barrier (BBB) and stimulate neurogenesis and angiogenesis (Trejo et al., 2001; Lee et al., 2002; Fabel et al., 2003; Lopez-Lopez et al., 2004).}}</ref><ref name="BDNF meta analysis">{{cite journal |vauthors=Szuhany KL, Bugatti M, Otto MW | title = A meta-analytic review of the effects of exercise on brain-derived neurotrophic factor | journal = J Psychiatr Res | volume = 60C | issue = | pages = 56–64 | date = October 2014 | pmid = 25455510 | pmc = 4314337 | doi = 10.1016/j.jpsychires.2014.10.003 | quote = Consistent evidence indicates that exercise improves cognition and mood, with preliminary evidence suggesting that brain-derived neurotrophic factor (BDNF) may mediate these effects. The aim of the current meta-analysis was to provide an estimate of the strength of the association between exercise and increased BDNF levels in humans across multiple exercise paradigms. We conducted a meta-analysis of 29 studies (N = 1111 participants) examining the effect of exercise on BDNF levels in three exercise paradigms: (1) a single session of exercise, (2) a session of exercise following a program of regular exercise, and (3) resting BDNF levels following a program of regular exercise. Moderators of this effect were also examined. Results demonstrated a moderate effect size for increases in BDNF following a single session of exercise (Hedges' g = 0.46, p < 0.001). Further, regular exercise intensified the effect of a session of exercise on BDNF levels (Hedges' g = 0.59, p = 0.02). Finally, results indicated a small effect of regular exercise on resting BDNF levels (Hedges' g = 0.27, p = 0.005).&nbsp;... Effect size analysis supports the role of exercise as a strategy for enhancing BDNF activity in humans}}</ref><ref name="Comprehensive review" /> Exercise-induced neurogenesis in the hippocampus is associated with measurable improvements in [[spatial memory]].<ref name="gray matter" /><ref name="BDNF depression">{{cite journal | vauthors = Erickson KI, Miller DL, Roecklein KA | title = The aging hippocampus: interactions between exercise, depression, and BDNF | journal = Neuroscientist | volume = 18 | issue = 1 | pages = 82–97 | year = 2012 | pmid = 21531985 | pmc = 3575139 | doi=10.1177/1073858410397054}}</ref><ref name="Exercise children">{{cite journal |vauthors=Lees C, Hopkins J | title = Effect of aerobic exercise on cognition, academic achievement, and psychosocial function in children: a systematic review of randomized control trials | journal = Prev Chronic Dis | volume = 10 | issue = | pages = E174 | year = 2013 | pmid = 24157077 | pmc = 3809922 | doi = 10.5888/pcd10.130010 }}</ref><ref name="Associated review">{{cite journal | vauthors = Carvalho A, Rea IM, Parimon T, Cusack BJ | title = Physical activity and cognitive function in individuals over 60 years of age: a systematic review | journal = Clin Interv Aging | volume = 9 | issue = | pages = 661–682 | year = 2014 | pmid = 24748784 | pmc = 3990369 | doi = 10.2147/CIA.S55520}}</ref> Consistent aerobic exercise over a period of several months induces marked [[clinically significant]] improvements in [[executive function]] (i.e., the "[[cognitive control]]" of behavior) and increased [[gray matter]] volume in multiple brain regions, particularly those that give rise to cognitive control.<ref name="Comprehensive review">{{cite journal |vauthors=Gomez-Pinilla F, Hillman C | title = The influence of exercise on cognitive abilities | journal = Compr Physiol | volume = 3 | issue = 1 | pages = 403–428 | date = January 2013 | pmid = 23720292 | pmc = 3951958 | doi = 10.1002/cphy.c110063}}</ref><ref name="gray matter">{{cite journal |vauthors=Erickson KI, Leckie RL, Weinstein AM | title = Physical activity, fitness, and gray matter volume | journal = Neurobiol. Aging | volume = 35 Suppl 2 | issue = | pages = S20–528 | date = September 2014 | pmid = 24952993 | pmc = 4094356 | doi = 10.1016/j.neurobiolaging.2014.03.034 |url=http://www.neurobiologyofaging.org/article/S0197-4580(14)00349-2/fulltext | accessdate = 9 December 2014}}</ref><ref name="exercise benefits">{{cite journal |vauthors=Guiney H, Machado L | title = Benefits of regular aerobic exercise for executive functioning in healthy populations | journal = Psychon Bull Rev | volume = 20 | issue = 1 | pages = 73–86 | year = February 2013 | pmid = 23229442 | doi = 10.3758/s13423-012-0345-4 }}</ref><ref name="cognitive control of exercise">{{cite journal |vauthors=Buckley J, Cohen JD, Kramer AF, McAuley E, Mullen SP | title = Cognitive control in the self-regulation of physical activity and sedentary behavior | journal = Front Hum Neurosci | volume = 8 | issue = | page = 747 | year = 2014 | pmid = 25324754 | pmc = 4179677 | doi = 10.3389/fnhum.2014.00747 }}</ref> The brain structures that show the greatest improvements in gray matter volume in response to aerobic exercise are the [[prefrontal cortex]] and [[hippocampus]];<ref name="Comprehensive review" /><ref name="gray matter" /><ref name="BDNF depression" /> moderate improvements are seen in the [[anterior cingulate cortex]], [[parietal cortex]], [[cerebellum]], [[caudate nucleus]], and [[nucleus accumbens]].<ref name="Comprehensive review" /><ref name="gray matter" /><ref name="BDNF depression" /> Higher [[physical fitness]] scores (measured by [[VO2 max|VO<sub>2</sub> max]]) are associated with better executive function, faster processing speed, and greater volume of the hippocampus, caudate nucleus, and nucleus accumbens.<ref name="gray matter" />

===Human echolocation===

[[Human echolocation]] is a learned ability for humans to sense their environment from echoes. This ability is used by some [[blindness|blind]] people to navigate their environment and sense their surroundings in detail. Studies in 2010<ref>{{cite journal | year = 2010 | title = Human Echolocation | url = http://www.journalofvision.org/content/10/7/1050.abstract | journal = Journal of Vision | volume = 10 | issue = 7| page = 1050 | doi=10.1167/10.7.1050}}</ref> and 2011<ref>{{cite journal | year =2011 | title = Neural Correlates of Natural Human Echolocation in Early and Late Blind Echolocation Experts | url = | journal = PLOS ONE | volume = 6| issue = | pages = e20162| doi = 10.1371/journal.pone.0020162 | pmid=21633496 | pmc=3102086 |vauthors=Thaler L, Arnott SR, Goodale MA }}</ref> using [[functional magnetic resonance imaging]] techniques have shown that parts of the brain associated with visual processing are adapted for the new skill of echolocation. Studies with blind patients, for example, suggest that the click-echoes heard by these patients were processed by brain regions devoted to vision rather than audition.<ref>{{cite journal|last=Thaler|first=L|author2=Arnot, S.R. |author3=Goodale, M.A |title=Neural correlates of natural human echolocation in early and late blind echolocation experts|journal=Public Library of Science|year=2011|volume=6|issue=5}}</ref>

===ADHD stimulants===

Reviews of [[magnetic resonance imaging]] (MRI) studies on individuals with ADHD suggest that the long-term treatment of [[attention deficit hyperactivity disorder]] (ADHD) with stimulants, such as [[amphetamine]] or [[methylphenidate]], decreases abnormalities in brain structure and function found in subjects with ADHD, and improves function in several parts of the brain, such as the right [[caudate nucleus]] of the [[basal ganglia]].<ref name="Neuroplasticity 1">{{cite journal |vauthors=Hart H, Radua J, Nakao T, Mataix-Cols D, Rubia K |title=Meta-analysis of functional magnetic resonance imaging studies of inhibition and attention in attention-deficit/hyperactivity disorder: exploring task-specific, stimulant medication, and age effects |journal=JAMA Psychiatry |volume=70 |issue=2 |pages=185–198 |date=February 2013 |pmid=23247506 |doi=10.1001/jamapsychiatry.2013.277 |url=}}</ref><ref name="Neuroplasticity 2">{{cite journal |vauthors=Spencer TJ, Brown A, Seidman LJ, Valera EM, Makris N, Lomedico A, Faraone SV, Biederman J |title=Effect of psychostimulants on brain structure and function in ADHD: a qualitative literature review of magnetic resonance imaging-based neuroimaging studies |journal=J. Clin. Psychiatry |volume=74 |issue=9 |pages=902–917 |date=September 2013 |pmid=24107764 |doi=10.4088/JCP.12r08287 |url= |pmc=3801446}}</ref><ref name="Neuroplasticity 3">{{cite journal | title=Meta-analysis of structural MRI studies in children and adults with attention deficit hyperactivity disorder indicates treatment effects. | journal=Acta psychiatrica Scand. | date=February 2012 | volume=125 | issue=2 | pages=114–126 | pmid=22118249 |vauthors=Frodl T, Skokauskas N | quote = Basal ganglia regions like the right globus pallidus, the right putamen, and the nucleus caudatus are structurally affected in children with ADHD. These changes and alterations in limbic regions like ACC and amygdala are more pronounced in non-treated populations and seem to diminish over time from child to adulthood. Treatment seems to have positive effects on brain structure. | doi=10.1111/j.1600-0447.2011.01786.x}}</ref> Based on studies of [[animal model|rodent models]], the authors of one review proposed that "juvenile exposure to methylphenidate may cause abnormal prefrontal function and impaired plasticity in the healthy brain".<ref name="UrbanGao2013">{{cite journal | vauthors = Urban KR, Gao WJ | title = Methylphenidate and the juvenile brain: enhancement of attention at the expense of cortical plasticity? | journal = Med. Hypotheses | volume = 81 | issue = 6 | pages = 988–994 | date = December 2013 | pmid = 24095262 | pmc = 3851931 | doi = 10.1016/j.mehy.2013.09.009 | url = }}</ref> The same authors noted in another review that in juvenile rats, methylphenidate reduced levels of NR2B subunit of the NMDA receptor without altering NR2A levels in the prefrontal cortex, thereby affecting long-term plasticity in the prefrontal cortex.<ref name="UrbanGao2014">{{cite journal | vauthors = Urban KR, Gao WJ | title = Performance enhancement at the cost of potential brain plasticity: neural ramifications of nootropic drugs in the healthy developing brain | journal = Front. Syst. Neurosci. | volume = 8 | issue = | pages = 38 | year = 2014 | pmid = 24860437 | pmc = 4026746 | doi = 10.3389/fnsys.2014.00038 | url = }}</ref>

===In animals===
{{See also|Brain development|Neural development in humans}}
In a single [[wikt:lifespan|lifespan]], individuals of an animal [[species]] may encounter various changes in brain [[morphology (biology)|morphology]]. Many of these differences are caused by the release of [[hormones]] in the brain; others are the product of [[evolution|evolutionary factors]] or [[Human development (biology)|developmental stages]].<ref name="D.M. Parry 1997 pp. 235">{{cite journal | author = Parry D.M.| year = 1997 | title = Immunocytochemical localization of GnRH precursor in the hypothalamus of European starlings during sexual maturation and photorefractoriness | url = | journal = J. Neuroendocrinol | volume = 9 | issue = | pages = 235–243 | doi=10.1046/j.1365-2826.1997.00575.x|display-authors=etal}}</ref><ref name="D.M. Parry, A.R 1993 pp. 387">D.M. Parry, A.R. Goldsmith Ultrastructural evidence for changes in synaptic input to the hypothalamic luteinizing hormone-releasing hormone neurons in photosensitive and photorefractory starlings ''J. Neuroendocrinol.'', 5 (1993), pp. 387–395</ref><ref name="N.L. Wayne 1998 pp. 356">{{cite journal | author = Wayne N.L.| year = 1998 | title = Seasonal fluctuations in the secretory response of neuroendocrine cells of Aplysia californica to inhibitors of protein kinase A and protein kinase C | url = | journal = Gen. Comp. Endocrinol | volume = 109 | issue = | pages = 356–365 |display-authors=etal | doi=10.1006/gcen.1997.7040}}</ref><ref name="M.A. Hofman, D.F 1992 pp. 257">M.A. Hofman, D.F. Swaab "Seasonal changes in the suprachiasmatic nucleus of man ''Neurosci. Lett.'' 1992; 139 , pp. 257–260</ref> Some changes occur seasonally in species to enhance or generate response behaviors.

====Seasonal brain changes====
Changing brain behavior and morphology to suit other seasonal behaviors is relatively common in animals.<ref name="Science 1981">F. Nottebohm A brain for all seasons: cyclical anatomical changes in song control nuclei of the canary brain Science, 214 (1981), pp. 1368–1370</ref> These changes can improve the chances of mating during breeding season.<ref name="D.M. Parry 1997 pp. 235"/><ref name="D.M. Parry, A.R 1993 pp. 387"/><ref name="N.L. Wayne 1998 pp. 356"/><ref name="Science 1981"/><ref name="S. Takami, A 1984 pp. 253">{{cite journal |author1=Takami S. |author2=Urano A. | year = 1984 | title = The volume of the toad medial amygdala-anterior preoptic complex is sexually dimorphic and seasonally variable | url = | journal = Neurosci. Lett. | volume = 44 | issue = | pages = 253–258 | doi=10.1016/0304-3940(84)90031-4}}</ref><ref name="J.J. Xiong 1997">J.J. Xiong et al. Evidence for seasonal plasticity in the gonadotropin-releasing hormone (GnRH) system of the ewe: Changes in synaptic inputs onto GnRH neurons Endocrinology, 138 (1997), pp. 1240–1250</ref> Examples of seasonal brain morphology change can be found within many classes and species.

Within the class [[Aves]], black-capped chickadees experience an increase in the [[volume]] of their [[hippocampus]] and strength of neural connections to the hippocampus during fall months.<ref>{{cite journal |author1=Barnea A. |author2=Nottebohm F. | year = 1994 | title = Seasonal recruitment of hippocampal neurons in adult free-ranging black-capped chickadees | url = | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 91 | issue = | pages = 11217–11221 | doi=10.1073/pnas.91.23.11217}}</ref><ref>{{cite journal | author = Smulders T.V.| year = 1995 | title = Seasonal variation in hippocampal volume in a food-storing bird, the black-capped chickadee | url = | journal = J. Neurobiol | volume = 27 | issue = | pages = 15–25 | doi=10.1002/neu.480270103|display-authors=etal}}</ref> These morphological changes within the hippocampus which are related to [[spatial memory]] are not limited to birds, as they can also be observed in [[rodents]] and [[amphibians]].<ref name="Science 1981"/> In [[songbirds]], many song control nuclei in the brain increase in size during mating season.<ref name="Science 1981"/> Among birds, changes in brain morphology to influence song patterns, frequency, and volume are common.<ref>{{cite journal | author = Smith G.T. | year = 1996 | title = Seasonal plasticity in the song nuclei of wild rufous-sided towhees | url = | journal = Brain Res. | volume = 734 | issue = | pages = 79–85 | doi=10.1016/0006-8993(96)00613-0}}</ref> [[Gonadotropin-releasing hormone]] (GnRH) [[immunoreactivity]], or the reception of the hormone, is lowered in [[Common starling|European starlings]] exposed to longer periods of light during the day.<ref name="D.M. Parry 1997 pp. 235"/><ref name="D.M. Parry, A.R 1993 pp. 387"/>

The [[California sea hare]], a [[gastropod]], has more successful [[inhibitory postsynaptic potential|inhibition]] of egg-laying hormones outside of mating season due to increased effectiveness of inhibitors in the brain.<ref name="N.L. Wayne 1998 pp. 356"/> Changes to the inhibitory nature of regions of the brain can also be found in humans and other mammals.<ref name="M.A. Hofman, D.F 1992 pp. 257"/> In the amphibian [[Bufo japonicus]], part of the [[amygdala]] is larger before breeding and during [[hibernation]] than it is after breeding.<ref name="S. Takami, A 1984 pp. 253"/>

Seasonal brain variation occurs within many mammals. Part of the hypothalamus of the common [[Sheep|ewe]] is more receptive to GnRH during breeding season than at other times of the year.<ref name="J.J. Xiong 1997"/> [[Humans]] experience a change in the "size of the hypothalamic [[suprachiasmatic nucleus]] and [[vasopressin]]-immunoreactive neurons within it"<ref name="M.A. Hofman, D.F 1992 pp. 257"/> during the [[fall]], when these parts are larger. In the [[spring (season)|spring]], both reduce in size.<ref>Anthony D. Tramontin, Eliot A. Brenowitz "Seasonal plasticity in the adult brain. ''Trends in Neurosciences'', Volume 23, Issue 6, 1 June 2000, Pages 251–258</ref>

====Traumatic brain injury research====

[[Randy Nudo]]'s group found that if a small [[stroke]] (an infarction) is induced by obstruction of blood flow to a portion of a monkey's motor cortex, the part of the body that responds by movement moves when areas adjacent to the damaged brain area are stimulated. In one study, intracortical microstimulation (ICMS) mapping techniques were used in nine normal monkeys. Some underwent ischemic-infarction procedures and the others, ICMS procedures. The monkeys with ischemic infarctions retained more finger flexion during food retrieval and after several months this deficit returned to preoperative levels.<ref name="Frost et al 2003" /> With respect to the distal [[forelimb]] representation, "postinfarction mapping procedures revealed that movement representations underwent reorganization throughout the adjacent, undamaged cortex."<ref name="Frost et al 2003">{{cite journal |last1=Frost |first1=S.B. |last2=Barbay |first2=S. |last3=Friel |first3=K.M. |last4=Plautz |first4=E.J. |last5=Nudo |first5=R.J. |year=2003 |title=Reorganization of Remote Cortical Regions After Ischemic Brain Injury: A Potential Substrate for Stroke Recovery |journal=[[Journal of Neurophysiology]] |volume=89 |issue= 6|pages=3205–3214 |url=http://jn.physiology.org/cgi/reprint/89/6/3205.pdf |doi=10.1152/jn.01143.2002 |pmid=12783955}}</ref> Understanding of interaction between the damaged and undamaged areas provides a basis for better treatment plans in stroke patients. Current research includes the tracking of changes that occur in the motor areas of the cerebral cortex as a result of a stroke. Thus, events that occur in the reorganization process of the brain can be ascertained. Nudo is also involved in studying the treatment plans that may enhance recovery from strokes, such as physiotherapy, [[pharmacotherapy]], and electrical-stimulation therapy.

[[Jon Kaas]], a professor at [[Vanderbilt University]], has been able to show "how somatosensory area 3b and ventroposterior (VP) nucleus of the thalamus are affected by longstanding unilateral dorsal-column lesions at cervical levels in macaque monkeys."<ref name="Jain et al 2008" /> Adult brains have the ability to change as a result of injury but the extent of the reorganization depends on the extent of the injury. His recent research focuses on the somatosensory system, which involves a sense of the body and its movements using many senses. Usually, damage of the somatosensory cortex results in impairment of the body perception. Kaas' research project is focused on how these systems (somatosensory, cognitive, motor systems) respond with plastic changes resulting from injury.<ref name="Jain et al 2008">{{cite journal |last=Jain |first=Neeraj |date=22 October 2008 |title=Large-Scale Reorganization in the Somatosensory Cortex and Thalamus after Sensory Loss in Macaque Monkeys |journal=The Journal of Neuroscience |volume=28 |issue=43 |pages=11042–11060 |publisher= |location= |pmid= 18945912|pmc= 2613515|doi=10.1523/JNEUROSCI.2334-08.2008 |url= |last2=Qi |first2=HX |last3=Collins |first3=CE |last4=Kaas |first4=JH }}</ref>

One recent study of neuroplasticity involves work done by a team of doctors and researchers at [[Emory University]], specifically Dr. [[Donald Stein]]<ref>{{cite web|url=http://www.bme.gatech.edu/facultystaff/faculty_record.php?id=31|archiveurl=https://web.archive.org/web/20080624011530/http://www.bme.gatech.edu/facultystaff/faculty_record.php?id=31|archivedate=2008-06-24 |title=Coulter Department of Biomedical Engineering: BME Faculty |publisher=Bme.gatech.edu |accessdate=12 June 2010}}</ref> and Dr. David Wright. This is the first treatment in 40 years that has significant results in treating traumatic brain injuries while also incurring no known side effects and being cheap to administer.<ref name="stein_interview" /> Dr. Stein noticed that female mice seemed to recover from brain injuries better than male mice, and that at certain points in the [[Estrous cycle|estrus cycle]], females recovered even better. This difference may be attributed to different levels of progesterone, with higher levels of progesterone leading to the faster recovery from brain injury in mice. However, clinical trials showed progesterone offers no significant benefit for traumatic brain injury human patients.<ref>{{Cite web|url=http://news.emory.edu/stories/2014/12/protectiii_results_progesterone_tbi/|title=Progesterone offers no significant benefit in traumatic brain injury clinical trial|date=2014-12-10|website=news.emory.edu|access-date=2016-12-29}}</ref>

== History ==

===Origin===
The term "plasticity" was first applied to behavior in 1890 by [[William James]] in ''[[The Principles of Psychology]]''.<ref name="James 1890" /> The first person to use the term ''neural plasticity'' appears to have been the Polish neuroscientist [[Jerzy Konorski]].<ref name='livingston'>{{cite journal | author = Livingston R.B. | year = 1966 | title = Brain mechanisms in conditioning and learning | url = | journal = Neurosciences Research Program Bulletin | volume = 4 | issue = 3| pages = 349–354 }}</ref><ref name="LeDoux 2002" />

In 1793, Italian anatomist Michele Vicenzo Malacarne described experiments in which he paired animals, trained one of the pair extensively for years, and then dissected both. He discovered that the cerebellums of the trained animals were substantially larger. But these findings were eventually forgotten.<ref>{{cite journal |last1=Rosenzweig |first1=Mark R.|year=1996 |title=Aspects of the search for neural mechanisms of memory |journal=Annual Review of Psychology |volume=47 |pages=1–32 |doi=10.1146/annurev.psych.47.1.1 |pmid=8624134 }}</ref> The idea that the brain and its function are not fixed throughout adulthood was proposed in 1890 by [[William James]] in ''[[The Principles of Psychology]]'', though the idea was largely neglected.<ref name="James 1890" /> Until around the 1970s, neuroscientists believed that brain's structure and function was essentially fixed throughout adulthood.<ref name="Train your brain">Meghan O'Rourke [http://www.slate.com/id/2165040/pagenum/all/#p2 Train Your Brain] 25 April 2007</ref>

The term has since seen broadly applied:
{{quote|Given the central importance of neuroplasticity, an outsider would be forgiven for assuming that it was well defined and that a basic and universal framework served to direct current and future hypotheses and experimentation. Sadly, however, this is not the case. While many neuroscientists use the word neuroplasticity as an umbrella term it means different things to different researchers in different subfields ... In brief, a mutually agreed upon framework does not appear to exist.<ref name="Shaw 2001" />
}}

=== Research and discovery ===

In 1923, [[Karl Lashley]] conducted experiments on [[rhesus monkey]]s that demonstrated changes in neuronal pathways, which he concluded were evidence of plasticity. Despite this, and other research that suggested plasticity took place, neuroscientists did not widely accept the idea of neuroplasticity.

In 1945, [[Justo Gonzalo]] concluded from his research of brain dynamics, that, contrary to the activity of the [[projection areas]], the "central" cortical mass (more or less equidistant from the visual, tactile and auditive projection areas), would be a "maneuvering mass", rather unspecific or multisensory, with capacity to increase neural excitability and re-organize the activity by means of plasticity properties.<ref name=Dinamica>[[Justo Gonzalo|Gonzalo, J]]. (1945, 1950, 1952, 2010). [http://hdl.handle.net/10347/4341 ''Dinámica Cerebral'']. Facsimil edition of Volumen I 1945 and Volumen II 1950 (Madrid: Inst. S. Ramón y Cajal, CSIC), Suplemento I 1952 (Trab. Inst. Cajal Invest. Biol.), first ed. Suplemento II 2010. Santiago de Compostela, Spain: Red Temática en Tecnologías de Computación Artificial/Natural (RTNAC) and Universidad de Santiago de Compostela (USC). {{ISBN|978-84-9887-458-7}}. [http://dspace.usc.es/handle/10347/4341 Open Access]. For a recent review in English see [https://www.novapublishers.com/catalog/product_info.php?products_id=47914 this article (Open Access)].[http://eprints.ucm.es/30931/1/ArticleJG3.pdf English translation of: Article of 1952 and Indexes of Vol. I (1945) and Vol. II (1950), Open Access].</ref> He gives as a first example of adaptation, to see upright with reversing glasses in the [[George M. Stratton|Stratton]] experiment,<ref name=Stratton>{{cite journal | author = Stratton G.M. | authorlink = George M. Stratton | year = 1896 | title = Some preliminary experiments on vision without inversion of the retinal image | url = | journal = Psychological Review | volume = 3 | issue = 6| pages = 611–7 | doi = 10.1037/h0072918 }}</ref> and specially, several first-hand brain injuries cases in which he observed dynamic and adaptive properties in their disorders, in particular in the inverted perception disorder [e.g., see pp 260–62 Vol. I (1945), p 696 Vol. II (1950)].<ref name=Dinamica /> He stated that a sensory signal in a projection area would be only an inverted and constricted outline that would be magnified due to the increase in recruited cerebral mass, and re-inverted due to some effect of brain plasticity, in more central areas, following a spiral growth.<ref name=Grdients>[[Justo Gonzalo|Gonzalo, J.]] (1952). "Las funciones cerebrales humanas según nuevos datos y bases fisiológicas. Una introducción a los estudios de Dinámica Cerebral". [http://aleph.csic.es/F/4KEBKRYX27PBPSNBJBB5AFPQ8THHNR4941PP69A8C6CMG54DBX-15037?func=find-acc&acc_sequence=000501143 ''Trabajos del Inst. Cajal de Investigaciones Biológicas''] '''XLIV''': pp.&nbsp;95–157. [Facsimil edition as `Splemento I´ in [http://hdl.handle.net/10347/4341 ''Dinámica Cerebral'' (2010), Open Access.] [http://eprints.ucm.es/30931/1/ArticleJG3.pdf Complete English translation, Open Access].</ref>

[[Marian Diamond]] of the University of California, Berkeley, produced the first scientific evidence of anatomical brain plasticity, publishing her research in 1964.<ref>{{cite journal | author = Diamond MC, Krech D, Rosenzweig MR | year = 1964 | title = The Effects of an Enriched Environment on the Histology of the Rat Cerebral Cortex | url = http://onlinelibrary.wiley.com/doi/10.1002/cne.901230110/full | journal = J Comp Neurol | volume = 123 | issue = | pages = 111–120 | doi=10.1002/cne.901230110 | pmid=14199261}}</ref><ref name="science.sciencemag.org"/>

Other significant evidence was produced in the 1960s and after, notably from scientists including [[Paul Bach-y-Rita]], [[Michael Merzenich]] along with [[Jon Kaas]], as well as several others.<ref name="Train your brain"/><ref>''Brain Science Podcast'' Episode #10, "Neuroplasticity"</ref>

In the 1960s, [[Paul Bach-y-Rita]] invented a device that was tested on a small number of people, and involved a person sitting in a chair, in which were embedded nubs that were made to vibrate in ways that translated images received in a camera, allowing a form of vision via [sensory substitution]].<ref name="Doidge 2007" /><ref>{{cite web|url=http://www.pbs.org/kcet/wiredscience/video/286-mixed_feelings.html |title=Wired Science . Video: Mixed Feelings |publisher=PBS |accessdate=12 June 2010}}</ref>

Studies in people recovering from [[stroke]] also provided support for neuroplasticity, as regions of the brain remained healthy could sometimes take over, at least in part, functions that had been destroyed; [[Shepherd Ivory Franz]] did work in this area.<ref>{{cite web|url=http://rkthomas.myweb.uga.edu/Franz.htm|archiveurl=https://web.archive.org/web/20120203003746/http://rkthomas.myweb.uga.edu/Franz.htm|archivedate=2012-02-03 |title=Shepherd Ivory Franz |publisher=Rkthomas.myweb.uga.edu |accessdate=12 June 2010}}</ref><ref>{{cite journal|last1=Colotla |first1=Victor A. |last2=Bach-y-Rita |first2=Paul |year=2002 |title=Shepherd Ivory Franz: His contributions to neuropsychology and rehabilitation |journal=Cognitive, Affective & Behavioral Neuroscience |volume=2 |issue=2 |pages=141–148 |url=http://htpprints.yorku.ca/archive/00000236/01/Colotla_Bach-y-Rita_2002.pdf |doi=10.3758/CABN.2.2.141 |deadurl=unfit |archiveurl=https://web.archive.org/web/20120301092815/http://htpprints.yorku.ca/archive/00000236/01/Colotla_Bach-y-Rita_2002.pdf |archivedate=1 March 2012 }}</ref>

[[Eleanor Maguire]] documented changes in hippocampal structure associated with acquiring the knowledge of London's layout in local taxi drivers.<ref name="taxi">{{cite journal | last1 = Maguire | first1 = E. A. | last2 = Frackowiak | first2 = R. S. | last3 = Frith | first3 = C. D. | title = Recalling routes around london: Activation of the right hippocampus in taxi drivers | journal = The Journal of neuroscience : the official journal of the Society for Neuroscience | volume = 17 | issue = 18 | pages = 7103–7110 | year = 1997 | pmid = 9278544 }}</ref><ref name="WoollettMaguire2011">{{cite journal | last1 = Woollett | first1 = K. | last2 = Maguire | first2 = E. A. | title = Acquiring "the Knowledge" of London's Layout Drives Structural Brain Changes | journal = Current Biology | volume = 21 | issue = 24 | pages = 2109–2114 | year = 2011 | pmid = 22169537 | pmc = 3268356 | doi = 10.1016/j.cub.2011.11.018 }}</ref><ref name="MaguireGadian2000">{{cite journal | last1 = Maguire | first1 = E. A. | last2 = Gadian | first2 = D. G. | last3 = Johnsrude | first3 = I. S. | last4 = Good | first4 = C. D. | last5 = Ashburner | first5 = J. | last6 = Frackowiak | first6 = R. S. J. | last7 = Frith | first7 = C. D. | title = Navigation-related structural change in the hippocampi of taxi drivers | journal = Proceedings of the National Academy of Sciences | volume = 97 | issue = 8 | pages = 4398–4403 | year = 2000 | pmid = 10716738 | pmc = 18253 | doi = 10.1073/pnas.070039597 | bibcode = 2000PNAS...97.4398M }}</ref> A redistribution of grey matter was indicated in London Taxi Drivers compared to controls. This work on hippocampal plasticity not only interested scientists, but also engaged the public and media worldwide.

[[Michael Merzenich]] is a neuroscientist who has been one of the pioneers of neuroplasticity for over three decades. He has made some of "the most ambitious claims for the field – that brain exercises may be as useful as drugs to treat diseases as severe as schizophrenia – that plasticity exists from cradle to the grave, and that radical improvements in cognitive functioning – how we learn, think, perceive, and remember are possible even in the elderly."<ref name="Doidge 2007" /> Merzenich's work was affected by a crucial discovery made by [[David Hubel]] and [[Torsten Wiesel]] in their work with kittens. The experiment involved sewing one eye shut and recording the cortical brain maps. Hubel and Wiesel saw that the portion of the kitten's brain associated with the shut eye was not idle, as expected. Instead, it processed visual information from the open eye. It was "…as though the brain didn't want to waste any 'cortical real estate' and had found a way to rewire itself."<ref name="Doidge 2007" />

This implied neuroplasticity during the critical period. However, Merzenich argued that neuroplasticity could occur beyond the critical period. His first encounter with adult plasticity came when he was engaged in a postdoctoral study with Clinton Woosley. The experiment was based on observation of what occurred in the brain when one peripheral nerve was cut and subsequently regenerated. The two scientists micromapped the hand maps of monkey brains before and after cutting a peripheral nerve and sewing the ends together. Afterwards, the hand map in the brain that they expected to be jumbled was nearly normal. This was a substantial breakthrough. Merzenich asserted that, "If the brain map could normalize its structure in response to abnormal input, the prevailing view that we are born with a hardwired system had to be wrong. The brain had to be plastic."<ref name="Doidge 2007" /> Merzenich received the 2016 [[Kavli Prize]] in Neuroscience "for the discovery of mechanisms that allow experience and neural activity to remodel brain function."<ref name="Kavli">http://www.kavliprize.org/prizes-and-laureates/prizes/2016-kavli-prize-neuroscience</ref>

===Notable studies===

[[Hubel]] and [[Torsten Wiesel|Wiesel]] had demonstrated that ocular dominance columns in the lowest neocortical visual area, V1, remained largely immutable after the [[critical period]] in development.<ref name="Hubel et al 1970" /> Researchers also studied critical periods with respect to language; the resulting data suggested that sensory pathways were fixed after the critical period. However, studies determined that environmental changes could alter behavior and cognition by modifying connections between existing neurons and via neurogenesis in the hippocampus and in other parts of the brain, including in the [[cerebellum]].<ref name="Ponti et al 2008" />

Decades of research have shown that substantial changes occur in the lowest neocortical processing areas, and that these changes can profoundly alter the pattern of neuronal activation in response to experience. Neuroscientific research indicates that experience can actually change both the brain's physical structure ([[anatomy]]) and functional organization ([[physiology]]). {{As of | 2014}}{{Citation needed|date=October 2016|reason=This cutoff seems arbitrary without a citation supporting it}}, neuroscientists are engaged in a reconciliation of critical-period studies (demonstrating the immutability of the brain after development) with the more recent research showing how the brain can, and does, change in response to hitherto unsuspected stimuli.<ref name="AirpollutionPhysicalactivity">
{{cite journal
| last = Bos | first = I
| last2 = De Boever | first2 = P
| last3 = Int Panis | first3 = L
| last4 = Meeusen | first4 = R
| title = Physical Activity, Air Pollution and the Brain
| journal = Sports Medicine | volume = 44| issue = | pages = 1505–18| date = August 2014
| url = https://www.researchgate.net/publication/264793941_Physical_Activity_Air_Pollution_and_the_Brain
| doi = 10.1007/s40279-014-0222-6| pmid = 25119155
}}
</ref>
{{trans F}}
== 參見 ==
* [[Activity-dependent plasticity]]
* [[Environmental enrichment (neural)]]
* [[Neural backpropagation]]
* [[Neuroplastic effects of pollution]]
* [[Kinesiology]]
* [[Lumosity]]

==參考資料==
{{Reflist|colwidth=30em
|refs =
<ref name="Pascual-Leone et al. 2011">{{cite journal |author1=Pascual-Leone A. |author2=Freitas C. |author3=Oberman L. |author4=Horvath J. C. |author5=Halko M. |author6=Eldaief M. | year = 2011 | title = Characterizing brain cortical plasticity and network dynamics across the age-span in health and disease with TMS-EEG and TMS-fMRI | url = | journal = Brain Topography | volume = 24 | issue = | pages = 302–315 | doi = 10.1007/s10548-011-0196-8 |display-authors=etal}}</ref>
<ref name="Pascual-Leone et al. 2005">{{cite journal |author1=Pascual-Leone A. |author2=Amedi A. |author3=Fregni F. |author4=Merabet L. B. | year = 2005 | title = The plastic human brain cortex | url = | journal = Annual Review of Neuroscience | volume = 28 | issue = | pages = 377–401 | doi = 10.1146/annurev.neuro.27.070203.144216 }}</ref>
<ref name="Shaw 2001">{{cite book |title=[[Toward a theory of neuroplasticity]] |editor1-last=Shaw|editor1-first=Christopher| editor2-first=Jill| editor2-last=McEachern|year=2001 |publisher=Psychology Press |location=London, England |isbn=978-1-84169-021-6}}</ref>
<ref name="James 1890">"[http://psychclassics.yorku.ca/James/Principles/prin4.htm The Principles of Psychology]", William James 1890, Chapter IV, Habits</ref>
<ref name="LeDoux 2002">{{cite book |title=Synaptic self: how our brains become who we are |last=LeDoux |first=Joseph E. |year=2002 |publisher=Viking |location=New York, United States |isbn=0-670-03028-7 |page=137}}</ref>
<ref name="Rakic 2002">{{cite journal|last = Rakic|first = P.|title = Neurogenesis in adult primate neocortex: an evaluation of the evidence|journal = Nature Reviews Neuroscience|volume = 3|pages =65–71|date= January 2002|doi = 10.1038/nrn700|pmid = 11823806|issue = 1}}</ref>
<ref name="Hubel et al 1970">{{cite journal |last1=Hubel |first1=D.H. |last2=Wiesel |first2=T.N. |date=1 February 1970 |title=The period of susceptibility to the physiological effects of unilateral eye closure in kittens |journal=The Journal of Physiology |volume=206 |issue=2 |pages=419–436 |publisher= |doi= |pmid=5498493 |pmc=1348655}}</ref>
<ref name="Ponti et al 2008">{{cite journal |last1=Ponti |first1=Giovanna |last2=Peretto |first2=Paolo |last3=Bonfanti |first3=Luca |year=2008 |title=Genesis of Neuronal and Glial Progenitors in the Cerebellar Cortex of Peripuberal and Adult Rabbits |journal=PLoS ONE |volume=3 |issue=6 |page= |pages= e2366|publisher= |doi=10.1371/journal.pone.0002366 |pmid=18523645 |pmc=2396292 |last4=Reh |first4=Thomas A. |editor1-last=Reh |editor1-first=Thomas A.}}</ref>
<ref name="Buonomano et al 1998">{{cite journal |last1=Buonomano |first1=Dean V. |authorlink1= |last2=Merzenich |first2=Michael M. |authorlink2=Michael Merzenich |date=March 1998 |title=CORTICAL PLASTICITY: From Synapses to Maps |journal=Annual Review of Neuroscience |volume=21 |series= |issue= |pages=149–186 |at= |publisher= |location= |pmid= 9530495|pmc= |doi=10.1146/annurev.neuro.21.1.149}}</ref>
<ref name="Wall et al 2002">{{cite journal |last1=Wall |first1=J.T. |last2=Xu |first2=J. |last3=Wang |first3=X. |date=September 2002 |title=Human brain plasticity: an emerging view of the multiple substrates and mechanisms that cause cortical changes and related sensory dysfunctions after injuries of sensory inputs from the body |journal=Brain Research Reviews |volume=39 |issue=2–3 |pages=181–215 |publisher=Elsevier Science B.V. |pmid=12423766 |doi=10.1016/S0165-0173(02)00192-3}}</ref>
<ref name="Doidge 2007">{{cite book |title=[[The Brain That Changes Itself|The Brain That Changes Itself: Stories of Personal Triumph from the frontiers of brain science]] |last=Doidge |first=Norman |year=2007 |publisher=Viking |location=New York |isbn=978-0-670-03830-5}}</ref>
<ref name="Merzenich et al 1984">{{cite journal |last1=Merzenich |first1=M.M. |last2=Nelson |first2=R.J. |last3=Stryker |first3=M.P. |last4=Cynader |first4=M.S. |last5=Schoppmann |first5=A. |last6=Zook |first6=J.M. |year=1984 |title=Somatosensory Cortical Map Changes Following Digit Amputation in Adult Monkeys |journal=Journal of Comparative Neurology |volume=224 |issue=4 |pages=591–605|authorlink4=Max Cynader |pmid=6725633 |doi=10.1002/cne.902240408 }}</ref>
}}

==Further reading==
*{{Cite book |editor1-first=Raphael |editor1-last=Pinaud |editor2-first=Liisa A. |editor2-last=Tremere |editor3-first=Peter |editor3-last=De Weerd |title=Plasticity in the visual system: from genes to circuits |url= |edition= |series= |volume= |year=2006 |publisher=Springer |location=New York |isbn=978-0-387-28190-2 |doi=}}
*{{Cite book |editor1-first=Raphael |editor1-last=Pinaud |editor2-first=Liisa A. |editor2-last=Tremere |title=Immediate early genes in sensory processing, cognitive performance and neurological disorders |url= |edition= |series= |volume= |year=2006 |publisher=Springer |location=New York |isbn=978-0-387-33603-9 |doi=}}
*{{Cite news |title=Scans of Monks' Brains Show Meditation Alters Structure, Functioning |first=Sharon |last=Begley |url=http://psyphz.psych.wisc.edu/web/News/Meditation_Alters_Brain_WSJ_11-04.htm |archiveurl=https://web.archive.org/web/20080202012044/http://psyphz.psych.wisc.edu/web/News/Meditation_Alters_Brain_WSJ_11-04.htm |archivedate=2008-02-02 |newspaper=The Wall Street Journal |publisher= |location=Washington D.C. |isbn= |issn= |oclc= |pmid= |pmd= |bibcode= |doi= |id= |date=5 November 2004 |page=B1 |accessdate=}}
*{{Cite journal |last=Donoghue |first=John P. |year=2002 |title=Connecting cortex to machines: recent advances in brain interfaces |journal=Nature Neuroscience |volume=5 |pages=1085–1088 |publisher= |location= |pmc= |doi=10.1038/nn947 |url=http://www.smpp.northwestern.edu/savedLiterature/Donoghue2002NatureNeurosci5p1085.pdf |accessdate=1 February 2010 |pmid=12403992}}
*{{Cite journal | last = Flor | first = H. | date = July 2002 | title = Phantom-limb pain: characteristics, causes, and treatment | journal = The Lancet Neurology | volume = 1 | issue = 3 | pages = 182–189 | publisher = Elsevier | doi = 10.1016/S1474-4422(02)00074-1 }}
*{{Cite journal |last1=Ramachandran |first1=Vilayanur S. |authorlink1=Vilayanur S. Ramachandran |last2=Hirstein |first2=William |year=1998 |title=The perception of phantom limbs. The D. O. Hebb lecture |journal=Brain |volume=121 |issue= 9|pages=1603–1630 |url=http://brain.oxfordjournals.org/cgi/reprint/121/9/1603.pdf |format=PDF |pmid=9762952 |doi= 10.1093/brain/121.9.1603|accessdate=31 January 2010}}
* {{Cite journal |last1=Cohen |first1=Wendy |last2=Hodson |first2=Ann |last3=O'Hare |first3=Anne |last4=Boyle |first4=James |last5=Durrani |first5=Tariq |last6=McCartney |first6=Elspeth |last7=Mattey |first7=Mike |last8=Naftalin |first8=Lionel |last9=Watson |first9=Jocelynne |date=June 2005 |title=Effects of Computer-Based Intervention Through Acoustically Modified Speech (Fast ForWord) in Severe Mixed Receptive-Expressive Language Impairment: Outcomes From a Randomized Controlled Trial |journal=Journal of Speech, Language, and Hearing Research |volume=48 |issue= 3|pages=715–729 |url= |doi=10.1044/1092-4388(2005/049) }}
* {{Cite journal |last=Giszter |first=Simon F. |date=January 2008 |title=SCI: Present and Future Therapeutic Devices and Prostheses |journal=Neurotherapeutics |volume=5 |issue=1 |pages=147–162 |publisher=Elsevier |doi=10.1016/j.nurt.2007.10.062 |url= |language= |pmid=18164494 |pmc=2390875}}
* {{Cite journal |last1=Mahncke |first1=Henry W. |last2=Connor |first2=Bonnie B. |last3=Appelman |first3=Jed |last4=Ahsanuddin |first4=Omar N. |last5=Hardy |first5=Joseph L. |last6=Wood |first6=Richard A. |last7=Joyce |first7=Nicholas M. |last8=Boniske |first8=Tania |last9=Atkins |first9=Sharona M. |last10=Merzenich |first10=M. M. |date=15 August 2006 |title=Memory enhancement in healthy older adults using a brain plasticity-based training program: A randomized, controlled study |journal=Proceedings of the National Academy of Sciences of the United States of America|volume=103 |issue=33 |pages=12523–12528 |publisher= |location= |pmid=16888038 |pmc=1526649 |doi=10.1073/pnas.0605194103 |url= |accessdate=|display-authors=8 }}
* {{Cite journal |last1=Stein |first1=Donald G. |last2=Hoffman |first2=Stuart W. |date=July–August 2003 |title=Concepts of CNS Plasticity in the Context of Brain Damage and Repair |journal=Journal of Head Trauma Rehabilitation |volume=18 |issue=4 |pages=317–341 |publisher= |location= |pmid= 16222128|pmc= |doi= 10.1097/00001199-200307000-00004|url=http://journals.lww.com/headtraumarehab/Fulltext/2003/07000/Concepts_of_CNS_Plasticity_in_the_Context_of_Brain.4.aspx |accessdate=}}
* {{Cite journal|last1= Nudo|first1= Randolph J.|first2= Garrett W.|last2= Milliken|title = Reorganization of Movement Representations in Primary Motor Cortex Following Focal Ischemic Infarct in Adult Squirrel Monkeys|journal =Journal of Neurophysiology|volume= 75 |year = 1996|pages= 2144–149|pmid=8734610|issue=5}}
* {{Cite journal |last1=Wieloch |first1=Tadeusz |last2=Nikolich |first2=Karoly |date=June 2006 |title=Mechanisms of neural plasticity following brain injury |journal=Current Opinion in Neurobiology |volume=16 |issue=3 |pages=258–264 |pmid=16713245 |doi=10.1016/j.conb.2006.05.011 |url= }}

;Videos

*{{Cite video|url = http://neurophilosophy.wordpress.com/2006/10/05/ramachandran-on-concsiousness-mirror-neurons-phantom-limb-sydrome/|title = Phantom Limb Syndrome|author = Ramachandran}} about consciousness, mirror neurons, and phantom limb syndrome

;Other readings

*{{Cite book |title=Rebuilt: how becoming part computer made me more human |last=Chorost |first=Michael |year=2005 |publisher=Houghton Mifflin |location=Boston |isbn=0-618-37829-4}}

==External links==
* {{MeshName|Neuroplasticity}}
*[http://www.edutopia.org/neuroscience-brain-based-learning-myth-busting Neuro Myths: Separating Fact and Fiction in Brain-Based Learning] by Sara Bernard
{{portal|神經科學}}
{{portal|神經科學}}
{{Medicine-stub}}
{{Medicine-stub}}
第10行: 第278行:
[[Category:神经生理学]]
[[Category:神经生理学]]
[[Category:神經內科]]
[[Category:神經內科]]
[[Category:Memory processes]]
[[Category:Neuroplasticity]]
[[Category:Neurophysiology]]
[[Category:Neurotrauma]]
[[Category:Neural networks]]

2017年7月24日 (一) 16:51的版本

神经可塑性(英語:Neuro-plasticity)是指的由于经验原因引起的大脑的结构改变。神经可塑性是近期的发现,过去的科学家往往认为在婴儿关键期后,大脑结构往往不发生变化。 大脑有神经元细胞和神经胶质细胞构成,这些细胞互相连接,通过加强或削弱这些连接,大脑的结构可以发生改变。

參見

參考資料

  1. ^ 1.0 1.1 Livingston R.B. Brain mechanisms in conditioning and learning. Neurosciences Research Program Bulletin. 1966, 4 (3): 349–354. 
  2. ^ 2.0 2.1 Bennett EL, Diamond MC, Krech D, Rosenzweig MR. Chemical and Anatomical Plasticity of the Brain. Science. 1964, 146: 610–619. PMID 14191699. doi:10.1126/science.146.3644.610. 
  3. ^ 3.0 3.1 Rakic, P. Neurogenesis in adult primate neocortex: an evaluation of the evidence. Nature Reviews Neuroscience. January 2002, 3 (1): 65–71. PMID 11823806. doi:10.1038/nrn700. 
  4. ^ Pascual-Leone A.; Amedi A.; Fregni F.; Merabet L. B. The plastic human brain cortex. Annual Review of Neuroscience. 2005, 28: 377–401. doi:10.1146/annurev.neuro.27.070203.144216. 
  5. ^ 5.0 5.1 Pascual-Leone A.; Freitas C.; Oberman L.; Horvath J. C.; Halko M.; Eldaief M.; et al. Characterizing brain cortical plasticity and network dynamics across the age-span in health and disease with TMS-EEG and TMS-fMRI. Brain Topography. 2011, 24: 302–315. doi:10.1007/s10548-011-0196-8. 
  6. ^ Ganguly K, Poo MM. Activity-dependent neural plasticity from bench to bedside. Neuron. October 2013, 80 (3): 729–741. PMID 24183023. doi:10.1016/j.neuron.2013.10.028. 
  7. ^ Keller TA, Just MA. Structural and functional neuroplasticity in human learning of spatial routes. NeuroImage. January 2016, 125: 256–266. PMID 26477660. doi:10.1016/j.neuroimage.2015.10.015. Recent findings with both animals and humans suggest that decreases in microscopic movements of water in the hippocampus reflect short-term neuroplasticity resulting from learning. Here we examine whether such neuroplastic structural changes concurrently alter the functional connectivity between hippocampus and other regions involved in learning. ... These concurrent changes characterize the multidimensionality of neuroplasticity as it enables human spatial learning. 
  8. ^ 8.0 8.1 Doidge, Norman. The Brain that Changes Itself. Penguin Books. 2007: 22. 
  9. ^ Buonomano, Dean V.; Merzenich, Michael M. CORTICAL PLASTICITY: From Synapses to Maps. Annual Review of Neuroscience. March 1998, 21: 149–186. PMID 9530495. doi:10.1146/annurev.neuro.21.1.149. 
  10. ^ Merzenich, M.M.; Nelson, R.J.; Stryker, M.P.; Cynader, M.S.; Schoppmann, A.; Zook, J.M. Somatosensory Cortical Map Changes Following Digit Amputation in Adult Monkeys. Journal of Comparative Neurology. 1984, 224 (4): 591–605. PMID 6725633. doi:10.1002/cne.902240408. 
  11. ^ Wall, J.T.; Xu, J.; Wang, X. Human brain plasticity: an emerging view of the multiple substrates and mechanisms that cause cortical changes and related sensory dysfunctions after injuries of sensory inputs from the body. Brain Research Reviews (Elsevier Science B.V.). September 2002, 39 (2–3): 181–215. PMID 12423766. doi:10.1016/S0165-0173(02)00192-3. 
  12. ^ 12.0 12.1 12.2 12.3 12.4 12.5 Doidge, Norman. The Brain That Changes Itself: Stories of Personal Triumph from the frontiers of brain science. New York: Viking. 2007. ISBN 978-0-670-03830-5. 
  13. ^ Interview with Merzenich, 2004
  14. ^ Draganski et al. "Temporal and Spatial Dynamics of Brain Structure Changes during Extensive Learning" The Journal of Neuroscience, 7 June 2006, 26(23):6314–6317
  15. ^ 15.0 15.1 Ponti, Giovanna; Peretto, Paolo; Bonfanti, Luca; Reh, Thomas A. Reh, Thomas A. , 编. Genesis of Neuronal and Glial Progenitors in the Cerebellar Cortex of Peripuberal and Adult Rabbits. PLoS ONE. 2008, 3 (6): e2366. PMC 2396292可免费查阅. PMID 18523645. doi:10.1371/journal.pone.0002366. 
  16. ^ Young J. A., Tolentino M.; Tolentino. Neuroplasticity and its Applications for Rehabilitation. American Journal of Therapeutics. 2011, 18 (1): 70–80. PMID 21192249. doi:10.1097/MJT.0b013e3181e0f1a4. 
  17. ^ Traumatic Brain Injury (a story of TBI and the results of ProTECT using progesterone treatments) Emory University News Archives
  18. ^ Cutler, Sarah M.; Hoffman, Stuart W.; Pettus, Edward H.; Stein, Donald G. Tapered progesterone withdrawal enhances behavioral and molecular recovery after traumatic brain injury. Experimental Neurology (Elsevier). October 2005, 195 (2): 423–429. PMID 16039652. doi:10.1016/j.expneurol.2005.06.003. 
  19. ^ 19.0 19.1 Stein, Donald. "Plasticity." Personal interview. Alyssa Walz. 19 November 2008.
  20. ^ Progesterone offers no significant benefit in traumatic brain injury clinical trial, Emory University, Atlanta, GA
  21. ^ Dominick M. Maino: Neuroplasticity: Teaching an Old Brain New Tricks, Review of Optometry, January 2009
  22. ^ Indu Vedamurthy; Samuel J. Huang; Dennis M. Levi; Daphne Bavelier; David C. Knill. Recovery of stereopsis in adults through training in a virtual reality task 12 (14). 27 December 2012. doi:10.1167/12.14.53.  |journal=被忽略 (帮助) Article 53
  23. ^ Robert F. Hess; Benjamin Thompson. New insights into amblyopia: binocular therapy and noninvasive brain stimulation 17 (1). February 2013: 89–93. doi:10.1016/j.jaapos.2012.10.018.  |journal=被忽略 (帮助)
  24. ^ 24.0 24.1 Strong GK, Torgerson CJ, Torgerson D, Hulme C. A systematic meta-analytic review of evidence for the effectiveness of the 'Fast ForWord' language intervention program. J Child Psychol Psychiatry. Mar 2011, 52 (3): 224–35. PMC 3061204可免费查阅. PMID 20950285. doi:10.1111/j.1469-7610.2010.02329.x. 
  25. ^ Simons DJ, Boot WR, Charness N, Gathercole SE, Chabris CF, Hambrick DZ, Stine-Morrow EA. Do "Brain-Training" Programs Work? (PDF). Psychological Science in the Public Interest. 2016, 17 (3): 103–186. PMID 27697851. doi:10.1177/1529100616661983. 
  26. ^ Kral A, Sharma A; Sharma. Developmental Neuroplasticity after Cochlear Implantation. Trends Neurosci. 2012, 35 (2): 111–122. PMC 3561718可免费查阅. PMID 22104561. doi:10.1016/j.tins.2011.09.004. 
  27. ^ Kral A, O'Donoghue GM. Profound Deafness in Childhood. New England J Medicine. 2010, 363: 1438–50. PMID 20925546. doi:10.1056/nejmra0911225. 
  28. ^ Beaumont, Geneviève; Mercier, Pierre-Emmanuel; Malouin, Jackson. Decreasing phantom limb pain through observation of action and imagery: A case series. Pain Medicine. 2011, 12 (2): 289–299. PMID 21276185. doi:10.1111/j.1526-4637.2010.01048.x. 
  29. ^ Flor H, Elbert T, Knecht S, Wienbruch C, Pantev C, Birbaumer N; Elbert; Knecht; Wienbruch; Pantev; Birbaumer; Larbig; Taub; et al. Phantom-limb pain as a perceptual correlate of cortical reorganization following arm amputation. Nature. 1995, 375 (6531): 482–484. PMID 7777055. doi:10.1038/375482a0. 
  30. ^ Flor H, Cortical Reorganization And Chronic Pain: Implications For Rehabilitation, J Rehabil Med, 2003, Suppl.41:66–72
  31. ^ Moseley, Brugger, Interdependence of movement and anatomy persists when amputees learn a physiologically impossible movement of their phantom limb, PNAS, 16 September 2009,[1]
  32. ^ Seifert F.; Maihöfner C. Functional and structural imaging of pain-induced neuroplasticity. Current Opinion in Anaesthesiology. 2011, 24: 515–523. doi:10.1097/aco.0b013e32834a1079. 
  33. ^ Maihöfner C.; Handwerker H.O.; Neundorfer B.; Birklein F. Patterns of cortical reorganization in complex regional pain syndrome. Neurology. 2003, 61: 1707–1715. doi:10.1212/01.wnl.0000098939.02752.8e. 
  34. ^ Apkarian A.V., Sosa Y., Sonty S; Sosa; Sonty; Levy; Harden; Parrish; Gitelman; et al. Chronic back pain is associated with decreased prefrontal and thalamic gray matter density. J Neurosci. 2004, 24 (46): 10410–10415. PMID 15548656. doi:10.1523/JNEUROSCI.2541-04.2004. 
  35. ^ Karl A., Birbaumer N., Lutzenberger W.; Birbaumer; Lutzenberger; Cohen; Flor; et al. Reorganization of motor and somatosensory cortex in upper extremity amputees with phantom limb pain. J Neurosci. 2001, 21 (10): 3609–18. PMID 11331390. 
  36. ^ Flor H.; Braun C.; Elbert T.; et al. Extensive reorganization of primary somatosensory cortex in chronic back pain patients. Neurosci Lett. 1997, 224: 5–8. doi:10.1016/s0304-3940(97)13441-3. 
  37. ^ Napadow V., Kettner N., Ryan A.; Kettner; Ryan; Kwong; Audette; Hui; et al. Somatosensory cortical plasticity in carpal tunnel syndrome: a cross-sectional fMRI evaluation. NeuroImage. 2006, 31 (2): 520–530. PMID 16460960. doi:10.1016/j.neuroimage.2005.12.017. 
  38. ^ Pagnoni, Giuseppe; Cekic, Milos. Age effects on gray matter volume and attentional performance in Zen meditation.. Neurobiology of Aging. 28 July 2007, 28 (10): 1623–1627. PMID 17655980. doi:10.1016/j.neurobiolaging.2007.06.008. 
  39. ^ Vestergaard-Poulsen, Peter; van Beek, Martijn; Skewes, Joshua; Bjarkam, Carsten R; Stubberup, Michael; Bertelsen, Jes; Roepstorff, Andreas. Long-term meditation is associated with increased gray matter density in the brain stem.. NeuroReport. 28 January 2009, 20 (2): 170–174. PMID 19104459. doi:10.1097/WNR.0b013e328320012a. 
  40. ^ Luders, Eileen; Toga, Arthur W.; Lepore, Natasha; Gaser, Christian. The underlying anatomical correlates of long-term meditation: larger hippocampal and frontal volumes of gray matter.. NeuroImage. 14 January 2009, 45 (3): 672–678. doi:10.1016/j.neuroimage.2008.12.061. 
  41. ^ Lazar, S.; Kerr, C.; Wasserman, R.; Gray, J.; Greve, D.; Treadway, Michael T.; McGarvey, Metta; Quinn, Brian T.; et al. Meditation experience is associated with increased cortical thickness. NeuroReport. 28 November 2005, 16 (17): 1893–97. PMC 1361002可免费查阅. PMID 16272874. doi:10.1097/01.wnr.0000186598.66243.19. 
  42. ^ Lutz, A.; Greischar, L.L.; Rawlings, N.B.; Ricard, M.; Davidson, R. J. Long-term meditators self-induce high-amplitude gamma synchrony during mental practice. PNAS. 16 November 2004, 101 (46): 16369–73 [8 July 2007]. PMC 526201可免费查阅. PMID 15534199. doi:10.1073/pnas.0407401101. 
  43. ^ Sharon Begley. How Thinking Can Change the Brain. http://www.dalailama.com. 20 January 2007.  外部链接存在于|publisher= (帮助)
  44. ^ Davidson, Richard; Lutz, Antoine. Buddha's Brain: Neuroplasticity and Meditation (PDF). IEEE Signal Processing Magazine. January 2008. 原始内容存档于12 January 2012. 
  45. ^ Chris Frith. Stop meditating, start interacting. New Scientist. 17 February 2007. 
  46. ^ Tarumi T, Zhang R. Cerebral hemodynamics of the aging brain: risk of Alzheimer disease and benefit of aerobic exercise. Front Physiol. January 2014, 5: 6. PMC 3896879可免费查阅. PMID 24478719. doi:10.3389/fphys.2014.00006. Exercise-related improvements in brain function and structure may be conferred by the concurrent adaptations in vascular function and structure. Aerobic exercise increases the peripheral levels of growth factors (e.g., BDNF, IFG-1, and VEGF) that cross the blood-brain barrier (BBB) and stimulate neurogenesis and angiogenesis (Trejo et al., 2001; Lee et al., 2002; Fabel et al., 2003; Lopez-Lopez et al., 2004). 
  47. ^ Szuhany KL, Bugatti M, Otto MW. A meta-analytic review of the effects of exercise on brain-derived neurotrophic factor. J Psychiatr Res. October 2014, 60C: 56–64. PMC 4314337可免费查阅. PMID 25455510. doi:10.1016/j.jpsychires.2014.10.003. Consistent evidence indicates that exercise improves cognition and mood, with preliminary evidence suggesting that brain-derived neurotrophic factor (BDNF) may mediate these effects. The aim of the current meta-analysis was to provide an estimate of the strength of the association between exercise and increased BDNF levels in humans across multiple exercise paradigms. We conducted a meta-analysis of 29 studies (N = 1111 participants) examining the effect of exercise on BDNF levels in three exercise paradigms: (1) a single session of exercise, (2) a session of exercise following a program of regular exercise, and (3) resting BDNF levels following a program of regular exercise. Moderators of this effect were also examined. Results demonstrated a moderate effect size for increases in BDNF following a single session of exercise (Hedges' g = 0.46, p < 0.001). Further, regular exercise intensified the effect of a session of exercise on BDNF levels (Hedges' g = 0.59, p = 0.02). Finally, results indicated a small effect of regular exercise on resting BDNF levels (Hedges' g = 0.27, p = 0.005). ... Effect size analysis supports the role of exercise as a strategy for enhancing BDNF activity in humans 
  48. ^ 48.0 48.1 48.2 48.3 Gomez-Pinilla F, Hillman C. The influence of exercise on cognitive abilities. Compr Physiol. January 2013, 3 (1): 403–428. PMC 3951958可免费查阅. PMID 23720292. doi:10.1002/cphy.c110063. 
  49. ^ 49.0 49.1 49.2 49.3 49.4 Erickson KI, Leckie RL, Weinstein AM. Physical activity, fitness, and gray matter volume. Neurobiol. Aging. September 2014,. 35 Suppl 2: S20–528 [9 December 2014]. PMC 4094356可免费查阅. PMID 24952993. doi:10.1016/j.neurobiolaging.2014.03.034. 
  50. ^ 50.0 50.1 50.2 Erickson KI, Miller DL, Roecklein KA. The aging hippocampus: interactions between exercise, depression, and BDNF. Neuroscientist. 2012, 18 (1): 82–97. PMC 3575139可免费查阅. PMID 21531985. doi:10.1177/1073858410397054. 
  51. ^ Lees C, Hopkins J. Effect of aerobic exercise on cognition, academic achievement, and psychosocial function in children: a systematic review of randomized control trials. Prev Chronic Dis. 2013, 10: E174. PMC 3809922可免费查阅. PMID 24157077. doi:10.5888/pcd10.130010. 
  52. ^ Carvalho A, Rea IM, Parimon T, Cusack BJ. Physical activity and cognitive function in individuals over 60 years of age: a systematic review. Clin Interv Aging. 2014, 9: 661–682. PMC 3990369可免费查阅. PMID 24748784. doi:10.2147/CIA.S55520. 
  53. ^ Guiney H, Machado L. Benefits of regular aerobic exercise for executive functioning in healthy populations. Psychon Bull Rev. February 2013, 20 (1): 73–86. PMID 23229442. doi:10.3758/s13423-012-0345-4. 
  54. ^ Buckley J, Cohen JD, Kramer AF, McAuley E, Mullen SP. Cognitive control in the self-regulation of physical activity and sedentary behavior. Front Hum Neurosci. 2014, 8: 747. PMC 4179677可免费查阅. PMID 25324754. doi:10.3389/fnhum.2014.00747. 
  55. ^ Human Echolocation. Journal of Vision. 2010, 10 (7): 1050. doi:10.1167/10.7.1050. 
  56. ^ Thaler L, Arnott SR, Goodale MA. Neural Correlates of Natural Human Echolocation in Early and Late Blind Echolocation Experts. PLOS ONE. 2011, 6: e20162. PMC 3102086可免费查阅. PMID 21633496. doi:10.1371/journal.pone.0020162. 
  57. ^ Thaler, L; Arnot, S.R.; Goodale, M.A. Neural correlates of natural human echolocation in early and late blind echolocation experts. Public Library of Science. 2011, 6 (5). 
  58. ^ Hart H, Radua J, Nakao T, Mataix-Cols D, Rubia K. Meta-analysis of functional magnetic resonance imaging studies of inhibition and attention in attention-deficit/hyperactivity disorder: exploring task-specific, stimulant medication, and age effects. JAMA Psychiatry. February 2013, 70 (2): 185–198. PMID 23247506. doi:10.1001/jamapsychiatry.2013.277. 
  59. ^ Spencer TJ, Brown A, Seidman LJ, Valera EM, Makris N, Lomedico A, Faraone SV, Biederman J. Effect of psychostimulants on brain structure and function in ADHD: a qualitative literature review of magnetic resonance imaging-based neuroimaging studies. J. Clin. Psychiatry. September 2013, 74 (9): 902–917. PMC 3801446可免费查阅. PMID 24107764. doi:10.4088/JCP.12r08287. 
  60. ^ Frodl T, Skokauskas N. Meta-analysis of structural MRI studies in children and adults with attention deficit hyperactivity disorder indicates treatment effects.. Acta psychiatrica Scand. February 2012, 125 (2): 114–126. PMID 22118249. doi:10.1111/j.1600-0447.2011.01786.x. Basal ganglia regions like the right globus pallidus, the right putamen, and the nucleus caudatus are structurally affected in children with ADHD. These changes and alterations in limbic regions like ACC and amygdala are more pronounced in non-treated populations and seem to diminish over time from child to adulthood. Treatment seems to have positive effects on brain structure. 
  61. ^ Urban KR, Gao WJ. Methylphenidate and the juvenile brain: enhancement of attention at the expense of cortical plasticity?. Med. Hypotheses. December 2013, 81 (6): 988–994. PMC 3851931可免费查阅. PMID 24095262. doi:10.1016/j.mehy.2013.09.009. 
  62. ^ Urban KR, Gao WJ. Performance enhancement at the cost of potential brain plasticity: neural ramifications of nootropic drugs in the healthy developing brain. Front. Syst. Neurosci. 2014, 8: 38. PMC 4026746可免费查阅. PMID 24860437. doi:10.3389/fnsys.2014.00038. 
  63. ^ 63.0 63.1 63.2 Parry D.M.; et al. Immunocytochemical localization of GnRH precursor in the hypothalamus of European starlings during sexual maturation and photorefractoriness. J. Neuroendocrinol. 1997, 9: 235–243. doi:10.1046/j.1365-2826.1997.00575.x. 
  64. ^ 64.0 64.1 64.2 D.M. Parry, A.R. Goldsmith Ultrastructural evidence for changes in synaptic input to the hypothalamic luteinizing hormone-releasing hormone neurons in photosensitive and photorefractory starlings J. Neuroendocrinol., 5 (1993), pp. 387–395
  65. ^ 65.0 65.1 65.2 Wayne N.L.; et al. Seasonal fluctuations in the secretory response of neuroendocrine cells of Aplysia californica to inhibitors of protein kinase A and protein kinase C. Gen. Comp. Endocrinol. 1998, 109: 356–365. doi:10.1006/gcen.1997.7040. 
  66. ^ 66.0 66.1 66.2 M.A. Hofman, D.F. Swaab "Seasonal changes in the suprachiasmatic nucleus of man Neurosci. Lett. 1992; 139 , pp. 257–260
  67. ^ 67.0 67.1 67.2 67.3 F. Nottebohm A brain for all seasons: cyclical anatomical changes in song control nuclei of the canary brain Science, 214 (1981), pp. 1368–1370
  68. ^ 68.0 68.1 Takami S.; Urano A. The volume of the toad medial amygdala-anterior preoptic complex is sexually dimorphic and seasonally variable. Neurosci. Lett. 1984, 44: 253–258. doi:10.1016/0304-3940(84)90031-4. 
  69. ^ 69.0 69.1 J.J. Xiong et al. Evidence for seasonal plasticity in the gonadotropin-releasing hormone (GnRH) system of the ewe: Changes in synaptic inputs onto GnRH neurons Endocrinology, 138 (1997), pp. 1240–1250
  70. ^ Barnea A.; Nottebohm F. Seasonal recruitment of hippocampal neurons in adult free-ranging black-capped chickadees. Proc. Natl. Acad. Sci. U.S.A. 1994, 91: 11217–11221. doi:10.1073/pnas.91.23.11217. 
  71. ^ Smulders T.V.; et al. Seasonal variation in hippocampal volume in a food-storing bird, the black-capped chickadee. J. Neurobiol. 1995, 27: 15–25. doi:10.1002/neu.480270103. 
  72. ^ Smith G.T. Seasonal plasticity in the song nuclei of wild rufous-sided towhees. Brain Res. 1996, 734: 79–85. doi:10.1016/0006-8993(96)00613-0. 
  73. ^ Anthony D. Tramontin, Eliot A. Brenowitz "Seasonal plasticity in the adult brain. Trends in Neurosciences, Volume 23, Issue 6, 1 June 2000, Pages 251–258
  74. ^ 74.0 74.1 Frost, S.B.; Barbay, S.; Friel, K.M.; Plautz, E.J.; Nudo, R.J. Reorganization of Remote Cortical Regions After Ischemic Brain Injury: A Potential Substrate for Stroke Recovery (PDF). Journal of Neurophysiology. 2003, 89 (6): 3205–3214. PMID 12783955. doi:10.1152/jn.01143.2002. 
  75. ^ 75.0 75.1 Jain, Neeraj; Qi, HX; Collins, CE; Kaas, JH. Large-Scale Reorganization in the Somatosensory Cortex and Thalamus after Sensory Loss in Macaque Monkeys. The Journal of Neuroscience. 22 October 2008, 28 (43): 11042–11060. PMC 2613515可免费查阅. PMID 18945912. doi:10.1523/JNEUROSCI.2334-08.2008. 
  76. ^ Coulter Department of Biomedical Engineering: BME Faculty. Bme.gatech.edu. [12 June 2010]. (原始内容存档于2008-06-24). 
  77. ^ Progesterone offers no significant benefit in traumatic brain injury clinical trial. news.emory.edu. 2014-12-10 [2016-12-29]. 
  78. ^ 78.0 78.1 "The Principles of Psychology", William James 1890, Chapter IV, Habits
  79. ^ LeDoux, Joseph E. Synaptic self: how our brains become who we are. New York, United States: Viking. 2002: 137. ISBN 0-670-03028-7. 
  80. ^ Rosenzweig, Mark R. Aspects of the search for neural mechanisms of memory. Annual Review of Psychology. 1996, 47: 1–32. PMID 8624134. doi:10.1146/annurev.psych.47.1.1. 
  81. ^ 81.0 81.1 Meghan O'Rourke Train Your Brain 25 April 2007
  82. ^ Shaw, Christopher; McEachern, Jill (编). Toward a theory of neuroplasticity. London, England: Psychology Press. 2001. ISBN 978-1-84169-021-6. 
  83. ^ 83.0 83.1 Gonzalo, J. (1945, 1950, 1952, 2010). Dinámica Cerebral. Facsimil edition of Volumen I 1945 and Volumen II 1950 (Madrid: Inst. S. Ramón y Cajal, CSIC), Suplemento I 1952 (Trab. Inst. Cajal Invest. Biol.), first ed. Suplemento II 2010. Santiago de Compostela, Spain: Red Temática en Tecnologías de Computación Artificial/Natural (RTNAC) and Universidad de Santiago de Compostela (USC). ISBN 978-84-9887-458-7. Open Access. For a recent review in English see this article (Open Access).English translation of: Article of 1952 and Indexes of Vol. I (1945) and Vol. II (1950), Open Access.
  84. ^ Stratton G.M. Some preliminary experiments on vision without inversion of the retinal image. Psychological Review. 1896, 3 (6): 611–7. doi:10.1037/h0072918. 
  85. ^ Gonzalo, J. (1952). "Las funciones cerebrales humanas según nuevos datos y bases fisiológicas. Una introducción a los estudios de Dinámica Cerebral". Trabajos del Inst. Cajal de Investigaciones Biológicas XLIV: pp. 95–157. [Facsimil edition as `Splemento I´ in Dinámica Cerebral (2010), Open Access. Complete English translation, Open Access.
  86. ^ Diamond MC, Krech D, Rosenzweig MR. The Effects of an Enriched Environment on the Histology of the Rat Cerebral Cortex. J Comp Neurol. 1964, 123: 111–120. PMID 14199261. doi:10.1002/cne.901230110. 
  87. ^ Brain Science Podcast Episode #10, "Neuroplasticity"
  88. ^ Wired Science . Video: Mixed Feelings. PBS. [12 June 2010]. 
  89. ^ Shepherd Ivory Franz. Rkthomas.myweb.uga.edu. [12 June 2010]. (原始内容存档于2012-02-03). 
  90. ^ Colotla, Victor A.; Bach-y-Rita, Paul. Shepherd Ivory Franz: His contributions to neuropsychology and rehabilitation (PDF). Cognitive, Affective & Behavioral Neuroscience. 2002, 2 (2): 141–148. doi:10.3758/CABN.2.2.141. 原始内容存档于1 March 2012. 
  91. ^ Maguire, E. A.; Frackowiak, R. S.; Frith, C. D. Recalling routes around london: Activation of the right hippocampus in taxi drivers. The Journal of neuroscience : the official journal of the Society for Neuroscience. 1997, 17 (18): 7103–7110. PMID 9278544. 
  92. ^ Woollett, K.; Maguire, E. A. Acquiring "the Knowledge" of London's Layout Drives Structural Brain Changes. Current Biology. 2011, 21 (24): 2109–2114. PMC 3268356可免费查阅. PMID 22169537. doi:10.1016/j.cub.2011.11.018. 
  93. ^ Maguire, E. A.; Gadian, D. G.; Johnsrude, I. S.; Good, C. D.; Ashburner, J.; Frackowiak, R. S. J.; Frith, C. D. Navigation-related structural change in the hippocampi of taxi drivers. Proceedings of the National Academy of Sciences. 2000, 97 (8): 4398–4403. Bibcode:2000PNAS...97.4398M. PMC 18253可免费查阅. PMID 10716738. doi:10.1073/pnas.070039597. 
  94. ^ http://www.kavliprize.org/prizes-and-laureates/prizes/2016-kavli-prize-neuroscience
  95. ^ Hubel, D.H.; Wiesel, T.N. The period of susceptibility to the physiological effects of unilateral eye closure in kittens. The Journal of Physiology. 1 February 1970, 206 (2): 419–436. PMC 1348655可免费查阅. PMID 5498493. 
  96. ^ Bos, I; De Boever, P; Int Panis, L; Meeusen, R. Physical Activity, Air Pollution and the Brain. Sports Medicine. August 2014, 44: 1505–18. PMID 25119155. doi:10.1007/s40279-014-0222-6. 

Further reading

Videos
Other readings
  • Chorost, Michael. Rebuilt: how becoming part computer made me more human. Boston: Houghton Mifflin. 2005. ISBN 0-618-37829-4. 

External links