An adaptive role for BDNF Val66Met polymorphism in motor recovery in chronic stroke Academic Article uri icon


MeSH Major

  • Brain
  • Brain-Derived Neurotrophic Factor
  • Functional Laterality
  • Polymorphism, Single Nucleotide
  • Recovery of Function
  • Stroke


  • Little is known about the influence of genetic diversity on stroke recovery. One exception is the polymorphism in brain derived neurotrophic factor (BDNF), a critical neurotrophin for brain repair and plasticity. Humans have a high-frequency single nucleotide polymorphism (SNP) in the prodomain of the BDNF gene. Previous studies show that the BDNF Val66Met variant negatively affects motor learning and severity of acute stroke. To investigate the impact of this common BDNF SNP on stroke recovery, we used a mouse model that contains the human BDNF Val66Met variant in both alleles (BDNF(M/M)). Male BDNF(+/+) and BDNF(M/M) littermates received sham or transient middle cerebral artery occlusion. We assessed motor function regularly for 6 months after stroke and then performed anatomical analyses. Despite reported negative association of the SNP with motor learning and acute deficits, we unexpectedly found that BDNF(M/M) mice displayed significantly enhanced motor/kinematic performance in the chronic phase of motor recovery, especially in ipsilesional hindlimb. The enhanced recovery was associated with significant increases in striatum volume, dendritic arbor, and elevated excitatory synaptic markers in the contralesional striatum. Transient inactivation of the contralateral striatum during recovery transiently abolished the enhanced function. This study showed an unexpected benefit of the BDNFVal66Met carriers for functional recovery, involving structural and molecular plasticity in the nonstroked hemisphere. Clinically, this study suggests a role for BDNF genotype in predicting stroke recovery and identifies a novel systems-level mechanism for enhanced motor recovery.

publication date

  • February 14, 2014



  • Academic Article



  • eng

PubMed Central ID

  • PMC3921423

Digital Object Identifier (DOI)

  • 10.1523/JNEUROSCI.4140-13.2014

PubMed ID

  • 24523540

Additional Document Info

start page

  • 2493

end page

  • 502


  • 34


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