The BDNF Val66Met polymorphism impairs NMDA receptor-dependent synaptic plasticity in the hippocampus. Academic Article uri icon

Overview

abstract

  • The Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene results in a defect in regulated release of BDNF and affects episodic memory and affective behaviors. However, the precise role of the BDNF Val66Met polymorphism in hippocampal synaptic transmission and plasticity has not yet been studied. Therefore, we examined synaptic properties in the hippocampal CA3-CA1 synapses of BDNF(Met/Met) mice and matched wild-type mice. Although basal glutamatergic neurotransmission was normal, both young and adult mice showed a significant reduction in NMDA receptor-dependent long-term potentiation. We also found that NMDA receptor-dependent long-term depression was decreased in BDNF(Met/Met) mice. However, mGluR-dependent long-term depression was not affected by the BDNF Val66Met polymorphism. Consistent with the NMDA receptor-dependent synaptic plasticity impairment, we observed a significant decrease in NMDA receptor neurotransmission in the CA1 pyramidal neurons of BDNF(Met/Met) mice. Thus, these results show that the BDNF Val66Met polymorphism has a direct effect on NMDA receptor transmission, which may account for changes in synaptic plasticity in the hippocampus.

publication date

  • June 30, 2010

Research

keywords

  • Brain-Derived Neurotrophic Factor
  • Hippocampus
  • Neuronal Plasticity
  • Neurons
  • Receptors, N-Methyl-D-Aspartate
  • Synapses

Identity

PubMed Central ID

  • PMC2911131

Scopus Document Identifier

  • 77954421126

Digital Object Identifier (DOI)

  • 10.1523/JNEUROSCI.1405-10.2010

PubMed ID

  • 20592208

Additional Document Info

volume

  • 30

issue

  • 26