A role for BDNF in the late-phase of hippocampal long-term potentiation

Neuropharmacology. 1998 Apr-May;37(4-5):553-9. doi: 10.1016/s0028-3908(98)00035-5.

Abstract

The neurotrophin family of growth factors has received enormous attention recently for its role in modulating synaptic strength in the developing and adult nervous system. Several recent studies have indicated a role for brain-derived neurotrophic factor (BDNF) in long-term potentiation (LTP), a form of long-lasting plasticity observed at synapses in the hippocampus and other brain areas. The late-phase (L-LTP; e.g. > 2 h) of LTP has been shown to require the synthesis of new proteins. We have examined whether BDNF or other TrkB ligands participate in L-LTP in two ways: by examining transgenic mice which lack BDNF or by acutely blocking TrkB function using function-blocking antibodies. Slices from BDNF knock-out animals or slices treated with TrkB antibodies failed to exhibit L-LTP, indicating that TrkB ligands participate in extending synaptic enhancement from a short-lasting to a long-lasting form.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain-Derived Neurotrophic Factor / physiology*
  • Hippocampus / cytology
  • Hippocampus / physiology*
  • Immune Sera / metabolism
  • Immunoglobulin G / metabolism
  • In Vitro Techniques
  • Long-Term Potentiation / drug effects
  • Long-Term Potentiation / physiology*
  • Male
  • Membrane Potentials / drug effects
  • Mice
  • Mice, Knockout
  • Protein Binding / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Receptor, Ciliary Neurotrophic Factor
  • Receptors, Nerve Growth Factor / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Fusion Proteins / pharmacology

Substances

  • Brain-Derived Neurotrophic Factor
  • Immune Sera
  • Immunoglobulin G
  • Receptor, Ciliary Neurotrophic Factor
  • Receptors, Nerve Growth Factor
  • Recombinant Fusion Proteins
  • Receptor Protein-Tyrosine Kinases