Neurotrophins improve neuromuscular transmission in the adult rat diaphragm

Muscle Nerve. 2004 Mar;29(3):381-6. doi: 10.1002/mus.10558.

Abstract

Neurotrophins modulate acute and sustained synaptic plasticity. In cultured Xenopus laevis neuromuscular junctions, neurotrophins improve neuromuscular transmission. Whether this influence exists at the mammalian neuromuscular junction is unknown. We hypothesized that neurotrophins improve neuromuscular transmission at neuromuscular junctions of adult rat diaphragm muscle fibers. A diaphragm muscle-phrenic nerve preparation was used to determine the effects of brain-derived neurotrophic factor (BDNF), neurotrophin-4 (NT-4) and K252a [tyrosine kinase (Trk) receptor inhibitor] on the extent of neuromuscular transmission failure induced by repetitive nerve stimulation. We found significant enhancement of neuromuscular transmission with BDNF or NT-4 treatment, whereas K252a treatment worsened neuromuscular transmission. In contrast, diaphragm muscle contractile and fatigue properties were unaffected by neurotrophin or K252a treatment. These results demonstrate that BDNF and NT-4 improve synaptic transmission in the adult rat diaphragm muscle, likely in a Trk-dependent fashion. Neurotrophins may constitute a novel therapeutic target to improve neuromuscular function in the diaphragm.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Brain-Derived Neurotrophic Factor / pharmacology
  • Carbazoles / pharmacology
  • Diaphragm / innervation
  • Diaphragm / physiology*
  • Electric Stimulation
  • Enzyme Inhibitors / pharmacology
  • Indole Alkaloids
  • Male
  • Muscle Contraction / drug effects
  • Muscle Contraction / physiology
  • Muscle Fatigue / drug effects
  • Muscle Fatigue / physiology
  • Nerve Growth Factors / pharmacology*
  • Neuromuscular Junction / drug effects*
  • Neuromuscular Junction / physiology
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, trkB / antagonists & inhibitors
  • Receptor, trkB / metabolism
  • Synaptic Transmission / drug effects*
  • Synaptic Transmission / physiology

Substances

  • Brain-Derived Neurotrophic Factor
  • Carbazoles
  • Enzyme Inhibitors
  • Indole Alkaloids
  • Nerve Growth Factors
  • staurosporine aglycone
  • Receptor, trkB
  • neurotrophin 4