Mantilla Carlos B, Zhan Wen-Zhi, Sieck Gary C
Department of Anesthesiology, Mayo Clinic, 200 First Street SW, Rochester, Minnesota 55905, USA.
Muscle Nerve. 2004 Mar;29(3):381-6. doi: 10.1002/mus.10558.
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.
神经营养因子可调节急性和持续性突触可塑性。在培养的非洲爪蟾神经肌肉接头中,神经营养因子可改善神经肌肉传递。这种影响在哺乳动物神经肌肉接头处是否存在尚不清楚。我们推测神经营养因子可改善成年大鼠膈肌纤维神经肌肉接头处的神经肌肉传递。采用膈肌-膈神经标本,以确定脑源性神经营养因子(BDNF)、神经营养因子-4(NT-4)和K252a[酪氨酸激酶(Trk)受体抑制剂]对重复神经刺激诱导的神经肌肉传递失败程度的影响。我们发现,BDNF或NT-4处理可显著增强神经肌肉传递,而K252a处理则会使神经肌肉传递恶化。相比之下,神经营养因子或K252a处理对膈肌的收缩和疲劳特性没有影响。这些结果表明,BDNF和NT-4可改善成年大鼠膈肌的突触传递,可能是以Trk依赖的方式。神经营养因子可能构成改善膈肌神经肌肉功能的新治疗靶点。