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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Repetitive Transcranial Magnetic Stimulation Enhances BDNF-TrkB Signaling in Both Brain and Lymphocyte.
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Repetitive Transcranial Magnetic Stimulation Enhances BDNF-TrkB Signaling in Both Brain and Lymphocyte.

机译:重复经颅磁刺激增强脑和淋巴细胞中的BDNF-TrkB信号。

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摘要

Repetitive transcranial magnetic stimulation (rTMS) induces neuronal long-term potentiation or depression. Although brain-derived neurotrophic factor (BDNF) and its cognate tyrosine receptor kinase B (TrkB) contribute to the effects of rTMS, their precise role and underlying mechanism remain poorly understood. Here we show that daily 5 Hz rTMS for 5 d improves BDNF-TrkB signaling in rats by increasing the affinity of BDNF for TrkB, which results in higher tyrosine-phosphorylated TrkB, increased recruitment of PLC-gamma1 and shc/N-shc to TrkB, and heightened downstream ERK2 and PI-3K activities in prefrontal cortex and in lymphocytes. The elevated BDNF-TrkB signaling is accompanied by an increased association between the activated TrkB and NMDA receptor (NMDAR). In normal human subjects, 5 d rTMS to motor cortex decreased resting motor threshold, which correlates with heightened BDNF-TrkB signaling and intensified TrkB-NMDAR association in lymphocytes. These findings suggest that rTMS to cortex facilitates BDNF-TrkB-NMDAR functioning in both cortex and lymphocytes.
机译:反复经颅磁刺激(rTMS)诱导神经元长期增强或抑制。尽管脑源性神经营养因子(BDNF)及其相关的酪氨酸受体激酶B(TrkB)有助于rTMS的作用,但它们的确切作用和潜在机制仍知之甚少。在这里,我们显示每天5 Hz rTMS 5天可通过增加BDNF对TrkB的亲和力来改善大鼠BDNF-TrkB信号传导,从而导致酪氨酸磷酸化的TrkB更高,PLC-gamma1和shc / N-shc对TrkB的募集增加,并增加额叶前皮质和淋巴细胞的下游ERK2和PI-3K活性。升高的BDNF-TrkB信号传导伴随着活化的TrkB与NMDA受体(NMDAR)之间的缔合增加。在正常人中,运动皮层5 d rTMS降低了静息运动阈,这与淋巴细胞中BDNF-TrkB信号转导升高和TrkB-NMDAR缔合增强有关。这些发现表明,rTMS皮层促进BDNF-TrkB-NMDAR在皮层和淋巴细胞中的功能。

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