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The action of BDNF on GABAA currents changes from potentiating to suppressing during maturation of rat hippocampal CA1 pyramidal neurons

机译:BDNF对GABAA电流的作用在大鼠海马CA1锥体神经元成熟期间从增强变为抑制

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摘要

During the development of the hippocampus, the action of GABA shifts from depolarizing to hyperpolarizing, and brain-derived neurotrophic factor (BDNF) has important roles in GABAergic transmission. We demonstrate that BDNF (20 ng ml−1) rapidly and reversibly potentiates postsynaptic GABAA receptor-mediated currents (by 80.5 ± 14.3 %, n = 10) in hippocampal CA1 pyramidal neurons isolated from postnatal day (P)6 rats, using nystatin-perforated patch-clamp recordings. This potentiation is caused by an elevation of intracellular Ca2+ that occurs in response to the activation of Trk B receptor tyrosine kinase and phospholipase C-γ. The modulation of the GABAA responses by BDNF in hippocampal CA1 pyramidal neurons isolated from P10 rats was more diverse (from potentiating to inhibitory), and at P14, BDNF induced a long-lasting inhibition. In addition, Ca2+/calmodulin-dependent protein kinase 2 plays important roles in the potentiating, but not in the inhibitory effect, of BDNF on the GABAA responses. These results suggest that changes in the intracellular signalling pathway could contribute to the developmental shift of the actions of BDNF on inhibitory systems.
机译:在海马的发育过程中,GABA的作用从去极化转变为超极化,并且脑源性神经营养因子(BDNF)在GABA能传递中起重要作用。我们证明了BDNF(20 ng ml-1)快速且可逆地增强了使用制霉菌素从出生后(P)6大鼠分离的海马CA1锥体神经元中突触后GABAA受体介导的电流(通过80.5±14.3%,n = 10)。穿孔膜片钳录音。这种增强作用是由细胞内Ca2 +升高引起的,该升高是由于Trk B受体酪氨酸激酶和磷脂酶C-γ的激活而发生的。 BDNF在从P10大鼠分离的海马CA1锥体神经元中对GABAA反应的调节更为多样(从增强到抑制),并且在P14时,BDNF诱导了长期抑制作用。此外,Ca2 + /钙调蛋白依赖性蛋白激酶2在增强BDNF对GABAA反应的抑制作用中起着重要的作用,但在抑制作用方面不起作用。这些结果表明,细胞内信号传导途径的改变可能有助于BDNF在抑制系统上的作用的发展转移。

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