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首页> 外文期刊>The European Journal of Neuroscience >BDNF occludes GABA receptor-mediated inhibition of GABA release in rat hippocampal CA1 pyramidal neurons.
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BDNF occludes GABA receptor-mediated inhibition of GABA release in rat hippocampal CA1 pyramidal neurons.

机译:BDNF阻断了大鼠海马CA1锥体神经元中GABA受体介导的GABA释放抑制。

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During the development of the rat hippocampus, both gamma-aminobutyric acid (GABA)(B) autoreceptors and brain-derived neurotrophic factor (BDNF) play important roles in the formation of GABAergic synapses as well as in the GABA(A) receptor-mediated transmissions. While a number of studies have reported rapid effects of BDNF on GABA(A) receptor-mediated responses, the interactions between GABA(B) autoreceptors and BDNF are less clear. Using conventional whole-cell patch-clamp recordings, we demonstrated here that BDNF significantly occludes baclofen-induced suppression of GABA(A) receptor-mediated transmissions in each of the preparations including hippocampal slices prepared from P14 rats, hippocampal CA1 pyramidal neurons isolated from P14 and P21 rats, and cultured hippocampal pyramidal neurons. This effect of BDNF was rapid and reversible, and was mediated via the activation of presynaptic TrkB receptor tyrosine kinases, and subsequent activation of phospholipase C and protein kinase C. On the contrary, in hippocampal CA1 pyramidal neurons isolated from P7 rats, BDNF failed to occlude the GABA(B) receptor-mediated inhibition of GABA release. Thus, the ability of BDNF to occlude the GABA(B) receptor-mediated inhibition of GABA release develops between P7 and P14. This demonstrates a novel aspect of the effects of BDNF on inhibitory transmissions in rat hippocampus, which may have some functional roles in the induction of developmental plasticity and/or pathophysiology of epilepsy.
机译:在大鼠海马的发育过程中,γ-氨基丁酸(GABA)(B)自身受体和脑源性神经营养因子(BDNF)在GABA能突触的形成以及GABA(A)受体介导的过程中均起重要作用传输。尽管许多研究报告了BDNF对GABA(A)受体介导的反应的快速影响,但GABA(B)自体受体与BDNF之间的相互作用尚不清楚。使用常规的全细胞膜片钳记录,我们在这里证明了BDNF在包括从P14大鼠制备的海马切片,从P14分离的海马CA1锥体神经元的每种制剂中BDNF显着地抑制了巴氯芬诱导的GABA(A)受体介导的传递抑制。和P21大鼠,并培养了海马锥体神经元。 BDNF的这种作用是快速且可逆的,并且是通过突触前TrkB受体酪氨酸激酶的激活以及随后的磷脂酶C和蛋白激酶C的激活介导的。相反,在从P7大鼠分离的海马CA1锥体神经元中,BDNF不能阻止GABA(B)受体介导的GABA释放抑制。因此,BDNF阻断GABA(B)受体介导的GABA释放抑制的能力在P7和P14之间发展。这证明了BDNF对大鼠海马中抑制性传递的作用的新方面,其可能在诱发癫痫的发育可塑性和/或病理生理学中具有某些功能性作用。

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