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大鼠丘脑网状核和中继神经元中GABAA受体介导的氯离子电流

GABAA receptor-mediated Cl- currents in rat thalamic reticular and relay neurons.

作者信息

Zhang S J, Huguenard J R, Prince D A

机构信息

Department of Neurology and Neurological Sciences, Stanford University Medical Center, Stanford, California 94305, USA.

出版信息

J Neurophysiol. 1997 Nov;78(5):2280-6. doi: 10.1152/jn.1997.78.5.2280.

Abstract

GABAA receptor-mediated Cl- currents in rat thalamic reticular and relay neurons. J. Neurophysiol. 78: 2280-2286, 1997. Spontaneous and evoked inhibitory postsynaptic currents (sIPSCs and eIPSCs) and responses to exogenously applied gamma-aminobutyric acid (GABA), mediated by GABA type A (GABAA) receptors, were recorded in inhibitory neurons of nucleus reticularis thalami (nRt) and their target relay cells in ventrobasal (VB) nuclei by using patch clamp techniques in rat thalamic slices. The decay of sIPSCs in both nRt and VB neurons was best fitted with two exponential components. The decay time constants of sIPSCs in nRt neurons were much slower (tau1 = 38 ms; tau2 = 186 ms) than those previously reported in a variety of preparations and two to three times slower than those in VB neurons (tau1 = 17 ms; tau2 = 39 ms). GABAA receptor-mediated Cl- currents directly evoked by local GABA application also had a much slower decay time constant in nRt (225 ms) than in VB neurons (115 ms). Slow decay of GABA responses enhances the efficacy of recurrent intranuclear inhibition in nRt. The results suggest a functional diversity of GABAA receptors that may relate to the known heterogeneity of GABAA receptor subunits in these two thalamic nuclei.

摘要

大鼠丘脑网状核和中继神经元中GABAA受体介导的氯离子电流。《神经生理学杂志》78: 2280 - 2286, 1997年。采用膜片钳技术在大鼠丘脑切片中记录丘脑网状核(nRt)抑制性神经元及其腹侧基底核(VB)中靶中继细胞的由A型γ-氨基丁酸(GABAA)受体介导的自发性和诱发性抑制性突触后电流(sIPSCs和eIPSCs)以及对外源性施加的γ-氨基丁酸(GABA)的反应。nRt和VB神经元中sIPSCs的衰减最适合用两个指数成分来拟合。nRt神经元中sIPSCs的衰减时间常数比之前在各种标本中报道的要慢得多(τ1 = 38毫秒;τ2 = 186毫秒),比VB神经元中的慢两到三倍(τ1 = 17毫秒;τ2 = 39毫秒)。局部施加GABA直接诱发的GABAA受体介导的氯离子电流在nRt中的衰减时间常数(225毫秒)也比VB神经元中的慢得多(115毫秒)。GABA反应的缓慢衰减增强了nRt中核内反复抑制的效能。结果表明GABAA受体存在功能多样性,这可能与这两个丘脑核中已知的GABAA受体亚基异质性有关。

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