首页> 外文期刊>Alcohol and alcoholism: international journal of the Medical Council on Alcoholism >Ethanol increases GABAergic transmission and excitability in cerebellar molecular layer interneurons from GAD67-GFP knock-in mice.
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Ethanol increases GABAergic transmission and excitability in cerebellar molecular layer interneurons from GAD67-GFP knock-in mice.

机译:乙醇会增加GAD67-GFP敲入小鼠的小脑分子层间神经元的GABA能传递和兴奋性。

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AIMS: This study assessed the acute effect of ethanol on GABAergic transmission at molecular layer interneurons (MLIs; i.e. basket and stellate cells) in the cerebellar cortex. The actions of ethanol on spontaneous firing of these pacemaker neurons were also measured. METHODS: Transgenic mice (glutamic acid-decarboxylase 67-green fluorescent protein knock-in mice) that express green fluorescence protein in GABAergic interneurons were used to aid in the identification of MLIs. Parasagittal cerebellar slices were prepared and whole-cell patch-clamp electrophysiological techniques were used to measure GABA(A) receptor-mediated spontaneous and miniature inhibitory postsynaptic currents (sIPSCs and mIPSCs). Loose-seal cell-attached recordings were used to measure spontaneous action potential firing. RESULTS: Stellate cells received spontaneous GABAergic input in the form of a mixture of action potential-dependent events (sIPSCs) and quantal events (mIPSCs); ethanol increased sIPSC frequency to a greater extent than mIPSC frequency. Ethanol increased spontaneous action potential firing of MLIs, which could explain the increase in sIPSC frequency in stellate cells. Basket cells received GABAergic input in the form of quantal events only. Ethanol significantly increased the frequency of these events, which may be mediated by a different type of interneuron (perhaps, the Lugaro cell) or Purkinje cell collaterals. CONCLUSIONS: Ethanol exposure differentially increases GABA release at stellate cell vs. basket cell-to-Purkinje cell synapses. This effect may contribute to the abnormalities in cerebellar function associated with alcohol intoxication.
机译:目的:这项研究评估了乙醇对小脑皮层分子中层神经元(MLIs;即篮和星状细胞)GABA能传递的急性影响。还测量了乙醇对这些起搏器神经元自发放电的作用。方法:使用在GABA能中间神经元中表达绿色荧光蛋白的转基因小鼠(谷氨酸脱羧酶67-绿色荧光蛋白敲入小鼠)来辅助MLI的鉴定。准备矢状旁矢状小脑切片,并使用全细胞膜片钳电生理技术测量GABA(A)受体介导的自发和微型抑制性突触后电流(sIPSC和mIPSC)。贴有松密封的细胞的记录用于测量自发动作电位放电。结果:星状细胞以动作电位依赖性事件(sIPSCs)和定量事件(mIPSCs)的混合物形式接受自发的GABA能输入;乙醇增加sIPSC频率的幅度大于mIPSC频率。乙醇增加了MLI的自发动作电位放电,这可以解释星状细胞中sIPSC频率的增加。篮状细胞仅以数量事件的形式接受GABA能输入。乙醇显着增加了这些事件的发生频率,这可能是由不同类型的中间神经元(可能是Lugaro细胞)或Purkinje细胞侧支介导的。结论:暴露于星状细胞与篮细胞对普金野细胞的突触相比,乙醇暴露差异地增加了GABA的释放。这种作用可能导致与酒精中毒有关的小脑功能异常。

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