Förstera Benjamin, Castro Patricio A, Moraga-Cid Gustavo, Aguayo Luis G
Laboratory of Neurophysiology, Department of Physiology, University of Concepcion Concepcion, Chile.
Laboratory of Environmental Neurotoxicology, Department of Biomedical Sciences, Faculty of Medicine, Universidad Católica del Norte Coquimbo, Chile.
Front Cell Neurosci. 2016 May 6;10:114. doi: 10.3389/fncel.2016.00114. eCollection 2016.
In recent years there has been an increase in the understanding of ethanol actions on the type A γ-aminobutyric acid chloride channel (GABAAR), a member of the pentameric ligand gated ion channels (pLGICs). However, the mechanism by which ethanol potentiates the complex is still not fully understood and a number of publications have shown contradictory results. Thus many questions still remain unresolved requiring further studies for a better comprehension of this effect. The present review concentrates on the involvement of GABAAR in the acute actions of ethanol and specifically focuses on the immediate, direct or indirect, synaptic and extra-synaptic modulatory effects. To elaborate on the immediate, direct modulation of GABAAR by acute ethanol exposure, electrophysiological studies investigating the importance of different subunits, and data from receptor mutants will be examined. We will also discuss the nature of the putative binding sites for ethanol based on structural data obtained from other members of the pLGICs family. Finally, we will briefly highlight the glycine gated chloride channel (GlyR), another member of the pLGIC family, as a suitable target for the development of new pharmacological tools.
近年来,人们对乙醇作用于A型γ-氨基丁酸氯离子通道(GABAAR)的认识有所增加,GABAAR是五聚体配体门控离子通道(pLGICs)家族的一员。然而,乙醇增强该复合体的机制仍未完全阐明,许多出版物显示出相互矛盾的结果。因此,许多问题仍未解决,需要进一步研究以更好地理解这种效应。本综述集中于GABAAR在乙醇急性作用中的参与情况,并特别关注直接或间接的即时突触和突触外调节作用。为详细阐述急性乙醇暴露对GABAAR的直接即时调节作用,将研究探讨不同亚基重要性的电生理研究以及来自受体突变体的数据。我们还将基于从pLGICs家族其他成员获得的结构数据,讨论乙醇假定结合位点的性质。最后,我们将简要强调甘氨酸门控氯离子通道(GlyR),pLGIC家族的另一个成员,作为开发新药理学工具的合适靶点。