Davies Daryl L, Asatryan Liana, Kuo Sacha T, Woodward John J, King Brian F, Alkana Ronald L, Xiao Cheng, Ye Jiang Hong, Sun Hui, Zhang Li, Hu Xiang-Qun, Hayrapetyan Volodya, Lovinger David M, Machu Tina K
University of Southern California, Los Angeles, California, USA.
Alcohol Clin Exp Res. 2006 Feb;30(2):349-58. doi: 10.1111/j.1530-0277.2006.00023.x.
This report of the proceedings of a symposium presented at the 2005 annual meeting of the Research Society on Alcoholism highlights the actions of ethanol on purinergic (P2XRs) and 5-hydroxytryptamine3 (5-HT3Rs) receptors. Both P2XRs and 5-HT3Rs, are modulated by pharmacologically relevant concentrations of ethanol, with inhibition or stimulation of P2XR subtypes and stimulation of 5-HT3Rs, respectively. With regard to ethanol-modulatory actions, these 2 distinctly different receptor classes have been studied to a much lesser extent than other LGICs. The organizers and chairs were Daryl L. Davies and Tina K. Machu. John J. Woodward discusses the molecular pharmacology and physiology of P2XRs and 5-HT3Rs and sets the stage for a detailed investigation into the ethanol sensitivity of these channels by the invited speakers. Daryl L. Davies discusses the results from recent electrophysiological studies conducted in his and Dr. Woodward's laboratories, highlighting the actions of ethanol on P2XR subtypes. Jiang-Hong Ye discusses results from recent studies using loose-patch and whole-cell recordings on purinergic receptors expressed on neurons from the ventral tegmental area (VTA) in rats. Tina K. Machu discusses electrophysiological studies conducted in her and Dr. David Lovinger's laboratories on nonpore lining residues of the second transmembrane domain (TM2) of the 5-HT3A receptor. Li Zhang presents data demonstrating that F-actin cytoskeletons play a critical role in 5-HT3 receptor clustering in hippocampal neurons. Collectively, the presentations provided strong evidence that P2X and 5-HT3 receptors are important targets for ethanol action.
这份关于在酒精研究学会2005年年会上举办的研讨会会议记录的报告,重点介绍了乙醇对嘌呤能(P2XRs)和5-羟色胺3(5-HT3Rs)受体的作用。P2XRs和5-HT3Rs均受到与药理学相关浓度乙醇的调节,分别表现为对P2XR亚型的抑制或刺激以及对5-HT3Rs的刺激。关于乙醇的调节作用,与其他配体门控离子通道相比,这两类截然不同的受体受到的研究要少得多。组织者和主席分别是达里尔·L·戴维斯和蒂娜·K·马丘。约翰·J·伍德沃德讨论了P2XRs和5-HT3Rs的分子药理学和生理学,并为受邀演讲者对这些通道的乙醇敏感性进行详细研究奠定了基础。达里尔·L·戴维斯讨论了他和伍德沃德博士实验室最近进行的电生理研究结果,重点介绍了乙醇对P2XR亚型的作用。叶江洪讨论了最近使用膜片钳和全细胞记录对大鼠腹侧被盖区(VTA)神经元上表达的嘌呤能受体进行研究的结果。蒂娜·K·马丘讨论了她和大卫·洛文杰博士实验室对5-HT3A受体第二个跨膜结构域(TM2)的非孔衬里残基进行的电生理研究。李章展示的数据表明,F-肌动蛋白细胞骨架在海马神经元中5-HT3受体聚集过程中起关键作用。总的来说这些报告提供了有力证据,表明P2X和5-HT3受体是乙醇作用的重要靶点。