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Effects of neuronal nicotinic acetylcholine receptor allosteric modulators in animal behavior studies

机译:神经元烟碱型乙酰胆碱受体变构调节剂在动物行为研究中的作用

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Nicotinic acetylcholine receptors (nAChRs) are ligand-gated cation-conducting transmembrane channels from the cys-loop receptor superfamily. The neuronal subtypes of these receptors (e.g. the α7 and α4β2 subtypes) are involved in neurobehavioral processes such as anxiety, the central processing of pain, food intake, nicotine seeking behavior, and a number of cognitive functions like learning and memory. Neuronal nAChR dysfunction is involved in the pathophysiology of many neurological disorders, and behavioral studies in animals are useful models to assess the effects of compounds that act on these receptors. Allosteric modulators are ligands that bind to the receptors at sites other than the orthosteric site where acetylcholine, the endogenous agonist for the nAChRs, binds. While conventional ligands for the neuronal nAChRs have been studied for their behavioral effects in animals, allosteric modulators for these receptors have only recently gained attention, and research on their behavioral effects is growing rapidly. Here we will discuss the behavioral effects of allosteric modulators of the neuronal nAChRs.
机译:烟碱乙酰胆碱受体(nAChRs)是来自cys-loop受体超家族的配体门控的阳离子传导跨膜通道。这些受体的神经元亚型(例如α7和α4β2亚型)涉及神经行为过程,例如焦虑,疼痛的中枢处理,食物摄入,尼古丁寻求行为以及许多认知功能,例如学习和记忆。神经元nAChR功能障碍与许多神经系统疾病的病理生理有关,动物行为研究是评估作用于这些受体的化合物作用的有用模型。变构调节剂是在正构位点以外的位点与受体结合的配体,乙酰正胆碱是nAChRs的内源性激动剂。虽然已经研究了神经元nAChRs的常规配体在动物中的行为效应,但这些受体的变构调节剂只是最近才引起人们的注意,其行为效应的研究也在迅速发展。在这里,我们将讨论神经元nAChRs的变构调节剂的行为效应。

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