Albert P R, Lembo P, Storring J M, Charest A, Saucier C
Department of Pharmacology and Therapeutics, McGill University, Montreal, Canada.
Neuropsychopharmacology. 1996 Jan;14(1):19-25. doi: 10.1016/S0893-133X(96)80055-8.
The hypothesis that antianxiety or antidepressant agents (e.g., 5-HT1A agonists, 5-HT uptake blockers) exert their clinical actions via enhancement of serotonergic neurotransmission due to desensitization of 5-HT1A autoreceptors predicts that regulation of this receptor plays a crucial role in the therapeutic actions of these agents. A multidisciplinary strategy is described for the characterization of the 5-HT1A receptor at the level of cellular signaling mechanisms and genetic regulation, using heterologous expression of the cloned receptor in cell lines, site-directed mutagenesis, isolation of receptor-positive neuronal cell lines, and promoter analysis of the 5-HT1A receptor gene. These analyses will yield new insights into the possible mechanisms down-regulation of 5-HT1A receptor signaling, and may suggest novel sites of inherent defect involved in anxiety syndromes or major depression.
抗焦虑或抗抑郁药(如5-HT1A激动剂、5-HT摄取阻滞剂)通过5-HT1A自身受体脱敏增强5-羟色胺能神经传递而发挥临床作用的假说预测,该受体的调节在这些药物的治疗作用中起关键作用。本文描述了一种多学科策略,用于在细胞信号传导机制和基因调控水平上对5-HT1A受体进行表征,包括在细胞系中克隆受体的异源表达、定点诱变、分离受体阳性神经元细胞系以及对5-HT1A受体基因的启动子分析。这些分析将为5-HT1A受体信号下调的可能机制提供新的见解,并可能提示焦虑综合征或重度抑郁症所涉及的内在缺陷的新位点。