Gilmore Deborah L, Liu Yun, Matsumoto Rae R
Department of Pharmaceutical Sciences, University of Oklahoma Health Sciences Center, P. O. Box 26901, Oklahoma City, OK 73190, USA.
CNS Drug Rev. 2004 Spring;10(1):1-22. doi: 10.1111/j.1527-3458.2004.tb00001.x.
Rimcazole is a carbazole derivative that acts in part as a sigma receptor antagonist. Wellcome Research Laboratories introduced this compound during the 1980s when it was hypothesized to be a novel antipsychotic with an improved side effect profile. However, subsequent clinical trials demonstrated that rimcazole lacked efficacy in schizophrenic patients and it is now primarily used as an experimental tool. In addition to its actions as a sigma receptor antagonist, rimcazole also has high affinity for dopamine transporters, and in recent years it has served as a lead compound for the development of novel dopamine transporter ligands. Although rimcazole cannot be considered a selective ligand for sigma receptors, the recent development of other selective agonists and antagonists for sigma receptors have aided in clarifying the involvement of these receptors in the actions of rimcazole. Many of the physiological and behavioral effects of rimcazole can in fact be ascribed to its action as a sigma receptor antagonist, although there are exceptions. Rimcazole is likely to have a continued role in elucidating sigma receptor function in either in vitro or in vivo systems where sigma receptor-mediated effects can be studied independently of the influence of dopamine and serotonin transporters.
利姆卡唑是一种咔唑衍生物,部分作用为西格玛受体拮抗剂。威康研究实验室在20世纪80年代引入了这种化合物,当时推测它是一种具有改善副作用的新型抗精神病药物。然而,随后的临床试验表明,利姆卡唑对精神分裂症患者缺乏疗效,现在主要用作实验工具。除了作为西格玛受体拮抗剂的作用外,利姆卡唑对多巴胺转运体也有高亲和力,近年来它一直作为新型多巴胺转运体配体开发的先导化合物。尽管利姆卡唑不能被认为是西格玛受体的选择性配体,但最近其他西格玛受体选择性激动剂和拮抗剂的开发有助于阐明这些受体在利姆卡唑作用中的参与情况。事实上,利姆卡唑的许多生理和行为效应可归因于其作为西格玛受体拮抗剂的作用,尽管也有例外。在体外或体内系统中,利姆卡唑可能会在阐明西格玛受体功能方面继续发挥作用,在这些系统中,可以独立于多巴胺和5-羟色胺转运体的影响来研究西格玛受体介导的效应。