Department of Medicinal Chemistry, University of Kansas , 1251 Wescoe Hall Drive, 4070 Malott Hall, Lawrence, Kansas 66045-7572, United States.
J Med Chem. 2013 May 9;56(9):3435-43. doi: 10.1021/jm400388u. Epub 2013 Apr 18.
The neoclerodane diterpene salvinorin A is the major active component of the hallucinogenic mint plant Salvia divinorum Epling and Játiva (Lamiaceae). Since the finding that salvinorin A exerts its potent psychotropic actions through the activation of opioid receptors, the site of action of morphine and related analogues, there has been much interest in elucidating the underlying mechanisms behind its effects. These effects are particularly remarkable because (1) salvinorin A is the first reported non-nitrogenous opioid receptor agonist and (2) its effects are not mediated through the previously investigated targets of psychotomimetics. This Perspective outlines our research program, illustrating a new direction to the development of tools to further elucidate the biological mechanisms of drug tolerance and dependence. The information gained from these efforts is expected to facilitate the design of novel agents to treat pain, drug abuse, and other central nervous system disorders.
新穿心莲烷二萜类化合物 salvinorin A 是迷幻薄荷 Salvia divinorum Epling 和 Játiva(唇形科)的主要活性成分。自从发现 salvinorin A 通过激活阿片受体(吗啡和相关类似物的作用部位)发挥其强大的精神作用以来,人们对阐明其作用背后的潜在机制产生了浓厚的兴趣。这些作用尤其显著,因为 (1) salvinorin A 是第一个报道的非含氮阿片受体激动剂,(2) 其作用不是通过先前研究的精神药物的作用靶点介导的。本观点概述了我们的研究计划,为进一步阐明药物耐受和依赖的生物学机制的工具的开发指明了一个新的方向。从这些努力中获得的信息有望促进设计新型药物来治疗疼痛、药物滥用和其他中枢神经系统疾病。