Center for Organic and Medicinal Chemistry, Research Triangle Institute , P.O. Box 12194, Research Triangle Park, North Carolina 27709, USA.
J Med Chem. 2013 Mar 28;56(6):2178-95. doi: 10.1021/jm301783x. Epub 2013 Feb 14.
κ opioid receptors (KORs) belong to the G-protein-coupled class of receptors (GPCRs). They are activated by the endogenous opioid peptide dynorphin (DYN) and expressed at particularly high levels within brain areas implicated in modulation of motivation, emotion, and cognitive function. Chronic activation of KORs in animal models has maladaptive effects including increases in behaviors that reflect depression, the propensity to engage in drug-seeking behavior, and drug craving. The fact that KOR activation has such a profound influence on behaviors often triggered by stress has led to interest in selective KOR antagonists as potential therapeutic agents. This Perspective provides a description of preclinical research conducted in the development of several different classes of selective KOR antagonists, a summary of the clinical studies conducted thus far, and recommendations for the type of work needed in the future to determine if these agents would be useful as pharmacotherapies for neuropsychiatric illness.
κ 阿片受体(KOR)属于 G 蛋白偶联受体(GPCR)类。它们被内源性阿片肽强啡肽(DYN)激活,并在与动机、情绪和认知功能调节相关的大脑区域中表达水平特别高。在动物模型中,KOR 的慢性激活具有适应性不良的影响,包括增加反映抑郁的行为、寻求药物的倾向和药物渴望。KOR 激活对经常由应激引发的行为有如此深远的影响,这导致人们对选择性 KOR 拮抗剂作为潜在治疗剂产生了兴趣。本观点提供了对开发几种不同类型的选择性 KOR 拮抗剂的临床前研究的描述,对迄今为止进行的临床研究的总结,以及对未来确定这些药物是否可用作神经精神疾病的药物治疗所需的工作类型的建议。