Helal Mohamed A, Habib Eman S, Chittiboyina Amar G
Biomedical Sciences Program, University of Science and Technology, Zewail City of Science and Technology, Giza 12588, Egypt; Department of Medicinal Chemistry, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
Eur J Med Chem. 2017 Dec 1;141:632-647. doi: 10.1016/j.ejmech.2017.10.012. Epub 2017 Oct 10.
Kappa opioid receptor (KOP) is a G-protein coupled receptor mainly expressed in the cerebral cortex and hypothalamus. It is implicated in nociception, diuresis, emotion, cognition, and immune system functions. KOP agonists possess a strong analgesic effect accompanied by a feeling of dysphoria. On the other hand, antagonists of this receptor were found to block depression, anxiety, and drug-seeking behaviors in animal models. Recently, great interest has been given to the development of selective KOP antagonists as an addiction treatment that does not cause dependence itself or show high relapse rates like the currently used agents. This review provides a comprehensive survey of the KOP antagonists developed for this purpose together with their in vivo studies and clinical trials. In addition, a future perspective and recommendations for the work needed to develop clinically relevant KOP antagonists are presented.
κ-阿片受体(KOP)是一种主要在大脑皮层和下丘脑表达的G蛋白偶联受体。它与痛觉感受、利尿、情绪、认知和免疫系统功能有关。KOP激动剂具有强烈的镇痛作用,并伴有烦躁不安的感觉。另一方面,在动物模型中发现该受体的拮抗剂可阻断抑郁、焦虑和觅药行为。最近,人们对开发选择性KOP拮抗剂作为一种成瘾治疗方法产生了极大兴趣,这种方法本身不会导致依赖,也不会像目前使用的药物那样显示出高复发率。本综述全面概述了为此目的开发的KOP拮抗剂及其体内研究和临床试验。此外,还提出了未来的展望以及开发临床相关KOP拮抗剂所需工作的建议。