Lutfy Kabirullah, Zaveri Nurulain T
Department of Pharmaceutical Sciences, College of Pharmacy, Western University of Health Sciences, Pomona, California, USA.
Astraea Therapeutics, LLC, Mountain View, California, USA.
Prog Mol Biol Transl Sci. 2016;137:149-81. doi: 10.1016/bs.pmbts.2015.10.003. Epub 2015 Dec 23.
Cocaine addiction is a global public health and socioeconomic issue that requires pharmacological and cognitive therapies. Currently there are no FDA-approved medications to treat cocaine addiction. However, in preclinical studies, interventions ranging from herbal medicine to deep-brain stimulation have shown promise for the therapy of cocaine addiction. Recent developments in molecular biology, pharmacology, and medicinal chemistry have enabled scientists to identify novel molecular targets along the pathways involved in drug addiction. In 1994, a receptor that showed a great deal of homology to the traditional opioid receptors was characterized. However, endogenous and exogenous opioids failed to bind to this receptor, which led scientists to name it opioid receptor-like receptor, now referred to as the nociceptin receptor. The endogenous ligand of NOPr was identified a year later and named orphanin FQ/nociceptin. Nociceptin and NOPr are widely distributed throughout the CNS and are involved in many physiological responses, such as food intake, nociceptive processing, neurotransmitter release, etc. Furthermore, exogenous nociceptin has been shown to regulate the activity of mesolimbic dopaminergic neurons, glutamate, and opioid systems, and the stress circuit. Importantly, exogenous nociceptin has been shown to reduce the rewarding and addictive actions of a number of drugs of abuse, such as psychostimulants, alcohol, and opioids. This paper reviews the existing literature on the role of endogenous nociceptin in the rewarding and addictive actions of cocaine. The effect of exogenous nociceptin on these processes is also reviewed. Furthermore, the effects of novel small-molecule NOPr ligands on these actions of cocaine are discussed. Overall, a review of the literature suggests that NOPr could be an emerging target for cocaine addiction pharmacotherapy.
可卡因成瘾是一个全球性的公共卫生和社会经济问题,需要药物治疗和认知疗法。目前尚无美国食品药品监督管理局(FDA)批准的用于治疗可卡因成瘾的药物。然而,在临床前研究中,从草药到深部脑刺激等干预措施已显示出治疗可卡因成瘾的潜力。分子生物学、药理学和药物化学的最新进展使科学家能够确定药物成瘾相关途径中的新分子靶点。1994年,一种与传统阿片受体具有高度同源性的受体被鉴定出来。然而,内源性和外源性阿片类物质均无法与该受体结合,这使得科学家将其命名为阿片受体样受体,现称为孤啡肽受体(NOPr)。一年后,NOPr的内源性配体被鉴定出来,并命名为孤啡肽/痛敏肽。痛敏肽和NOPr广泛分布于整个中枢神经系统,并参与许多生理反应,如食物摄入、痛觉处理、神经递质释放等。此外,外源性痛敏肽已被证明可调节中脑边缘多巴胺能神经元、谷氨酸和阿片系统以及应激回路的活性。重要的是,外源性痛敏肽已被证明可减少多种滥用药物(如精神兴奋剂、酒精和阿片类药物)的奖赏和成瘾作用。本文综述了关于内源性痛敏肽在可卡因奖赏和成瘾作用中作用的现有文献。还综述了外源性痛敏肽对这些过程的影响。此外,还讨论了新型小分子NOPr配体对可卡因这些作用的影响。总体而言,文献综述表明,NOPr可能是可卡因成瘾药物治疗的一个新兴靶点。