Ciccocioppo Roberto, Stopponi Serena, Economidou Daina, Kuriyama Makoto, Kinoshita Hiroshi, Heilig Markus, Roberto Marisa, Weiss Friedbert, Teshima Koji
Pharmacology Unit, School of Pharmacy, University of Camerino, Camerino, Italy.
Department II (CNS), Pharmacology Research Laboratories I, Research Division, Mitsubishi Tanabe Pharma Corporation, Yokohama, Japan.
Neuropsychopharmacology. 2014 Oct;39(11):2601-10. doi: 10.1038/npp.2014.113. Epub 2014 Jun 27.
Since its discovery, the nociceptin/orphanin FQ (N/OFQ)-NOP receptor system has been extensively investigated as a promising target to treat alcoholism. Encouraging results obtained with the endogenous ligand N/OFQ stimulated research towards the development of novel brain-penetrating NOP receptor agonists with a pharmacological and toxicological profile compatible with clinical development. Here we describe the biochemical and alcohol-related behavioral effects of the novel NOP receptor agonist MT-7716. MT-7716 has high affinity for human NOP receptors expressed in HEK293 cells with a Ki value of 0.21 nM. MT-7716 concentration-dependently stimulated GTPγ(35)S binding with an EC50 value of 0.30 nM and its efficacy was similar to N/OFQ, suggesting that MT7716 is a full agonist at NOP receptors. In the two bottle choice test MT-7716 (0, 0.3, 1, and 3 mg/kg, bid) given orally for 14 days dose-dependently decreased voluntary alcohol intake in Marchigian Sardinian rats. The effect became gradually stronger following repeated administration, and was still significant 1 week after discontinuation of the drug. Oral naltrexone (30 mg/kg, bid) for 14 days also reduced ethanol intake; however, the effect decreased over the treatment period and rapidly disappeared when drug treatment was discontinued. MT-7716 is also effective for preventing reinstatement caused by both ethanol-associated environmental stimuli and stress. Finally, to investigate the effect of MT-7716 on alcohol withdrawal symptoms, Wistar rats were withdrawn from a 7-day alcohol liquid diet. MT-7716 significantly attenuated somatic alcohol withdrawal symptoms. Together these findings indicate that MT-7716 is a promising candidate for alcoholism treatment remaining effective with chronic administration.
自被发现以来,痛敏肽/孤啡肽FQ(N/OFQ)-NOP受体系统作为治疗酒精中毒的一个有前景的靶点,已得到广泛研究。内源性配体N/OFQ所取得的令人鼓舞的结果激发了对开发具有与临床开发相兼容的药理学和毒理学特征的新型脑渗透性NOP受体激动剂的研究。在此,我们描述新型NOP受体激动剂MT-7716的生化及与酒精相关的行为学效应。MT-7716对在HEK293细胞中表达的人NOP受体具有高亲和力,其Ki值为0.21 nM。MT-7716浓度依赖性地刺激GTPγ(35)S结合,EC50值为0.30 nM,其效能与N/OFQ相似,表明MT7716是NOP受体的完全激动剂。在双瓶选择试验中,给Marchigian撒丁岛大鼠口服MT-7716(0、0.3、1和3 mg/kg,每日两次),持续14天,剂量依赖性地降低了其自愿酒精摄入量。重复给药后,这种效应逐渐增强,停药1周后仍很显著。口服纳曲酮(30 mg/kg,每日两次),持续14天,也减少了乙醇摄入量;然而,这种效应在治疗期间逐渐减弱,停药后迅速消失。MT-7716对预防由乙醇相关环境刺激和应激引起的复吸也有效。最后,为了研究MT-7716对酒精戒断症状的影响,将Wistar大鼠从7天的酒精液体饮食中撤药。MT-7716显著减轻了躯体酒精戒断症状。这些研究结果共同表明,MT-7716是治疗酒精中毒的一个有前景的候选药物,长期给药仍有效。