Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond VA 23298, United States.
Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond VA 23298, United States.
Peptides. 2019 Feb;112:23-31. doi: 10.1016/j.peptides.2018.10.007. Epub 2018 Nov 1.
Intracranial self-stimulation (ICSS) is one procedure that can be used for preclinical abuse potential assessment. In ICSS procedures, subjects with microelectrodes implanted into a brain-reward region are trained to press an operant response lever for pulses of electrical brain stimulation, and drugs are evaluated for their effectiveness to increase or "facilitate" ICSS responding (an abuse-related effect) or to depress ICSS responding (an abuse-limiting effect). ICSS has been used for decades to evaluate determinants of opioid abuse potential, and this article reviews pharmacological and biological determinants of opioid abuse potential as revealed by ICSS studies in rodents. One of the most important observations from ICSS studies is that abused mu opioid receptor (MOR) agonists like morphine often fail to produce abuse-related ICSS facilitation in opioid-naïve subjects, but several days of repeated opioid exposure is sufficient for opioid-induced facilitation to emerge. Future studies with ICSS could help (a) to clarify mechanisms that increase MOR agonist abuse potential during early opioid exposure or during chronic exposure leading to dependence, (b) to evaluate novel opioids either developed as candidate analgesics with reduced abuse potential or identified as designer opioids being synthesized and distributed for illicit use, and (c) to test candidate pharmacotherapies for treatment of opioid abuse in non-dependent and dependent subjects.
颅内自我刺激(ICSS)是一种可用于临床前药物滥用潜力评估的程序。在 ICSS 程序中,将微电极植入大脑奖励区域的动物被训练按压操作性反应杆以获得电脑刺激脉冲,然后评估药物增加或“促进”ICSS 反应(与滥用相关的效果)或抑制 ICSS 反应(限制滥用的效果)的有效性。ICSS 已被使用数十年以评估阿片类药物滥用潜力的决定因素,本文综述了 ICSS 研究在啮齿动物中揭示的阿片类药物滥用潜力的药理学和生物学决定因素。从 ICSS 研究中得到的一个最重要的观察结果是,像吗啡这样被滥用的μ阿片受体(MOR)激动剂通常在阿片类药物-naïve 动物中不能产生与滥用相关的 ICSS 促进作用,但反复几天的阿片类药物暴露足以使阿片类药物诱导的促进作用出现。未来的 ICSS 研究可以帮助(a)阐明在早期阿片类药物暴露期间或导致依赖的慢性暴露期间增加 MOR 激动剂滥用潜力的机制,(b)评估作为候选阿片类药物开发的新型阿片类药物,其具有降低的滥用潜力,或鉴定为合成和分发用于非法用途的设计阿片类药物,以及(c)测试候选药物治疗非依赖和依赖患者的阿片类药物滥用。