Molecular Targets and Medications Discovery Branch, National Institute on Drug Abuse Intramural Research Program, National Institutes of Health, Baltimore, Maryland 21224, USA; email:
Annu Rev Pharmacol Toxicol. 2021 Jan 6;61:609-628. doi: 10.1146/annurev-pharmtox-030220-124205.
The abuse of illicit psychostimulants such as cocaine and methamphetamine continues to pose significant health and societal challenges. Despite considerable efforts to develop medications to treat psychostimulant use disorders, none have proven effective, leaving an underserved patient population and unanswered questions about what mechanism(s) of action should be targeted for developing pharmacotherapies. As both cocaine and methamphetamine rapidly increase dopamine (DA) levels in mesolimbic brain regions, leading to euphoria that in some can lead to addiction, targets in which this increased dopaminergic tone may be mitigated have been explored. Further, understanding and targeting mechanisms underlying relapse are fundamental to the success of discovering medications that reduce the reinforcing effects of the drug of abuse, decrease the negative reinforcement or withdrawal/negative affect that occurs during abstinence, or both. Atypical inhibitors of the DA transporter and partial agonists/antagonists at DA D receptors are described as two promising targets for future drug development.
非法使用苯丙胺类兴奋剂(如可卡因和冰毒)等药物的现象仍然对健康和社会构成严重挑战。尽管已经做出了大量努力来开发治疗苯丙胺类兴奋剂使用障碍的药物,但都没有证明是有效的,这使得那些有需求的患者群体得不到治疗,也没有回答应该针对哪些作用机制来开发药物治疗的问题。可卡因和冰毒都能迅速增加中脑边缘区域的多巴胺(DA)水平,导致欣快感,而在某些情况下,欣快感可能导致成瘾,因此探索减少这种多巴胺能亢进的靶点是很有必要的。此外,了解和针对复发的机制是发现能够减少滥用药物的强化作用、减少戒断/负面情绪或两者兼有的药物的成功的基础。多巴胺转运体的非典型抑制剂和多巴胺 D 受体的部分激动剂/拮抗剂被描述为未来药物开发的两个有前途的靶点。