Raymond Joel S, Athanasopoulos Alexander G, Badolato Connie J, Doolan Tylah J, Scicluna Rhianne L, Everett Nicholas A, Bowen Michael T, James Morgan H
Department of Psychiatry, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA; Rutgers Addiction Research Center, Brain Health Institute, Rutgers Health, Piscataway, NJ, USA.
School of Psychology, Faculty of Science, University of Sydney, Sydney, NSW, Australia; Brain and Mind Centre, The University of Sydney, Sydney, NSW, Australia.
Pharmacol Biochem Behav. 2025 Mar;248:173952. doi: 10.1016/j.pbb.2024.173952. Epub 2024 Dec 22.
Medications to treat substance use disorders (SUDs) remain suboptimal or, in the case of stimulants and cannabis, non-existent. Many factors have contributed to this paucity, including the biological complexity of addiction, regulatory challenges, and a historical lack of enthusiasm among pharmaceutical companies to commit resources to this disease space. Despite these headwinds, the recent opioid crisis has highlighted the devastating consequences of SUDs for both individuals and society, stimulating urgent efforts to identify novel treatment approaches. In addition, several neurobiological systems have been recently implicated in unique aspects of drug reward, opening the door to candidate medications with novel mechanisms of action. Here, we provide an overview of efforts to target several of these new systems, with a focus on those that are the subject of ongoing clinical trials as well as being areas of interest among the authors' research groups (MHJ, MTB, NAE). Specifically, we discuss new classes of medications targeting the serotonin 2A receptor (i.e., psychedelics), glucagon-like peptide 1 receptor, cannabidiol, dynorphin/kappa opioid receptor, orexin/hypocretin, and oxytocin receptor systems, as well as emergent approaches for modulating the more canonical dopaminergic system via agonist therapies for stimulant use disorders. Collectively, innovations in this space give reason for optimism for an improved therapeutic landscape for substance use disorders in the near future.
用于治疗物质使用障碍(SUDs)的药物仍然不尽人意,或者在兴奋剂和大麻的情况下,根本不存在。造成这种匮乏的因素有很多,包括成瘾的生物学复杂性、监管挑战,以及制药公司历史上缺乏投入资源研究这一疾病领域的热情。尽管存在这些阻碍,但最近的阿片类药物危机凸显了物质使用障碍对个人和社会造成的毁灭性后果,促使人们迫切努力寻找新的治疗方法。此外,最近有几个神经生物学系统被认为与药物奖赏的独特方面有关,为具有新作用机制的候选药物打开了大门。在这里,我们概述了针对其中几个新系统所做的努力,重点关注那些正在进行临床试验的系统以及作者研究团队(MHJ、MTB、NAE)感兴趣的领域。具体而言,我们讨论了针对5-羟色胺2A受体(即致幻剂)、胰高血糖素样肽1受体、大麻二酚、强啡肽/κ阿片受体、食欲素/下丘脑分泌素和催产素受体系统的新型药物类别,以及通过兴奋剂使用障碍激动剂疗法调节更典型多巴胺能系统的新方法。总体而言,这一领域的创新让人们有理由对在不久的将来改善物质使用障碍的治疗前景感到乐观。