Cardona-Acosta Astrid M, Meisser Noelle, Vardeleon Nathan I, Steiner Heinz, Bolaños-Guzmán Carlos A
Department of Psychological and Brain Sciences, and Institute for Neuroscience, Texas A&M University, College Station, TX 77843, USA.
Stanson Toshok Center for Brain Function and Repair, Rosalind Franklin University of Medicine and Science, North Chicago, IL 60064, USA; Discipline of Cellular and Molecular Pharmacology, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL 60064, USA.
Prog Neuropsychopharmacol Biol Psychiatry. 2025 Jan 10;136:111137. doi: 10.1016/j.pnpbp.2024.111137. Epub 2024 Sep 10.
Benzodiazepines are effective in managing anxiety and related disorders when used properly (short-term). Their inappropriate use, however, carries significant risks, involving amnesia, rebound insomnia, rebound anxiety, depression, dependence, abuse, addiction, and an intense and exceedingly prolonged withdrawal, among other complications. Benzodiazepines also amplify the effects of opioids and, consequently, have been implicated in approximately 30 % of opioid overdose deaths. Despite their unfavorable profile, sharp increases in medical and non-medical use of benzodiazepines have been steadily reported worldwide. Alprazolam (Xanax®), a potent, short-acting benzodiazepine, is among the most prescribed and abused anxiolytics in the United States. This medication is commonly co-abused with opioids, increasing the likelihood for oversedation, overdose, and death. Notwithstanding these risks, it is surprising that research investigating how benzodiazepines, such as alprazolam, interact with opioids is severely lacking in clinical and preclinical settings. This review therefore aims to present our current knowledge of benzodiazepine use and misuse, with an emphasis on alprazolam when data is available, and particularly in populations at higher risk for developing substance use disorders. Additionally, the potential mechanism(s) surrounding tolerance, dependence and abuse liability are discussed. Despite their popularity, our understanding of how benzodiazepines and opioids interact is less than adequate. Therefore, it is now more important than ever to understand the short- and long-term consequences of benzodiazepine/alprazolam use.
苯二氮䓬类药物在正确(短期)使用时对管理焦虑及相关障碍有效。然而,其不当使用会带来重大风险,包括失忆、反弹性失眠、反弹性焦虑、抑郁、依赖、滥用、成瘾以及强烈且极其漫长的戒断反应等其他并发症。苯二氮䓬类药物还会增强阿片类药物的作用,因此约30%的阿片类药物过量死亡案例与之有关。尽管存在这些不良情况,但全球范围内苯二氮䓬类药物的医疗和非医疗使用量仍在持续急剧增加。阿普唑仑(佳静安定®)是一种强效短效苯二氮䓬类药物,是美国处方量和滥用率最高的抗焦虑药之一。这种药物常与阿片类药物共同滥用,增加了过度镇静、过量用药和死亡的可能性。尽管存在这些风险,但令人惊讶的是,在临床和临床前环境中,关于阿普唑仑等苯二氮䓬类药物如何与阿片类药物相互作用的研究严重不足。因此,本综述旨在介绍我们目前对苯二氮䓬类药物使用和滥用的认识,在有数据时重点关注阿普唑仑,特别是在有更高物质使用障碍风险的人群中。此外,还讨论了耐受性、依赖性和滥用倾向的潜在机制。尽管它们很受欢迎,但我们对苯二氮䓬类药物和阿片类药物如何相互作用的了解仍不够充分。因此,了解苯二氮䓬类药物/阿普唑仑使用的短期和长期后果现在比以往任何时候都更加重要。