Smith Rosemary T, Gruber Staci A
Marijuana Investigations for Neuroscientific Discovery (MIND) Program, McLean Imaging Center, McLean Hospital, Belmont, MA, United States.
Department of Psychiatry, Harvard Medical School, Boston, MA, United States.
Front Psychiatry. 2023 Jan 10;13:1055481. doi: 10.3389/fpsyt.2022.1055481. eCollection 2022.
The majority of states have fully legalized the use of medical cannabis (MC), and nearly all other states allow limited access to cannabidiol (CBD), a non-intoxicating constituent of cannabis often touted for a range of therapeutic indications. Further, the Agricultural Improvement Act of 2018 legalized hemp-derived products in all 50 states; typically high in CBD, these products are derived from cannabis varieties containing ≤0.3% delta-9-tetrahydrocannabinol (THC) by weight. The recent "green rush" has resulted in a striking increase in cannabis use among patients and consumers who often use a wide variety of novel product types, each with a unique blend of cannabinoid constituents. Importantly, however, several cannabinoids have the potential to cause drug-drug interactions (DDI) with other medications, primarily due to their involvement with the hepatic cytochrome P450 (CYP450) system. This article examines the potential for individual cannabinoids, particularly CBD, to interact with the hepatic metabolic system, which is concerning given its involvement in the metabolism of commonly-prescribed medications. CBD and other cannabinoids are metabolized extensively by the CYP450 system, and also inhibit many of these enzymes, potentially leading to variable serum levels of other medications, as well as variable levels of cannabinoids when other medications modify the system. As access and interest in cannabinoid-based products continues to increase, critical questions remain unanswered regarding their safety. The complex relationship between cannabinoids and the hepatic metabolic system, including common potential DDI resulting from cannabinoid exposure, are explored along with the clinical significance of these potential interactions and monitoring or mitigation strategies.
大多数州已全面将医用大麻(MC)的使用合法化,几乎所有其他州都允许有限制地获取大麻二酚(CBD),这是大麻的一种无致幻作用的成分,常因一系列治疗适应症而受到吹捧。此外,2018年的《农业改进法案》使大麻衍生产品在所有50个州合法化;这些产品通常富含CBD,源自按重量计含≤0.3% δ-9-四氢大麻酚(THC)的大麻品种。最近的“绿色热潮”导致患者和消费者中使用大麻的人数显著增加,他们经常使用各种各样的新型产品类型,每种产品都含有独特的大麻素成分组合。然而,重要的是,几种大麻素有可能与其他药物发生药物相互作用(DDI),主要是因为它们与肝脏细胞色素P450(CYP450)系统有关。本文探讨了个别大麻素,特别是CBD,与肝脏代谢系统相互作用的可能性,鉴于其参与常用处方药的代谢,这令人担忧。CBD和其他大麻素被CYP450系统广泛代谢,并且还会抑制许多这些酶,这可能导致其他药物的血清水平变化,以及当其他药物改变该系统时大麻素水平的变化。随着基于大麻素的产品的获取和关注度持续增加,关于其安全性的关键问题仍未得到解答。本文探讨了大麻素与肝脏代谢系统之间的复杂关系,包括大麻素暴露导致的常见潜在DDI,以及这些潜在相互作用的临床意义和监测或缓解策略。