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Synthetic cannabinoids are substrates and inhibitors of multiple drug-metabolizing enzymes

机译:合成大麻素是多种药物代谢酶的基质和抑制剂

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摘要

Synthetic cannabinoids, a new class of psychoactive substances, are potent agonists of cannabinoid receptors, which mimic the psychoactive effects of the principal psychoactive component of cannabis, a dagger 9-tetrahydrocannabinol. Despite governmental scheduling as illicit drugs, new synthetic cannabinoids are being produced. The abuse of synthetic cannabinoids with several drugs containing different chemical groups has resulted in large numbers of poisonings. This has increased the urgency for forensic and public health laboratories to identify the metabolites of synthetic cannabinoids and apply this knowledge to the development of analytical methods and for toxicity prediction. It is necessary to determine whether synthetic cannabinoids are involved in drug-metabolizing enzyme-mediated drug-drug interactions. This review describes the metabolic pathways of 13 prevalent synthetic cannabinoids and various drug-metabolizing enzymes responsible for their metabolism, including cytochrome P450 (CYP), UDP-glucuronosyltransferases (UGTs), and carboxylesterases. The inhibitory effects of synthetic cannabinoids on CYP and UGT activities are also reviewed to predict the potential of synthetic cannabinoids for drug-drug interactions. The drug-metabolizing enzymes responsible for metabolism of synthetic cannabinoids should be characterized and the effects of synthetic cannabinoids on CYP and UGT activities should be determined to predict the pharmacokinetics of synthetic cannabinoids and synthetic cannabinoid-induced drug-drug interactions in the clinic.
机译:合成大麻素,一种新的精神活性物质,是大麻素受体的有效激动剂,其模仿大麻的主要精神活性成分的精神活性作用,匕首9-四氢甘油醛醇。尽管政府安排为非法药物,正在制作新的合成大麻素。用几种含有不同化学基团的药物滥用合成大麻素,导致大量的中毒。这增加了法医和公共卫生实验室的紧迫性,以确定合成大麻素的代谢产物,并将这些知识应用于分析方法和毒性预测的发展。有必要确定合成大麻素是否参与药物代谢酶介导的药物 - 药物相互作用。该综述描述了13种普遍的合成大麻素和各种药物代谢酶的代谢途径,其代谢包括细胞色素P450(CYP),UDP-葡糖糖核糖基转移酶(UGT)和羧基酯酶。还审查了合成大麻素对CYP和UGT活性的抑制作用,以预测用于药物 - 药物相互作用的合成大麻素的潜力。应表征应表征对合成大麻素代谢负责的药物代谢酶,并应确定合成大麻素对CYP和UGT活性的影响,以预测临床中的合成大麻素和合成大麻素诱导的药物 - 药物相互作用的药代动力学。

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