Literature DB >> 30039377

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

Tae Yeon Kong1, Ju-Hyun Kim2, Dong Kyun Kim1, Hye Suk Lee3.   

Abstract

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, ∆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.

Entities:  

Keywords:  Cannabinoids; Cytochrome P450; Drug interaction; Metabolism; UDP-glucuronosyltransferases

Mesh:

Substances:

Year:  2018        PMID: 30039377     DOI: 10.1007/s12272-018-1055-x

Source DB:  PubMed          Journal:  Arch Pharm Res        ISSN: 0253-6269            Impact factor:   4.946


  7 in total

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3.  In Vitro Inhibitory Effects of APINACA on Human Major Cytochrome P450, UDP-Glucuronosyltransferase Enzymes, and Drug Transporters.

Authors:  Sunjoo Kim; Won-Gu Choi; Mihwa Kwon; Sowon Lee; Yong-Yeon Cho; Joo Young Lee; Han Chang Kang; Im-Sook Song; Hye Suk Lee
Journal:  Molecules       Date:  2019-08-19       Impact factor: 4.411

Review 4.  An Update on the Implications of New Psychoactive Substances in Public Health.

Authors:  Ana Y Simão; Mónica Antunes; Emanuel Cabral; Patrik Oliveira; Luana M Rosendo; Ana Teresa Brinca; Estefânia Alves; Hernâni Marques; Tiago Rosado; Luís A Passarinha; Maristela Andraus; Mário Barroso; Eugenia Gallardo
Journal:  Int J Environ Res Public Health       Date:  2022-04-17       Impact factor: 4.614

5.  Cannabis health knowledge and risk perceptions among Canadian youth and young adults.

Authors:  Cesar Leos-Toro; Geoffrey T Fong; Samantha B Meyer; David Hammond
Journal:  Harm Reduct J       Date:  2020-08-03

6.  In Vitro Interaction of AB-FUBINACA with Human Cytochrome P450, UDP-Glucuronosyltransferase Enzymes and Drug Transporters.

Authors:  Sunjoo Kim; Dong Kyun Kim; Yongho Shin; Ji-Hyeon Jeon; Im-Sook Song; Hye Suk Lee
Journal:  Molecules       Date:  2020-10-08       Impact factor: 4.411

7.  Significance of Competing Metabolic Pathways for 5F-APINACA Based on Quantitative Kinetics.

Authors:  Anna O Pinson; Dakota L Pouncey; Mary A Schleiff; William E Fantegrossi; Paul L Prather; Anna Radominska-Pandya; Gunnar Boysen; Grover P Miller
Journal:  Molecules       Date:  2020-10-20       Impact factor: 4.411

  7 in total

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