Cannabinoids and drug metabolizing enzymes: potential for drug-drug interactions and implications for drug safety and efficacy

被引:22
作者
Bardhi, Keti [1 ]
Coates, Shelby [1 ]
Watson, Christy J. W. [1 ]
Lazarus, Philip [1 ,2 ]
机构
[1] Washington State Univ, Coll Pharm & Pharmaceut Sci, Dept Pharmaceut Sci, Spokane, WA 99202 USA
[2] Washington State Univ, Coll Pharm & Pharmaceut Sci, Dept Pharmaceut Sci, 412 E Spokane Falls Blvd, Spokane, WA 99202 USA
关键词
Cannabis; cannabinoids; THC; CBD; cytochrome P450; UDP glucuronosyltransferase; drug-drug interactions; pharmacokinetics; RANDOMIZED-CONTROLLED-TRIAL; UDP-GLUCURONOSYLTRANSFERASES; IN-VITRO; CB2; RECEPTOR; DELTA(9)-TETRAHYDROCANNABINOL THC; PHARMACOKINETIC INTERACTIONS; MAJOR PHYTOCANNABINOIDS; PLASMA PHARMACOKINETICS; HUMAN CARBOXYLESTERASES; PLANT CANNABINOIDS;
D O I
10.1080/17512433.2022.2148655
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionCannabis is an increasingly popular recreational and medicinal drug in the USA. While cannabis is still a Schedule 1 drug federally, many states have lifted the ban on its use. With its increased usage, there is an increased possibility for potential drug-drug interactions (DDI) that may occur with concomitant use of cannabis and pharmaceuticals.Area coveredThis review focuses on the current knowledge of cannabis induced DDI, with a focus on pharmacokinetic DDI arising from enzyme inhibition or induction. Phase I and phase II drug metabolizing enzymes, specifically cytochrome P450s, carboxylesterases, and uridine-5'-diphosphoglucuronosyltransferases, have historically been the focus of research in this field, with much of the current knowledge of the potential for cannabis to induce DDI within these families of enzymes coming from in vitro enzyme inhibition studies. Together with a limited number of in vivo clinical studies and in silico investigations, current research suggests that cannabis exhibits the potential to induce DDI under certain circumstances.Expert opinionBased upon the current literature, there is a strong potential for cannabis-induced DDI among major drug-metabolizing enzymes.
引用
收藏
页码:1443 / 1460
页数:18
相关论文
共 203 条
[11]   Predicting the Potential for Cannabinoids to Precipitate Pharmacokinetic Drug Interactions via Reversible Inhibition or Inactivation of Major Cytochromes P450 [J].
Bansal, Sumit ;
Maharao, Neha ;
Paine, Mary F. ;
Unadkat, Jashvant D. .
DRUG METABOLISM AND DISPOSITION, 2020, 48 (10) :1008-1017
[12]   Characterization of Differential Tissue Abundance of Major Non-CYP Enzymes in Human [J].
Basit, Abdul ;
Neradugomma, Naveen K. ;
Wolford, Christopher ;
Fan, Peter W. ;
Murray, Bernard ;
Takahashi, Ryan H. ;
Khojasteh, S. Cyrus ;
Smith, Bill J. ;
Heyward, Scott ;
Totah, Rheem A. ;
Kelly, Edward J. ;
Prasad, Bhagwat .
MOLECULAR PHARMACEUTICS, 2020, 17 (11) :4114-4124
[13]   (-)-Delta(9)-Tetrahydrocannabinol antagonizes the peripheral cannabinoid receptor-mediated inhibition of adenylyl cyclase [J].
Bayewitch, M ;
Rhee, RH ;
AvidorReiss, T ;
Breuer, A ;
Mechoulam, R ;
Vogel, Z .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (17) :9902-9905
[14]   Cytochrome P450-Catalyzed Metabolism of Cannabidiol to the Active Metabolite 7-Hydroxy-Cannabidiol [J].
Beers, Jessica L. ;
Fu, Dong ;
Jackson, Klarissa D. .
DRUG METABOLISM AND DISPOSITION, 2021, 49 (10) :882-891
[15]   Cannabidiol Reduces the Anxiety Induced by Simulated Public Speaking in Treatment-Naive Social Phobia Patients [J].
Bergamaschi, Mateus M. ;
Costa Queiroz, Regina Helena ;
Nisihara Chagas, Marcos Hortes ;
Gomes de Oliveira, Danielle Chaves ;
De Martinis, Bruno Spinosa ;
Kapczinski, Flavio ;
Quevedo, Joao ;
Roesler, Rafael ;
Schroeder, Nadja ;
Nardi, Antonio E. ;
Martin-Santos, Rocio ;
Cecilio Hallak, Jaime Eduardo ;
Zuardi, Antonio Waldo ;
Crippa, Jose Alexandre S. .
NEUROPSYCHOPHARMACOLOGY, 2011, 36 (06) :1219-1226
[16]   CYP2C-catalyzed delta(9)-tetrahydrocannabinol metabolism: Kinetics, pharmacogenetics and interaction with phenytoin [J].
Bland, TM ;
Haining, RL ;
Tracy, TS ;
Callery, PS .
BIOCHEMICAL PHARMACOLOGY, 2005, 70 (07) :1096-1103
[17]   Clinical and Preclinical Evidence for Functional Interactions of Cannabidiol and Δ9-Tetrahydrocannabinol [J].
Boggs, Douglas L. ;
Nguyen, Jacques D. ;
Morgenson, Daralyn ;
Taffe, Michael A. ;
Ranganathan, Mohini .
NEUROPSYCHOPHARMACOLOGY, 2018, 43 (01) :142-154
[18]   Clinical issues in cannabis use [J].
Bonomo, Yvonne ;
Souza, Jose Diogo S. ;
Jackson, Aidan ;
Crippa, Jose Alexandre S. ;
Solowij, Nadia .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2018, 84 (11) :2495-2498
[19]  
Bridgeman Mary Barna, 2017, P T, V42, P180
[20]   Δ-9-tetrahydrocannabinol dose increase leads to warfarin drug interaction and elevated INR [J].
Brown, Geoffrey W. ;
Bellnier, Terrance J. ;
Janda, Maria ;
Miskowitz, Kyle .
JOURNAL OF THE AMERICAN PHARMACISTS ASSOCIATION, 2021, 61 (01) :E57-E60