Inhibition and induction of CYP enzymes in humans: an update
- PMID: 33111191
- PMCID: PMC7603454
- DOI: 10.1007/s00204-020-02936-7
Inhibition and induction of CYP enzymes in humans: an update
Abstract
The cytochrome P450 (CYP) enzyme family is the most important enzyme system catalyzing the phase 1 metabolism of pharmaceuticals and other xenobiotics such as herbal remedies and toxic compounds in the environment. The inhibition and induction of CYPs are major mechanisms causing pharmacokinetic drug-drug interactions. This review presents a comprehensive update on the inhibitors and inducers of the specific CYP enzymes in humans. The focus is on the more recent human in vitro and in vivo findings since the publication of our previous review on this topic in 2008. In addition to the general presentation of inhibitory drugs and inducers of human CYP enzymes by drugs, herbal remedies, and toxic compounds, an in-depth view on tyrosine-kinase inhibitors and antiretroviral HIV medications as victims and perpetrators of drug-drug interactions is provided as examples of the current trends in the field. Also, a concise overview of the mechanisms of CYP induction is presented to aid the understanding of the induction phenomena.
Keywords: Cytochrome P450; Drug–drug interaction; Environmental toxicants; Herbal remedies; Induction; Inhibition.
Conflict of interest statement
The authors declare that they have no conflict of interest.
Similar articles
-
Cytochrome P450 Structure, Function and Clinical Significance: A Review.Curr Drug Targets. 2018;19(1):38-54. doi: 10.2174/1389450118666170125144557. Curr Drug Targets. 2018. PMID: 28124606 Review.
-
Induction of cytochrome P450 enzymes: a view on human in vivo findings.Expert Rev Clin Pharmacol. 2012 Sep;5(5):569-85. doi: 10.1586/ecp.12.39. Expert Rev Clin Pharmacol. 2012. PMID: 23121279 Review.
-
Inhibition and induction of cytochrome P450 and the clinical implications.Clin Pharmacokinet. 1998 Nov;35(5):361-90. doi: 10.2165/00003088-199835050-00003. Clin Pharmacokinet. 1998. PMID: 9839089 Review.
-
Mechanism-based inactivation of cytochromes P450: implications in drug interactions and pharmacotherapy.Xenobiotica. 2024 Sep;54(9):575-598. doi: 10.1080/00498254.2024.2395557. Epub 2024 Aug 28. Xenobiotica. 2024. PMID: 39175333 Review.
-
Effect of kanglaite on rat cytochrome P450.Pharm Biol. 2015 Jul;53(7):995-1001. doi: 10.3109/13880209.2014.952833. Epub 2014 Dec 4. Pharm Biol. 2015. PMID: 25472767
Cited by
-
Case report: Therapeutic drug monitoring and CYP2D6 phenoconversion in a protracted paroxetine intoxication.Front Pharmacol. 2024 Sep 4;15:1444857. doi: 10.3389/fphar.2024.1444857. eCollection 2024. Front Pharmacol. 2024. PMID: 39295933 Free PMC article.
-
Mitochondria as the Target of Hepatotoxicity and Drug-Induced Liver Injury: Molecular Mechanisms and Detection Methods.Int J Mol Sci. 2022 Mar 18;23(6):3315. doi: 10.3390/ijms23063315. Int J Mol Sci. 2022. PMID: 35328737 Free PMC article. Review.
-
Inhibitory effects of Thai herbal extracts on the cytochrome P450 3A-mediated the metabolism of gefitinib, lapatinib and sorafenib.Toxicol Rep. 2022 Oct 4;9:1846-1852. doi: 10.1016/j.toxrep.2022.10.004. eCollection 2022. Toxicol Rep. 2022. PMID: 36518483 Free PMC article.
-
Effect of polypharmacy on plasma bepridil concentration in patients with heart failure: a multicenter retrospective study.J Pharm Health Care Sci. 2023 Mar 6;9(1):10. doi: 10.1186/s40780-023-00278-x. J Pharm Health Care Sci. 2023. PMID: 36872399 Free PMC article.
-
Design, synthesis and in silico molecular docking evaluation of novel 1,2,3-triazole derivatives as potent antimicrobial agents.Heliyon. 2024 Mar 24;10(7):e27773. doi: 10.1016/j.heliyon.2024.e27773. eCollection 2024 Apr 15. Heliyon. 2024. PMID: 38590856 Free PMC article.
References
-
- Abbas R, Hsyu P. Clinical pharmacokinetics and pharmacodynamics of bosutinib. Clin Pharmacokinet. 2016;55:1191–1204. - PubMed
-
- Abbas R, Leister C, El Gaaloul M, Chalon S, Sonnichsen D. Ascending single-dose study of the safety profile, tolerability, and pharmacokinetics of bosutinib coadministered with ketoconazole to healthy adult subjects. Clin Ther. 2012;34:2011–2019.e1. - PubMed
-
- Abbas R, Boni J, Sonnichsen D. Effect of rifampin on the pharmacokinetics of bosutinib, a dual Src/Abl tyrosine kinase inhibitor, when administered concomitantly to healthy subjects. Drug Metab Pers Ther. 2015;30:57–63. - PubMed
-
- Abel S, Back DJ, Vourvahis M. Maraviroc: pharmacokinetics and drug interactions. Antivir Ther (Lond) 2009;14:607–618. - PubMed
-
- Abraham K, Geusau A, Tosun Y, Helge H, Bauer S, Brockmoller J. Severe 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) intoxication: insights into the measurement of hepatic cytochrome P450 1A2 induction. Clin Pharmacol Ther. 2002;72:163–174. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources