| Literature DB >> 32898444 |
Edward T Morgan1, Cene Skubic2, Choon-Myung Lee1, Kaja Blagotinšek Cokan2, Damjana Rozman2.
Abstract
Many hepatic cytochrome P450 enzymes and their associated drug metabolizing activities are down-regulated in disease states, and much of this has been associated with inflammatory cytokines and their signaling pathways. One such pathway is the induction of inducible nitric oxide synthase (NOS2) and generation of nitric oxide (NO) in many tissues and cells including the liver and hepatocytes. Experiments in the 1990s demonstrated that NO could bind to and inhibit P450 enzymes, and suggested that inhibition of NOS could attenuate, and NO generation could mimic, the down-regulation by inflammatory stimuli of not only P450 catalytic activities but also of mRNA expression and protein levels of certain P450 enzymes. This review will summarize and examine the evidence that NO functionally inhibits and down-regulates P450 enzymes in vivo and in vitro, with a particular focus on the mechanisms by which these effects are achieved.Entities:
Keywords: Cytochrome P450; enzyme inhibition; gene transcription; inflammation; nitric oxide; protein degradation
Year: 2020 PMID: 32898444 PMCID: PMC7709541 DOI: 10.1080/03602532.2020.1817061
Source DB: PubMed Journal: Drug Metab Rev ISSN: 0360-2532 Impact factor: 4.518