Abstract
This article is a report on a symposium entitled "Physiological Regulation of Drug Metabolism and Transport" sponsored by the American Society for Pharmacology and Experimental Therapeutics and held at the Experimental Biology 2017 meeting in Chicago, IL. The contributions of physiological and pathophysiological regulation of drug metabolizing enzymes and transporters to interindividual variability in drug metabolism are increasingly recognized, but are in many cases not well understood. The presentations herein discuss the phenomenology, consequences and mechanism of such regulation. CYP2D6 transgenic mice were used to provide insights to the mechanism of regulation of this enzyme in pregnancy, via hepatocyte nuclear factor 4α, small heterodimer partner, and retinoids. Regulation of intestinal and hepatic drug processing enzymes by the intestinal microbiota via tryptophan and its metabolites was investigated. The potential impact of parasitic infections on human drug metabolism and clearance was assessed in mice infected with Schistosoma mansoni or Plasmodium chabaudi chabaudi AS, both of which produced widespread and profound effects on murine hepatic drug metabolizing enzymes. Finally, the induction of Abcc drug efflux transporters by fasting was investigated. This was demonstrated to occur via a cAMP, protein kinase A/Nuclear factor-E2 related factor 2/ Sirtuin 1 pathway via antioxidant response elements on the Abcc genes.
- cytochrome P450
- efflux transporters (P-gp, BCRP, MRP, MATE, BSEP, etc)
- gene regulation/transcription
- microbiome
- Nrf2
- nuclear receptors
- Uptake transporters (OATP, OAT, OCT, PEPT, MCT, NTCP, ASBT, etc.)
- The American Society for Pharmacology and Experimental Therapeutics