Physiological Regulation of Drug Metabolism and Transport: Pregnancy, Microbiome, Inflammation, Infection, and Fasting

Drug Metab Dispos. 2018 May;46(5):503-513. doi: 10.1124/dmd.117.079905. Epub 2018 Mar 7.

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 physiologic and pathophysiological regulation of drug-metabolizing enzymes and transporters to interindividual variability in drug metabolism are increasingly recognized but in many cases are not well understood. The presentations herein discuss the phenomenology, consequences, and mechanism of such regulation. CYP2D6 transgenic mice were used to provide insights into 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.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antioxidant Response Elements / physiology
  • Biological Transport / physiology*
  • Cytochrome P-450 CYP2D6 / metabolism
  • Fasting / metabolism
  • Fasting / physiology*
  • Female
  • Gastrointestinal Microbiome / physiology
  • Hepatocyte Nuclear Factor 4 / metabolism
  • Humans
  • Inactivation, Metabolic / physiology*
  • Inflammation / metabolism
  • Inflammation / physiopathology*
  • Liver / metabolism
  • Malaria / metabolism
  • Malaria / physiopathology
  • Male
  • Membrane Transport Proteins / metabolism
  • Metabolic Clearance Rate / physiology
  • Mice
  • Mice, Transgenic
  • Microbiota / physiology*
  • Plasmodium chabaudi / pathogenicity
  • Pregnancy
  • Schistosomiasis mansoni / metabolism
  • Schistosomiasis mansoni / physiopathology
  • Tryptophan / metabolism

Substances

  • Hepatocyte Nuclear Factor 4
  • Membrane Transport Proteins
  • Tryptophan
  • Cytochrome P-450 CYP2D6