Hypercholesterolemia reduces the expression and function of hepatic drug metabolizing enzymes and transporters in rats

Toxicol Lett. 2022 Jul 1:364:1-11. doi: 10.1016/j.toxlet.2022.05.009. Epub 2022 May 30.

Abstract

Hypercholesterolemia, one of the most common lipid metabolic diseases, may cause severe complications and even death. However, the effect of hypercholesterolemia on drug-metabolizing enzymes and transporters remains unclear. In this report, we established a rat model of diet-induced hypercholesterolemia. Quantitative real-time PCR and Western blot analysis were used to study the mRNA and protein expression of drug-metabolizing enzymes and transporters. The functions of these enzymes and transporters were evaluated by the cocktail assay. In hypercholesterolemic rats, the expression of phase I enzymes (CYP1A2, CYP2C11, CYP2E1, CYP3A1/2, CYP4A1 and FMO1/3) and phase II enzymes (UGT1A1/3, PROG, AZTG, SULT1A1, NAT1 and GSTT1) decreased. In addition, the mRNA levels of drug transporter Slco1a1/2, Slco1b2, Slc22a5, Abcc2, Abcb1a and Abcg2 decreased in rats with hypercholesterolemia, while Abcb1b and Abcc3 increased. The decreased expression of hepatic phase I and II enzymes and transporters may be caused by the changes of CAR, FXR, PXR, and Hnf4α levels. In conclusion, diet-induced hypercholesterolemia changes the expression and function of hepatic drug-metabolizing enzymes and transporters in rats, thereby possibly affecting drug metabolism and pharmacokinetics. In clinical hyperlipidemia, patients should strengthen drug monitoring to avoid possible drug exposure mediated risks.

Keywords: Drug-metabolizing enzyme; Hypercholesterolemia; Nuclear receptor; Pharmacokinetics; Transporter.

MeSH terms

  • Animals
  • Cytochrome P-450 CYP2E1 / metabolism
  • Humans
  • Hypercholesterolemia* / genetics
  • Hypercholesterolemia* / metabolism
  • Liver
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Solute Carrier Family 22 Member 5 / metabolism

Substances

  • Membrane Transport Proteins
  • RNA, Messenger
  • SLC22A5 protein, human
  • Solute Carrier Family 22 Member 5
  • Cytochrome P-450 CYP2E1