Role of hepatic blood flow and metabolism in the pharmacokinetics of ten drugs in lean, aged and obese rats

Xenobiotica. 2014 Dec;44(12):1108-16. doi: 10.3109/00498254.2014.932470. Epub 2014 Jun 20.

Abstract

1. The effect of age and obesity on the pharmacokinetics (PK), hepatic blood flow (HBF) and liver metabolism of 10 compounds was determined in rats. The animals fed a high-fat diet were defined as the diet-induced obese (DIO) group, while the animals that were aged similar to the DIO rats but not fed with high-fat diet were called the age-matched (AM) group. 2. The clearance (CL) values of high CL compounds (CL > 50 mL/min/kg, namely propranolol, diazepam, phenytoin, ethinylestradiol, lorcaserin and fenfluramine) decreased significantly (1.5- to 6-fold) in DIO and AM rats as compared to lean rats, while there was no clear trend for change in CL for the low-to-moderate CL compounds (CL < 50 mL/min/kg, namely atenolol, chlorzoxazone, vancomycin and sibutramine). Hepatocytes incubations revealed a change in half life (t1/2) only for phenytoin. The body weight normalized liver weights and HBF of AM and DIO rats were found to be 2- to 3-fold lower than in lean rats. 3. Our findings suggest that age, and diet to a lesser extent, can reduce HBF and body normalized liver weights and, hence, also reduce CL values for high CL compounds in rats.

Keywords: Altered clearance; CYP2E1; diet-induced obesity; efficacy models; hepatic blood flow; metabolism; pharmacokinetics; urinary clearance.

MeSH terms

  • Aging / physiology*
  • Animals
  • Cells, Cultured
  • Dietary Fats / adverse effects
  • Half-Life
  • Hepatocytes / metabolism
  • Liver / blood supply*
  • Liver / metabolism*
  • Obesity / etiology
  • Obesity / metabolism*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Dietary Fats