Food restriction stimulates conjugation of p-nitrophenol in perfused rat liver

Arch Biochem Biophys. 1995 Jun 1;319(2):451-6. doi: 10.1006/abbi.1995.1316.

Abstract

Rates of conjugation of p-nitrophenol were studied in livers from normal and food-restricted rats perfused with either p-nitroanisole or p-nitrophenol. Female Sprague-Dawley rats had ad libitum access to a Purina 5001 nonpurified diet (control) or were given 65% of the intake of controls for 3 weeks. Livers were perfused with oxygenated Krebs-Henseleit buffer using a nonrecirculating system. Maximal rates of conjugation of p-nitrophenol, generated either from the O-demethylation of p-nitroanisole (200 microM) or from the infusion of p-nitrophenol (70 microM), were elevated significantly nearly twofold by food restriction. Thus, food restriction stimulates conjugation in the intact liver cell. Specifically, rates of conjugation were increased from 2.1 +/- 0.2 to 3.7 +/- 0.4 and from 3.3 +/- 0.6 to 5.8 +/- 0.5 mumol/g/h when 200 microM p-nitroanisole or 70 microM p-nitrophenol were infused, respectively. On the other hand, rates of conjugation were not affected by food restriction when low concentrations of p-nitroanisole (50 microM) or p-nitrophenol (20 microM) were infused. Further, food restriction did not alter rates of conjugation in isolated microsomes supplemented with excess UDPGA. Interestingly, both UDP-glucose and UDP-glucuronic acid were increased significantly in liver extracts from food-restricted rats when livers were perfused with high but not low concentrations of p-nitrophenol. Under these conditions, the increase in UDP-glucuronic acid was threefold. Moreover, food restriction increased carbohydrate release from the liver about twofold. Glycogen content was also increased significantly in liver extracts from 8.4 +/- 1.9 to 60.4 +/- 13.8 mmol/kg wet weight by food restriction. Taken together, these data support the hypothesis that food restriction stimulates conjugation of p-nitrophenol concentrations by increasing the supply of the pivotal cofactor UDP-glucuronic acid from carbohydrate reserves (e.g., glycogen).

MeSH terms

  • Animals
  • Carbohydrates / analysis
  • Female
  • Food Deprivation / physiology*
  • Glucuronosyltransferase / analysis
  • In Vitro Techniques
  • Liver / metabolism*
  • Microsomes, Liver / metabolism
  • Nitrophenols / metabolism*
  • Perfusion
  • Rats
  • Rats, Sprague-Dawley
  • Uridine Diphosphate Glucuronic Acid / pharmacology

Substances

  • Carbohydrates
  • Nitrophenols
  • Uridine Diphosphate Glucuronic Acid
  • Glucuronosyltransferase
  • 4-nitrophenol