Sulfation of Acetaminophen and Acetaminophen-Induced Alterations in Sulfate and 3'-phosphoadenosine 5'-phosphosulfate Homeostasis in Rats With Deficient Dietary Intake of Sulfur

Drug Metab Dispos. Sep-Oct 1994;22(5):725-30.

Abstract

Sulfation of drugs depends on the availability of 3'-phosphoadenosine 5'-phosphosulfate (PAPS), which requires inorganic sulfate for its synthesis. Therefore, decreased alimentary intake of inorganic sulfate or its precursor, cysteine, may compromise sulfation of xenobiotics. To test this hypothesis, separate groups of rats were maintained for 5 days on synthetic diets, which lacked sulfate, or cysteine, or both sulfate and cysteine. These dietary restrictions did not cause growth retardation or depletion of glutathione in liver. Under anesthesia, the animals were injected with acetaminophen (0.5 mmol/kg, i.v.) and elimination of acetaminophen from blood and excretion of acetaminophen metabolites in urine and bile was simultaneously quantified. Deficient intake of inorganic sulfate or cysteine alone did not significantly change elimination and biotransformation of acetaminophen. Combined nutritional deficiency of sulfate and cysteine, however, resulted in a 40% reduction in the excretion of acetaminophen-sulfate, quantitatively the most significant metabolite. Concomitantly, these animals eliminated acetaminophen from blood at a slower rate and converted more acetaminophen to its toxic intermediate, as indicated by increased excretion of acetaminophen-thioether conjugates. Serum and tissue sulfate concentrations were decreased to significantly lower levels in rats on sulfate and cysteine deficient diets, than in rats with a sufficient sulfur supply. Thus, reduced sulfation is apparently caused by diminished availability of inorganic sulfate for PAPS synthesis, even though hepatic and renal PAPS levels were not depleted more by acetaminophen in rats with deficient dietary supply of sulfate and cysteine than in rats with adequate sulfur intake.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetaminophen / pharmacokinetics*
  • Acetaminophen / pharmacology*
  • Acetaminophen / urine
  • Animals
  • Bile / metabolism
  • Biotransformation
  • Cysteine / deficiency
  • Diet
  • Homeostasis / drug effects*
  • Male
  • Phosphoadenosine Phosphosulfate / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Sulfates / metabolism*
  • Sulfur / metabolism*

Substances

  • Sulfates
  • Acetaminophen
  • Phosphoadenosine Phosphosulfate
  • Sulfur
  • Cysteine