Alterations in the regulatory properties of hepatic fatty acid oxidation and carnitine palmitoyltransferase I activity after ethanol feeding and withdrawal

Alcohol Clin Exp Res. 1990 Jun;14(3):472-7. doi: 10.1111/j.1530-0277.1990.tb00506.x.

Abstract

The effects of prolonged ethanol feeding on the regulatory properties of both hepatic fatty acid oxidation and carnitine palmitoyltransferase I activity (CPT-I) were studied in rats fed a high-fat diet containing 36% of total calories as ethanol (ethanol group) or an isocaloric amount of carbohydrate (control group). Prolonged ethanol feeding progressively decreased CPT-I activity and increased enzyme sensitivity and sensitization to inhibition by malonyl-CoA in liver mitochondria. Similarly, long-term ethanol feeding progressively increased the sensitivity of CPT-I, as well as that of fatty acid oxidation, to inhibition by 4-hydroxyphenylglyoxylate. Short-term addition of ethanol or acetaldehyde to the incubations markedly increased the sensitivity of CPT-I to inhibition by malonyl-CoA in a subsequent assay in hepatocytes isolated from ethanol-treated rats, but not in cells from control animals. This effect may be mediated by the ethanol- or acetaldehyde-induced increase of intracellular malonyl-CoA levels. The present results show that ethanol feeding to rats leads to profound alterations in the regulatory properties of hepatic CPT-I, which seem to be determinant for the decreased capacity of fatty acid oxidation by the liver in this state. Nevertheless, all the above-mentioned alterations of the fatty acid oxidative system were reversible, disappearing after 2 to 4 days of ethanol withdrawal.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetaldehyde / metabolism
  • Acyltransferases / metabolism*
  • Alcoholism / enzymology*
  • Animals
  • Carnitine O-Palmitoyltransferase / antagonists & inhibitors
  • Carnitine O-Palmitoyltransferase / metabolism*
  • Ethanol / adverse effects*
  • Fatty Acids / metabolism*
  • Isoenzymes / antagonists & inhibitors
  • Isoenzymes / metabolism*
  • Male
  • Malonyl Coenzyme A / metabolism
  • Mitochondria, Liver / enzymology*
  • Oxidation-Reduction
  • Rats
  • Substance Withdrawal Syndrome / enzymology*

Substances

  • Fatty Acids
  • Isoenzymes
  • Ethanol
  • Malonyl Coenzyme A
  • Acyltransferases
  • Carnitine O-Palmitoyltransferase
  • Acetaldehyde