Chronic EtOH administration alters liver Mg2+ homeostasis

Am J Physiol Gastrointest Liver Physiol. 2003 Jan;284(1):G57-67. doi: 10.1152/ajpgi.00153.2002.

Abstract

Ethanol (EtOH) administration to rats for 4 wk markedly decreased Mg(2+) content in several tissues, including liver. Total cellular Mg(2+) accounted for 26.8 +/- 2.4 vs. 36.0 +/- 1.4 nmol Mg(2+)/mg protein in hepatocytes from EtOH-fed and control rats, respectively, and paralleled a 13% decrease in cellular ATP content. Stimulation of alpha(1)- or beta-adrenergic receptor or acute EtOH administration did not elicit an extrusion of Mg(2+) from liver cells of EtOH-fed rats while releasing 5% of total tissue Mg(2+) content from hepatocytes of control rats. Despite the 25% decrease in Mg(2+) content, hepatocytes from EtOH-fed rats did not accumulate Mg(2+) following stimulation of protein kinase C signaling pathway, whereas control hepatocytes accumulated approximately 2 nmol Mg(2+). mg protein(-1). 4 min(-1). Together, these data indicate that Mg(2+) homeostasis and transport are markedly impaired in liver cells after prolonged exposure to alcohol. The inability of liver cells, and possibly other tissues, to accumulate Mg(2+) can help explain the reduction in tissue Mg(2+) content following chronic alcohol consumption.

Publication types

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

MeSH terms

  • Adrenergic Agonists / pharmacology
  • Animals
  • Cell Membrane / metabolism
  • Central Nervous System Depressants / pharmacology*
  • Ethanol / pharmacology*
  • Hepatocytes / metabolism
  • Homeostasis / drug effects
  • Liver / cytology
  • Liver / drug effects
  • Liver / metabolism*
  • Magnesium / metabolism*
  • Male
  • Protein Kinase C / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects
  • Signal Transduction / physiology

Substances

  • Adrenergic Agonists
  • Central Nervous System Depressants
  • Ethanol
  • Protein Kinase C
  • Magnesium