Impairment of glucagon-induced hepatic system a activity by short-term ethanol administration in the rat

Mark E. Mailliard, Rohit Cariappa, Robert K. Banks

Research output: Contribution to journalArticlepeer-review

5 Scopus citations


Background/Aims: System A is a membrane-bound, hormonally regulated carrier of amino acids that is induced by liver regeneration and impaired by ethanol. The mechanism of ethanol inhibition of system A is unknown; this study examines the effects of ethanol on the subcellular expression of system A activity following hormonal induction. Methods: Following hormonal treatment and short-term ethanol administration to rats, isolated liver Golgi and plasma membrane vesicles were examined for system A transport, and the kinetic parameters were determined. Results: Four hours after ethanol administration, the initial rate of system A activity was depressed 30% ± 9% and 19% ± 7% into Golgi and plasma membrane vesicles, respectively. The affinity constant of 2-(methylamino)-isobutyric acid uptake was unchanged between control and ethanol-treated vesicles, regardless of their subcellular origin. However, the maximal velocity of system A transport decreased from 1030 to 850 pmol ·mg-1 protein ·10 s-1 in Golgi vesicles and from 740 to 355 pmol ·mg-1 protein 10 s-1 in plasma membrane vesicles. Conclusions: Ethanol impairs hormonally induced system A activity in Golgi as well as in the plasma membrane vesicles. Ethanol potentially reduces glucagon induction of system A activity through an impairment of carrier biosynthesis or expression.

Original languageEnglish (US)
Pages (from-to)480-487
Number of pages8
Issue number2
StatePublished - Feb 1994
Externally publishedYes

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology


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