Plasma membrane vesicles from isolated hepatocytes retain the increase of amino acid transport induced by dibutyryl cyclic AMP in intact cells

Biochim Biophys Acta. 1982 Apr 23;687(1):35-41. doi: 10.1016/0005-2736(82)90167-5.

Abstract

We have investigated the effect of cyclic AMP on hepatic amino acid transport by measuring the uptake of L-alanine in plasma membrane vesicles purified from hepatocytes incubated without or with dibutyryl cyclic AMP. The application of an Na+ gradient to vesicles from hepatocytes exposed to dibutyryl cyclic AMP, compared to control, resulted in a greater transient accumulation of L-alanine, whereas in the presence of a K+ gradient a similar slow equilibration of L-alanine was observed. Kinetic analysis of L-alanine influx revealed that the increased uptake resulted from an increased capacity (Vmax) with no change in the affinity (Km) of the carriers for L-alanine. These results strongly suggest that dibutyryl cyclic AMP induces stable changes at the membrane level probably by increasing the number of amino acid carrier molecules.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine / metabolism*
  • Animals
  • Biological Transport / drug effects
  • Bucladesine / pharmacology*
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Glucagon / metabolism
  • In Vitro Techniques
  • Kinetics
  • Liver / metabolism*
  • Male
  • Rats
  • Rats, Inbred Strains
  • Receptor, Insulin / metabolism
  • Receptors, Cell Surface / metabolism
  • Receptors, Glucagon

Substances

  • Receptors, Cell Surface
  • Receptors, Glucagon
  • Bucladesine
  • Glucagon
  • Receptor, Insulin
  • Alanine