Pyruvate inhibition of pyruvate dehydrogenase kinase. Effects of progressive starvation and hyperthyroidism in vivo, and of dibutyryl cyclic AMP and fatty acids in cultured cardiac myocytes

FEBS Lett. 1996 Sep 16;393(2-3):174-8. doi: 10.1016/0014-5793(96)00877-0.

Abstract

Both prolonged starvation and hyperthyroidism evoke stable increases in cardiac pyruvate dehydrogenase kinase (PDHK) activity. Pyruvate inhibits PDHK in rat heart mitochondria with activation of PDHC. The sensitivity of PDHK to inhibition by pyruvate declines after prolonged starvation. In the present study, pyruvate concentrations giving 50% active complex (PDHa) in mitochondria from fed, control and fed, hyperthyroid rats were 0.3 and 0.8 mM, respectively, compared with 1.0 and 2.8 mM, respectively in mitochondria from 24-h-starved and 48-h-starved rats. The results demonstrate that altered pyruvate sensitivity is not of necessity linked with altered PDHK activity. PDHK activities in mitochondria prepared from cardiac myocytes from fed rats were increased after culture for 24 h with dibutyryl cyclic AMP (50 microM) plus n-octanoate (1 mM), with a concomitant decline in sensitivity of PDHK to pyruvate inhibition, suggesting that changes in sensitivity of PDHK to pyruvate inhibition in vivo may be secondary to increased fatty acid supply and cyclic AMP concentrations.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bucladesine / pharmacology*
  • Caprylates / pharmacology*
  • Cells, Cultured
  • Female
  • Hyperthyroidism / enzymology*
  • Kinetics
  • Mitochondria, Heart / enzymology*
  • Protein Kinase Inhibitors
  • Protein Kinases / metabolism*
  • Protein-Serine-Threonine Kinases
  • Pyruvate Dehydrogenase (Acetyl-Transferring) Kinase
  • Pyruvic Acid / pharmacology*
  • Rats
  • Reference Values
  • Starvation*
  • Triiodothyronine

Substances

  • Caprylates
  • Protein Kinase Inhibitors
  • Pyruvate Dehydrogenase (Acetyl-Transferring) Kinase
  • Triiodothyronine
  • Bucladesine
  • Pyruvic Acid
  • Protein Kinases
  • Protein-Serine-Threonine Kinases
  • octanoic acid