Inactivation of pyruvate dehydrogenase complex in heart muscle mitochondria of gold-thioglucose-induced obese mice is not due to a stable increase in activity of pyruvate dehydrogenase kinase

Biochem J. 1988 Jul 1;253(1):291-4. doi: 10.1042/bj2530291.

Abstract

The proportion of pyruvate dehydrogenase (PDH) complex in the active dephosphorylated form was decreased (compared with fed lean control mice) in heart muscle mitochondria after the induction of obesity with gold-thioglucose (by 54%) or starvation of lean mice for 48 h (by 81%). The effects of obesity to inactivate PDH complex were demonstrable 4 weeks after administration of gold-thioglucose, and occurred despite significant hyperinsulinaemia in obese animals. Phosphorylation and inactivation of PDH complex in mouse heart muscle in starvation was attributed to a stable increase (2.7-fold) in the activity of PDH kinase as measured in extracts of mitochondria mediated by increased specific activity of a protein activator of PDH kinase (KAP) [Denyer, Kerbey & Randle (1986) Biochem. J. 239, 347-354]. In obese mice no such increase in kinase activity was observed, and we conclude that phosphorylation and inactivation of PDH complex in heart muscle in obesity is not mediated by KAP, but rather is a consequence of increased lipid oxidation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aurothioglucose
  • Blood Glucose / metabolism
  • Body Weight / drug effects
  • Fatty Acids, Nonesterified / blood
  • Insulin / blood
  • Mice
  • Mitochondria, Heart / enzymology*
  • Obesity / blood
  • Obesity / chemically induced
  • Obesity / enzymology*
  • Protein Kinases / metabolism*
  • Protein Serine-Threonine Kinases
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase
  • Pyruvate Dehydrogenase Complex / antagonists & inhibitors*
  • Starvation / enzymology

Substances

  • Blood Glucose
  • Fatty Acids, Nonesterified
  • Insulin
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase
  • Pyruvate Dehydrogenase Complex
  • Aurothioglucose
  • Protein Kinases
  • Protein Serine-Threonine Kinases