Age-dependent changes in metabolism, contractile function, and ischemic sensitivity in hearts from db/db mice

Diabetes. 2003 Feb;52(2):434-41. doi: 10.2337/diabetes.52.2.434.

Abstract

Glucose and palmitate metabolism and contractile function were measured with ex vivo perfused working hearts from control (db/+) and diabetic (db/db) female mice at 6, 10-12, and 16-18 weeks of age. Palmitate oxidation was increased by 2.2-fold in 6-week-old db/db hearts and remained elevated in 10- to 12- and 16- to 18-week-old hearts. Carbohydrate oxidation was normal at 6 weeks but was reduced to 27 and 23% of control at 10-12 and 16-18 weeks, respectively. At 6 weeks, db/db hearts exhibited a slight reduction in mechanical function, whereas marked signs of dysfunction were evident at 10-12 and 16-18 weeks. Mechanical function after ischemia-reperfusion was examined in hearts from male mice; at 6 weeks, db/db hearts showed normal recovery, whereas at 12 weeks it was markedly reduced. Fatty acid oxidation was the predominant substrate used after reperfusion. Thus, diabetic db/db hearts exhibit signs of a progressive cardiomyopathy; increased fatty acid oxidation preceded reductions in carbohydrate oxidation. Postischemic recovery of function was reduced in db/db hearts, in parallel with age-dependent changes in normoxic contractile performance. Finally, peroxisome proliferator-activated receptor-alpha treatment (3 weeks) did not affect sensitivity to ischemia-reperfusion, even though carbohydrate oxidation was increased and palmitate oxidation was decreased.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging
  • Animals
  • Blood Glucose / metabolism
  • Body Weight
  • Carbohydrate Metabolism
  • Diabetes Mellitus, Type 2 / genetics
  • Diabetes Mellitus, Type 2 / metabolism
  • Diabetes Mellitus, Type 2 / physiopathology*
  • Fatty Acids, Nonesterified / blood
  • Female
  • Heart / growth & development*
  • Heart / physiology*
  • Hemodynamics / physiology*
  • In Vitro Techniques
  • Insulin / blood
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • Myocardial Contraction / physiology*
  • Myocardial Ischemia / genetics
  • Myocardial Ischemia / physiopathology*
  • Myocardium / metabolism*
  • Organ Size
  • Oxidation-Reduction

Substances

  • Blood Glucose
  • Fatty Acids, Nonesterified
  • Insulin