Preservation of glucose metabolism in hypertrophic GLUT4-null hearts

Am J Physiol Heart Circ Physiol. 2000 Jul;279(1):H313-8. doi: 10.1152/ajpheart.2000.279.1.H313.

Abstract

GLUT4-null mice lacking the insulin-sensitive glucose transporter are not diabetic but do exhibit abnormalities in glucose and lipid metabolism. The most striking morphological consequence of ablating GLUT4 is cardiac hypertrophy. GLUT4-null hearts display characteristics of hypertrophy caused by hypertension. However, GLUT4-null mice have normal blood pressure and maintain a normal cardiac contractile protein profile. Unexpectedly, although they lack the predominant glucose transporter in the heart, GLUT4-null hearts transport glucose and synthesize glycogen at normal levels, but gene expression of rate-limiting enzymes involved in fatty acid oxidation is decreased. The GLUT4-null heart represents a unique model of hypertrophy that may be used to study the consequences of altered substrate utilization in normal and pathophysiological conditions.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Blood Pressure
  • Cardiomegaly / genetics
  • Cardiomegaly / pathology
  • Cardiomegaly / physiopathology*
  • Deoxyglucose / metabolism
  • Diastole
  • Female
  • Glucose / metabolism*
  • Glucose Transporter Type 4
  • Hypertension / genetics
  • Hypertension / pathology
  • Hypertension / physiopathology
  • Magnetic Resonance Imaging
  • Male
  • Mice
  • Mice, Knockout
  • Monosaccharide Transport Proteins / deficiency
  • Monosaccharide Transport Proteins / genetics
  • Monosaccharide Transport Proteins / metabolism*
  • Muscle Proteins*
  • Myocardium / pathology*
  • Sex Characteristics

Substances

  • Glucose Transporter Type 4
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Slc2a4 protein, mouse
  • Deoxyglucose
  • Glucose