This study was designed to study the pathogenesis of cardiomyopathy in anim
als with longstanding (6 months) diabetes mellitus. Male Wistar rats were m
ade diabetic by the injection of streptozotocin (35 mg/kg) intraperitoneal
at 6 months of age, Myocardial contractility was evaluated at 1 year of age
by an echocardiogram. Blood was collected at that time to measure blood gl
ucose and hemoglobin A(1c) as an indicator of metabolic control. Serum carn
itine was also measured on the same sample to evaluate the availability of
this substance so essential for fatty acid metabolism in the myocardium. My
ocardial anatomy was evaluated by both light and electron microscopy after
the animals had diabetes for 6 months. It was found that the left ventricul
ar volume was greater at the end of systole and diastole. There was the sug
gestion of left ventricular fractional shortening and calculated reduced ej
ection fraction indicating decreased contractility consistent with cardiomy
opathy, The hearts had no evidence of coronary vascular occlusion, and the
serum cholesterol was normal. Myocardial ultrastructure revealed abnormal-a
ppearing mitochondria consistent with carnitine deficiency. Serum and myoca
rdial carnitine levels in the animals with diabetes and reduced myocardial
function were low. Carnitine levels and metabolism could be important in th
e pathogenesis of diabetic cardiomyopathy. (C) 1999 Elsevier Science Inc.