Key result
Diabetic db/db mice exhibited signs of a progressive cardiomyopathy, where increased fatty acid oxidation preceded reductions in carbohydrate oxidation and reduced postischemic recovery of function.
Diabetic db/db mice exhibit a progressive cardiomyopathy characterized by early increases in fatty acid oxidation followed by reduced carbohydrate oxidation and impaired contractile and postischemic function.
Does not support clinical changes; leaves open whether age-dependent metabolic shifts drive human diabetic cardiomyopathy.
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.
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Aasum et al. (2003) studied Diabetes. Diabetic db/db genotype vs. Control (db/+) mice was evaluated on Palmitate and carbohydrate metabolism, contractile function, and postischemic recovery. Diabetic db/db mice exhibited signs of a progressive cardiomyopathy, where increased fatty acid oxidation preceded reductions in carbohydrate oxidation and reduced postischemic recovery of function.
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