Key result
Fasting in rats reduced myocardial injury and improved contractile function during postischemic reperfusion compared to the fed state.
Why the study?
Does fasting alter substrate metabolism and improve contractile function in postischemic rat myocardium?
Does fasting alter substrate metabolism and improve contractile function in postischemic rat myocardium?
In a rat model, fasting alters myocardial substrate selection independently of substrate availability and improves contractile function during postischemic reperfusion, suggesting reduced myocardial injury.
The pattern of substrate utilization may influence postischemic myocardial injury. To characterize the effect of nutritional state on substrate selection and contractile function during control conditions and postischemic reperfusion, hearts from fed and fasted rats were perfused retrogradely with 0.4 mM palmitate, 8 mM glucose, and 175 mU/l insulin. Under control conditions, hearts from fasted rats exhibited lower glucose oxidation (-59%) and higher palmitate oxidation (+191%) than hearts from fed rats. During reperfusion, postischemic hearts exhibited stimulation of glucose-oxidation, with no difference between hearts from fasted and fed rats. However, oxidation of palmitate remained higher after fasting (+68%). Hearts from fasted rats exhibited lower left ventricular diastolic pressure and higher left ventricular systolic pressure development during reperfusion. The results indicate that 1) substrate selection in myocardium is influenced by the nutritional state independently of substrate availability, 2) during postischemic reperfusion, inhibition of glucose oxidation is removed in hearts from fasted rats, whereas inhibition of fatty acid oxidation in hearts from fed rats is maintained, and 3) myocardial injury is lower after fasting.
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Montessuit et al. (1996) studied postischemic myocardial injury. Fasting vs. Fed state was evaluated on substrate selection and contractile function. Fasting in rats reduced myocardial injury and improved contractile function during postischemic reperfusion compared to the fed state.
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