Key result
In isolated heart preparations perfused with glucose alone, aortic output was significantly reduced in obese rats compared to controls (32.6 vs 46.2 ml/min, P < .05), but normalized with fatty acids.
Absolute Event Rate: 32.6% vs 46.2%
p-value: p=< .05
In a rat model of obesity and insulin resistance, elevated circulating fatty acids are crucial for maintaining normal myocardial systolic function.
Should not alter substrate management in obese patients; leaves open fatty acid dependence for systolic function in insulin resistance.
BACKGROUND: Clinical data advocating an adverse effect of obesity on left ventricular (LV) systolic function independent of comorbidities is controversial. We hypothesized that in obesity with prediabetic insulin resistance, circulating fatty acids (FAs) become a valuable fuel source in the maintenance of normal systolic function. METHODS: Male Wistar rats were fed a high caloric diet for 32 weeks to induce obesity. Myocardial LV systolic function was assessed using echocardiography and isolated heart preparations. RESULTS: Aortic output was reduced in obese rat hearts over a range of filling pressures (for example: 15 cmH2O, obese: 32.6 ± 1.2 ml/min vs control: 46.2 ± 0.9 ml/min, P < .05) when perfused with glucose alone. Similarly, the slope of the LV end-systolic pressure-volume relationship decreased, and there was a right shift in the LV end-systolic stress-strain relationship as determined in Langendorff perfused, isovolumic rat heart preparations in the presence of isoproterenol (10(-8)M) (LV systolic stress-strain relationship and a reduced load-independent intrinsic systolic myocardial function, obese: 791 ± 62 g/cm(2) vs control: 1186 ± 74 g/cm(2), P < .01). The addition of insulin to the perfusion buffer improved aortic output, whereas the addition of FAs completely normalized aortic output. LV function was maintained in obese animals in vivo during an inotropic challenge. CONCLUSIONS: Elevated circulating FA levels may be important to maintain myocardial systolic function in the initial stages of obesity and insulin resistance.
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Smith et al. (2016) studied Obesity with prediabetic insulin resistance. High caloric diet to induce obesity vs. Control was evaluated on Aortic output at 15 cmH2O filling pressure when perfused with glucose alone (p=< .05). In isolated heart preparations perfused with glucose alone, aortic output was significantly reduced in obese rats compared to controls (32.6 vs 46.2 ml/min, P < .05), but normalized with fatty acids.
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