Abstract

BackgroundAlthough clinical diabetes mellitus is obviously a high risk factor for myocardial infarction (MI), in experimental studies disagreement exists about the sensitivity to ischemic injury of an infarcted myocardium. Recently, our group demonstrated that diabetic animals presented better cardiac function recovery and cellular resistance to ischemic injury than nondiabetics. In the present study, we evaluated the chronic effects of MI on left ventricular (LV) and autonomic functions in streptozotocin (STZ) diabetic rats.MethodsMale Wistar rats were divided into 4 groups: control (C, n = 15), diabetes (D, n = 16), MI (I, n = 21), and diabetes + MI (DI, n = 30). MI was induced 15 days after diabetes (STZ) induction. Ninety days after MI, LV and autonomic functions were evaluated (8 animals each group). Left ventricular homogenates were analyzed by Western blotting to evaluate the expression of calcium handling proteins.ResultsMI area was similar in infarcted groups (~43%). Ejection fraction and +dP/dt were reduced in I compared with DI. End-diastolic pressure was additionally increased in I compared with DI. Compared with DI, I had increased Na+-Ca2+ exchange and phospholamban expression (164%) and decreased phosphorylated phospholamban at serine16 (65%) and threonine17 (70%) expression. Nevertheless, diabetic groups had greater autonomic dysfunction, observed by baroreflex sensitivity and pulse interval variability reductions. Consequently, the mortality rate was increased in DI compared with I, D, and C groups.ConclusionsLV dysfunction in diabetic animals was attenuated after 90 days of myocardial infarction and was associated with a better profile of calcium handling proteins. However, this positive adaptation was not able to reduce the mortality rate of DI animals, suggesting that autonomic dysfunction is associated with increased mortality in this group. Therefore, it is possible that the better cardiac function has been transitory, and the autonomic dysfunction, more prominent in diabetic group, may lead, in the future, to the cardiovascular damage.

Highlights

  • Diabetes has been associated with an increased risk of cardiovascular abnormalities and microvascular complications

  • Experimental studies [6,7,8] using an ischemia/reperfusion protocol have shown that hearts from streptozotocin (STZ) diabetic rats that undergo a period of no-flow ischemia have a reduced myocardial infarction (MI) area and recovered ventricular function significantly better than nondiabetic hearts, indicating a possible cardioprotective role of hyperglycemia

  • Left Ventricular Function: Noninvasive and Invasive Evaluations The myocardial infarction akinetic area (MI area) measured by echocardiography was similar between infarcted groups at the initial (I: ± 3 and DI: ± 3% of left ventricular (LV) wall) and final (I: 47 ± 2 and DI: 40 ± 4% of LV wall) evaluations

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Summary

Introduction

Diabetes has been associated with an increased risk of cardiovascular abnormalities and microvascular complications. Clinical studies have demonstrated that diabetes, with consequent cardiomyopathy and cardiovascular neuropathy, is. In this regard, experimental data have demonstrated that hyperglycemia in diabetic animals leads to changes in the heart that contribute to injury during and following an ischemic event; the response of an uncontrolled hyperglycemic diabetic heart to ischemic injury remains controversial [3,4,5]. Experimental studies [6,7,8] using an ischemia/reperfusion protocol have shown that hearts from streptozotocin (STZ) diabetic rats that undergo a period of no-flow ischemia have a reduced myocardial infarction (MI) area and recovered ventricular function significantly better than nondiabetic hearts, indicating a possible cardioprotective role of hyperglycemia. We evaluated the chronic effects of MI on left ventricular (LV) and autonomic functions in streptozotocin (STZ) diabetic rats

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