Key result
Diabetes significantly altered intracellular calcium homeostasis in cardiac endothelial cells by decreasing SERCA and NCX activities, resulting in prolonged calcium decay time and reduced peak amplitude.
Diabetes impairs intracellular calcium homeostasis in cardiac endothelial cells by altering SERCA and NCX activities, providing insight into the pathogenesis of diabetic cardiomyopathy.
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Does not support clinical practice changes; leaves open endothelial calcium dysregulation as a mechanism in human diabetic cardiomyopathy.
Diabetic cardiomyopathy (DCM) is a diabetic complication, which results in myocardial dysfunction independent of other etiological factors. Abnormal intracellular calcium ([Ca(2+)](i)) homeostasis has been implicated in DCM and may precede clinical manifestation. Studies in cardiomyocytes have shown that diabetes results in impaired [Ca(2+)](i) homeostasis due to altered sarcoplasmic reticulum Ca(2+) ATPase (SERCA) and sodium-calcium exchanger (NCX) activity. Importantly, altered calcium homeostasis may also be involved in diabetes-associated endothelial dysfunction, including impaired endothelium-dependent relaxation and a diminished capacity to generate nitric oxide (NO), elevated cell adhesion molecules, and decreased angiogenic growth factors. However, the effect of diabetes on Ca(2+) regulatory mechanisms in cardiac endothelial cells (CECs) remains unknown. The objective of this study was to determine the effect of diabetes on [Ca(2+)](i) homeostasis in CECs in the rat model (streptozotocin-induced) of DCM. DCM-associated cardiac fibrosis was confirmed using picrosirius red staining of the myocardium. CECs isolated from the myocardium of diabetic and wild-type rats were loaded with Fura-2, and UTP-evoked [Ca(2+)](i) transients were compared under various combinations of SERCA, sarcoplasmic reticulum Ca(2+) ATPase (PMCA) and NCX inhibitors. Diabetes resulted in significant alterations in SERCA and NCX activities in CECs during [Ca(2+)](i) sequestration and efflux, respectively, while no difference in PMCA activity between diabetic and wild-type cells was observed. These results improve our understanding of how diabetes affects calcium regulation in CECs, and may contribute to the development of new therapies for DCM treatment.
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Sheikh et al. (2012) studied Diabetic cardiomyopathy. Streptozotocin-induced diabetes vs. Wild-type controls was evaluated on UTP-evoked [Ca2+]i transient decay time and peak amplitude (p=<0.05). Diabetes significantly altered intracellular calcium homeostasis in cardiac endothelial cells by decreasing SERCA and NCX activities, resulting in prolonged calcium decay time and reduced peak amplitude.
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