SIRT1 suppresses cardiomyocyte apoptosis in diabetic cardiomyopathy: an insight into endoplasmic reticulum stress response mechanism
R Guo, W Liu, B Liu, B Zhang, W Li, Y Xu - International Journal of …, 2015 - Elsevier
R Guo, W Liu, B Liu, B Zhang, W Li, Y Xu
International Journal of Cardiology, 2015•ElsevierBackground Endoplasmic reticulum (ER) stress-dependent apoptosis had been shown to
occur in the hearts of people with diabetes, although the exact mechanisms are unclear.
Sirtuin 1 (SIRT1), a nicotinamide adenine dinucleotide NAD (+)-dependent deacetylase, is
known to play a role in diabetes-related complications as well as ER-stress. Therefore, we
investigated the relationship between Sirtuin 1 (SIRT1) and ER stress-induced apoptosis in
H9C2 cardiomyocyte. Methods Diabetic rats were established by a single intraperitoneal …
occur in the hearts of people with diabetes, although the exact mechanisms are unclear.
Sirtuin 1 (SIRT1), a nicotinamide adenine dinucleotide NAD (+)-dependent deacetylase, is
known to play a role in diabetes-related complications as well as ER-stress. Therefore, we
investigated the relationship between Sirtuin 1 (SIRT1) and ER stress-induced apoptosis in
H9C2 cardiomyocyte. Methods Diabetic rats were established by a single intraperitoneal …
Background
Endoplasmic reticulum (ER) stress-dependent apoptosis had been shown to occur in the hearts of people with diabetes, although the exact mechanisms are unclear. Sirtuin 1 (SIRT1), a nicotinamide adenine dinucleotide NAD(+)-dependent deacetylase, is known to play a role in diabetes-related complications as well as ER-stress. Therefore, we investigated the relationship between Sirtuin 1 (SIRT1) and ER stress-induced apoptosis in H9C2 cardiomyocyte.
Methods
Diabetic rats were established by a single intraperitoneal injection of streptozotocin (STZ; 50 mg/kg) with high-fat diet. For in vitro analysis, rat derived H9C2 cardiomyocytes were cultured. Cardiac function was assessed by Doppler, and SIRT1 as well as ER stress related protein expressions were measured by immunohistochemistry and western blotting. Cultured cells were exposed to advanced glycation end products (AGEs) (400 μg/mL) for inducing ER stress and apoptosis. Cell apoptosis were detected by flow cytometry.
Results
In vivo, ER stress was enhanced in the cardiomyocytes of diabetic rats without any treatments. A SIRT1 activator, resveratrol, could significantly restore cardiac function, reduce cardiomyocyte apoptosis, and ameliorate ER stress. In vitro, we showed that apoptosis and ER stress increased after AGE stimulation when SIRT1 expression was downregulated by short interfering RNA (siRNA) (p < 0.05). However, resveratrol (10 μM) restored SIRT1 levels in cardiomyocytes and markedly reduced ER stress-mediated apoptosis.
Conclusion
SIRT1 may attenuate ER stress-induced cardiomyocyte apoptosis via PERK/eIF2α, ATF6/CHOP, and IRE1α/JNK-mediated pathways. This study may provide insights into a novel underlying mechanism and a strategy for treating diabetic cardiomyopathy.
Elsevier
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