In Vivo Treatment with a Standardized Green Tea Extract Restores Cardiomyocyte Contractility in Diabetic Rats by Improving Mitochondrial Function through SIRT1 Activation.

Rocchina Vilella, Simona Izzo, Valeria Naponelli, Monia Savi, Leonardo Bocchi, Cristina Dallabona, Maria Carla Gerra, Donatella Stilli, Saverio Bettuzzi
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引用次数: 3

Abstract

Background. Green tea catechins are known to promote mitochondrial function, and to modulate gene expression and signalling pathways that are altered in the diabetic heart. We thus evaluated the effectiveness of the in vivo administration of a standardized green tea extract (GTE) in restoring cardiac performance, in a rat model of early streptozotocin-induced diabetes, with a focus on the underlying mechanisms. Methods. Twenty-five male adult Wistar rats were studied: the control (n = 9), untreated diabetic animals (n = 7) and diabetic rats subjected to daily GTE administration for 28 days (n = 9). Isolated ventricular cardiomyocytes were used for ex vivo measurements of cell mechanics and calcium transients, and molecular assays, including the analysis of functional protein and specific miRNA expression. Results. GTE treatment induced an almost complete recovery of cardiomyocyte contractility that was markedly impaired in the diabetic cells, by preserving mitochondrial function and energy availability, and modulating the expression of the sarcoplasmic reticulum calcium ATPase and phospholamban. Increased Sirtuin 1 (SIRT1) expression and activity substantially contributed to the observed cardioprotective effects. Conclusions. The data supported the hypothesis that green tea dietary polyphenols, by targeting SIRT1, can constitute an adjuvant strategy for counteracting the initial damage of the diabetic heart, before the occurrence of diabetic cardiomyopathy.

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标准绿茶提取物在体内通过SIRT1激活改善线粒体功能,恢复糖尿病大鼠心肌细胞收缩能力。
背景。众所周知,绿茶儿茶素可以促进线粒体功能,调节糖尿病心脏中改变的基因表达和信号通路。因此,我们在早期链脲佐菌素诱导的糖尿病大鼠模型中评估了标准绿茶提取物(GTE)在恢复心脏功能方面的有效性,并重点研究了其潜在机制。方法。研究了25只雄性成年Wistar大鼠:对照组(n = 9),未治疗的糖尿病大鼠(n = 7)和每天服用GTE的糖尿病大鼠(n = 9)。分离的心室心肌细胞用于细胞力学和钙瞬态的离体测量,并进行分子分析,包括功能蛋白和特异性miRNA表达的分析。结果。GTE治疗通过保持线粒体功能和能量可用性,以及调节肌浆网钙atp酶和磷蛋白的表达,诱导糖尿病细胞明显受损的心肌细胞收缩性几乎完全恢复。Sirtuin 1 (SIRT1)表达和活性的增加在很大程度上促进了观察到的心脏保护作用。结论。这些数据支持了一种假设,即绿茶膳食多酚通过靶向SIRT1,可以在糖尿病心肌病发生之前抵消糖尿病心脏的初始损伤。
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