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白藜芦醇通过预防非对称二甲基精氨酸引起的过氧化物酶体增殖物激活受体-γ共激活因子-1α乙酰化来改善糖尿病性心肌病。

Resveratrol improves diabetic cardiomyopathy by preventing asymmetric dimethylarginine-caused peroxisome proliferator-activated receptor-γ coactivator-1α acetylation.

机构信息

Innovation Centre for Advanced Interdisciplinary Medicine, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510700, Guangdong, China; Guangzhou Institute of Snake Venom Research, Guangzhou Medical University, Guangzhou, 511436, Guangdong, China; Department of Pharmacy, The Third Xiangya Hospital of Central South University, Changsha, 410013, Hunan, China.

Innovation Centre for Advanced Interdisciplinary Medicine, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510700, Guangdong, China; Guangzhou Institute of Snake Venom Research, Guangzhou Medical University, Guangzhou, 511436, Guangdong, China.

出版信息

Eur J Pharmacol. 2022 Dec 5;936:175342. doi: 10.1016/j.ejphar.2022.175342. Epub 2022 Oct 29.

Abstract

OBJECTIVES

Cardiac protection of resveratrol is related to the improvement of mitochondrial function through sirtuin1 (SIRT1) activation and peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α) deacetylation. Asymmetric dimethylarginine (ADMA) as an endogenous inhibitor of nitric oxide synthases is associated with diabetic cardiovascular complications and has a cross-talk with lysine acetylation. This study was to determine whether resveratrol reverses ADMA's pathogenic role in diabetic cardiomyopathy and elucidate the underlying mechanisms in type 2 diabetic (T2DM) rats and cardiomyocytes.

METHODS

T2DM Rats were induced by high-fat diet plus small-dose streptozotocin injection (35 mg/kg). Resveratrol was given by gavage (50 mg/kg/d) to some rats for 16w. Cardiac function was measured by echocardiography, and PGC-1α acetylation was detected by immunoprecipitation. Mitochondrial DNA and ATP contents were analyzed to evaluate mitochondrial biogenesis and function.

RESULTS

Endogenous ADMA accumulation and its signal disorders were associated with cardiac and mitochondrial dysfunctions in accompany with increased PGC-1α acetylation and decreased PGC-1α expression in the myocardium of T2DM rats compared with control rats. Resveratrol treatment attenuated ADMA accumulation, cardiac and mitochondrial dysfunctions in parallel with reversing altered PGC-1α expression and acetylation in the myocardium of T2DM rats. Exogenous ADMA not only reproduced mitochondrial dysfunction and cardiac hypertrophy but also reduced PGC-1α expression and enhanced PGC-1α acetylation in accompany of down-regulating SIRT1 and up-regulating acetyltransferase expression, all of which could be prevented by resveratrol pretreatment in cardiomyocytes.

CONCLUSIONS

These results indicate that ADMA promotes PGC-1α acetylation as a potential therapeutic target for resveratrol of management diabetic cardiomyopathy in T2DM rats.

摘要

目的

白藜芦醇通过激活 SIRT1(沉默调节蛋白 1)和过氧化物酶体增殖物激活受体-γ共激活因子 1α(PGC-1α)去乙酰化来改善线粒体功能,从而起到心脏保护作用。作为一氧化氮合酶的内源性抑制剂,不对称二甲基精氨酸(ADMA)与糖尿病心血管并发症有关,并与赖氨酸乙酰化相互作用。本研究旨在确定白藜芦醇是否能逆转 ADMA 在糖尿病心肌病中的致病作用,并阐明其在 2 型糖尿病(T2DM)大鼠和心肌细胞中的潜在机制。

方法

通过高脂肪饮食加小剂量链脲佐菌素(35mg/kg)注射诱导 T2DM 大鼠。给予部分大鼠白藜芦醇灌胃(50mg/kg/d)16w。通过超声心动图测量心功能,免疫沉淀检测 PGC-1α 乙酰化。分析线粒体 DNA 和 ATP 含量以评估线粒体生物发生和功能。

结果

与对照组大鼠相比,T2DM 大鼠心肌中内源性 ADMA 积累及其信号紊乱与心脏和线粒体功能障碍有关,同时伴有 PGC-1α 乙酰化增加和表达减少。白藜芦醇治疗可减轻 ADMA 积累,改善 T2DM 大鼠的心脏和线粒体功能障碍,同时逆转 T2DM 大鼠心肌中改变的 PGC-1α 表达和乙酰化。外源性 ADMA 不仅复制了线粒体功能障碍和心脏肥大,还降低了 PGC-1α 的表达,增强了其乙酰化,同时下调了 SIRT1 表达,上调了乙酰转移酶表达,所有这些都可以被心肌细胞中白藜芦醇预处理所预防。

结论

这些结果表明,ADMA 促进 PGC-1α 乙酰化,作为白藜芦醇治疗 T2DM 大鼠糖尿病心肌病的潜在治疗靶点。

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