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首页|期刊导航|海南医学院学报|姜黄素通过调节SIRT3/FOXO3a通路改善糖尿病心肌病的机制研究

姜黄素通过调节SIRT3/FOXO3a通路改善糖尿病心肌病的机制研究OACSTPCD

Mechanism of curcumin ameliorating diabetic cardiomyopathy by modulating the SIRT3/FOXO3a pathway

中文摘要英文摘要

目的:探究姜黄素对糖尿病心肌病小鼠的保护作用及对SIRT3/FOXO3a信号通路的影响.方法:将20只C57 BL/6小鼠随机分为正常对照组(Con组)、模型组(DCM组)、低剂量姜黄素组(LC组)、高剂量姜黄素组(HC组),除正常对照组外,其余各组均采用高脂高糖喂养联合腹腔注射链脲佐菌素(60 mg/kg)建立糖尿病心肌病模型.模型建立成功后,干预组分别予以高剂量(200 mg∙kg-1∙d-1)、低剂量(100 mg∙kg-1∙d-1)姜黄素灌胃,Con组、DCM组予以生理盐水灌胃.连续用药12周后行超声心动图检查测量小鼠心肌结构及功能变化,HE染色观察小鼠心肌组织病理表现;TUNEL法检测各组小鼠心肌细胞凋亡情况;检测心肌组织中脂质过氧化物丙二醛(MDA)的含量、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)的活性,DCFH-DA检测细胞内ROS水平;荧光定量PCR检测SIRT3、FOXO3a通路mRNA表达情况,Western blot法检测SIRT3、FOXO3a、Bcl2、Bax、Cleaved caspase-3蛋白表达.结果:与DCM组相比,姜黄素干预后,心脏彩超提示各项指标均有改善(P<0.05),TUNEL凋亡染色显示,凋亡率明显下降(P<0.05),HE染色提示细胞水肿,排列紊乱等变化明显改善,SIRT3、FOXO3a、Bcl2表达增加,Bax、Cleaved caspase-3表达减少,SOD、GSH-Px活性明显升高(P<0.05),MDA及ROS水平明显降低(P<0.05).结论:姜黄素对糖尿病心肌病小鼠具有心肌保护及抑制心肌重塑的作用,该作用机制可能与激活SIRT3/FOXO3a信号通路相关.

Objective:To investigate the protective effect of curcumin on mice with diabetic cardiomyopathy and its effect on SIRT3/FOXO3a signaling pathway.Methods:A total of twenty C57BL/6 mice were randomly assigned to four groups,with five mice in each group:the normal control group(Con group),the model group[diabetic cardiomyopathy(DCM)group],the low-dose curcumin group(LC group),and the high-dose curcumin group(HC group).Except for the Con group,the mice in other groups were fed with high-fat and high-glucose diet combined with intraperitoneal injection of streptozotocin(60 mg/kg)to estab-lish the DCM model.After the model was effectively established,the intervention group received high-dose(200 mg∙kg-1∙d-1)and low-dose(100 mg∙kg-1∙d-1)curcumin administration via gavage,while the Con group and DCM group received normal saline ad-ministration via gavage.Following 12 weeks of uninterrupted medication,echocardiography was conducted to assess the myocardi-al structure and function,and HE staining was performed to observe the pathological manifestations of myocardial tissue.The TU-NEL method was utilized to identify apoptosis in mouse cardiomyocytes within each group.The levels of lipid peroxidemalondial,superoxide dismutase,and glutathione peroxidase(GSH-Px)activities in myocardial tissue were assessed,while intracellular ROS levels were measured using DCFH-DA.The expression of mRNA in the SIRT3 and FOXO3a pathways was determined through fluorescence PCR,and the expression of SIRT3,FOXO3a,Bcl2,Bax,and Cleaved caspase-3 proteins was examined using the Western blot method.Results:In comparison to the DCM group,following curcumin intervention,all the indices dem-onstrated amelioration in cardiac ultrasound(P<0.05).TUNEL apoptosis staining revealed a significant reduction in the rate of apoptosis(P<0.05).Additionally,HE staining exhibited notable improvement in cellular edema,disorder in arrangement,the ex-pression of SIRT3,FOXO3a,and Bcl2 was enhanced,while the expression of Bax and Cleaved caspase-3 was diminished.More-over,the activity of superoxide dismutase and GSH-Px exhibited a significant increase(P<0.05),whereas the levels of lipid per-oxidemalondial and ROS were notably decreased(P<0.05).Conclusion:Curcumin has myocardial protective effect and inhibition of ventricular remodeling in mice with diabetic cardiomyopathy,and the mechanism of action may be related to the activation of SIRT3/FOXO3a signaling pathway.

李星;钟毅;陈雪

西南医科大学附属医院心血管内科,四川 泸州 646000

中医学

姜黄素糖尿病心肌病SIRT3氧化应激

CurcuminDiabetic cardiomyopathySIRT3Oxidative stress

《海南医学院学报》 2024 (006)

401-406 / 6

This study was supported by Luzhou Municipal People's Government-Southwest Medical University Strategic Cooperation Project(2018-LZXNYD ZK48) 泸州市人民政府-西南医科大学战略合作项目(2018-LZXNYD ZK48)

10.13210/j.cnki.jhmu.20231129.003

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