Shi Hui, Wang Liang, Fang Zhao-Hui, Ni Ying-Qun, Shen An-Lu, Liu Pei-Pei, Wang Xiang, Huang Jin-Ling
Nursing School,Anhui University of Chinese Medicine Hefei 230012,China.
School of Integrated Chinese Medicine and Western Medicine,Anhui University of Chinese Medicine Hefei 230012,China Institute of Integrated Chinese Medicine and Western Medicine,Anhui Academy of Chinese Medicine Hefei 230012,China.
Zhongguo Zhong Yao Za Zhi. 2019 Dec;44(23):5159-5165. doi: 10.19540/j.cnki.cjcmm.20191015.401.
Diabetic cardiomyopathy( DCM) is one of the major cardiovascular complications of diabetes mellitus. Based on the clinical efficacy of Danzhi Jiangtang Capsules( DJC) in the prevention and treatment of diabetes and its cardiovascular complications,both in vivo and in vitro methods were adopted to investigate its effect and underlying mechanism of protecting myocardial injury induced by diabetes. The type 2 diabetic rats were prepared by feeding high-energy food combined with streptozotin( STZ) injection,and the effects of DJC were observed by blood sugar,blood lipid,hemodynamic index,cardiac weight index and the change of cardiac pathological morphology. The protein expressions of TLR4,MyD88 and NF-κB p65 in myocardial tissue were detected and the possible mechanism was preliminarily analyzed. Besides this,DJC containing serum was prepared,H9 c2 cardiomyocyte induced by high sugar were studied to investigate the mechanism of TLR4/MyD88/NF-κB signaling pathway regulating cardiomyocyte injury and the therapeutic effect of DJC. The results demonstrated that fasting blood sugar,glycosylated hemoglobin,total cholesterol and glycerol triglyceride were significantly reduced( P<0. 01,P<0. 05). Cardiac weight index,left ventricle weight index,LVEDP and the protein expressions of TLR4,MyD88 and NF-κB p65 were significantly reduced( P<0. 01,P<0. 05). LVSP,+dp/dtmaxand-dp/dtmaxincreased significantly( P<0. 01,P< 0. 05). Moreover,the pathological damage of myocardial tissue in rats improved significantly. Meanwhile,the protein expressions of TLR4,MyD88 and NF-κB p65 in cardiomyocytes induced by high sugar were significantly inhibited( P<0. 01).It showed that DJC were effective in preventing and treating myocardial injury induced by diabetes and its mechanism may be related to the over-expression of TLR4/MyD88/NF-κB signaling pathway induced by high sugar.
糖尿病性心肌病(DCM)是糖尿病的主要心血管并发症之一。基于丹蛭降糖胶囊(DJC)在防治糖尿病及其心血管并发症方面的临床疗效,采用体内和体外方法研究其对糖尿病所致心肌损伤的保护作用及潜在机制。通过喂食高能食物联合注射链脲佐菌素(STZ)制备2型糖尿病大鼠,通过血糖、血脂、血流动力学指标、心脏重量指数及心脏病理形态变化观察DJC的作用。检测心肌组织中TLR4、MyD88和NF-κB p65的蛋白表达并初步分析可能机制。此外,制备含DJC血清,研究高糖诱导的H9 c2心肌细胞,探讨TLR4/MyD88/NF-κB信号通路调控心肌细胞损伤的机制及DJC的治疗作用。结果表明,空腹血糖、糖化血红蛋白、总胆固醇和甘油三酯显著降低(P<0.01,P<0.05)。心脏重量指数、左心室重量指数、左心室舒张末期压力以及TLR4、MyD88和NF-κB p65的蛋白表达显著降低(P<0.01,P<0.05)。左心室收缩压、+dp/dtmax和-dp/dtmax显著升高(P<0.01,P<0.05)。此外,大鼠心肌组织的病理损伤明显改善。同时,高糖诱导的心肌细胞中TLR4、MyD88和NF-κB p65的蛋白表达显著受到抑制(P<0.01)。结果表明,DJC对糖尿病所致心肌损伤具有防治作用,其机制可能与高糖诱导的TLR4/MyD88/NF-κB信号通路过度表达有关。