Effects of valsartan on heart failure with dilated cardiomyopathy myocardial apoptosis associated protein.docVIP
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Effects of valsartan on heart failure with dilated cardiomyopathy myocardial apoptosis associated protein
Of: Zhang Xin Zhang Mu Su Zhaoliang win for Chen Jianhua Zhang Guohui Li Weidong Yin Chunyang
[Abstract] Objective To observe the valsartan (Val) of dilated cardiomyopathy (DCM) heart failure, myocardial apoptosis related proteins. Methods SD rats were randomized into 3 groups: model group (DCM group, n = 15), Val group (DCM + Val group, n = 15), the control group (C group, n = 10). DCM group and DCM + Val groups were given intraperitoneal injection of doxorubicin, DCM + Val were given valsartan ig .8 w, the use of Western blotting, immunohistochemistry myocardial tissue expression of apoptosis-related protein, TUNEL assay apoptosis index (CMAI). Results Western blot showed, DCM group and DCM + Val group in rat heart VDAC, Smac protein relative expression level was significantly higher than C group (all P lt;0.05, compared with the DCM, DCM + Val rats, myocardial tissue levels of both proteins was significantly decreased ( P lt;0.05. immunohistochemistry showed that, DCM group and DCM + Val groups VDAC, Smac-positive cells was significantly more than the C group, compared with the DCM, DCM + Val groups of two protein-positive cells was significantly reduced. TUNEL results showed that, DCM group and DCM + Val CMAI rats compared with C increased significantly (all P lt;0.05, compared with the DCM, DCM + Val rats CMAI decreased, but the difference was not statistically significance (Pgt; 0.05. Conclusion Val DCM heart failure on myocardial cell apoptosis was inhibited.
[Keywords:] Valsartan, dilated cardiomyopathy, apoptosis
National Institutes of Health (NIH formulate strategies for cardiovascular disease, to encourage respect from apoptosis, the heart failure and dilated cardiomyopathy (DCM) of the molecular and cellular mechanisms of joint research (1). Angiotensin 1 receptor (angiotensin II type 1 receptor, AT1R anta
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