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首页> 外文期刊>BioMed research international >Shengmai Injection Improved Doxorubicin-Induced Cardiomyopathy by Alleviating Myocardial Endoplasmic Reticulum Stress and Caspase-12 Dependent Apoptosis
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Shengmai Injection Improved Doxorubicin-Induced Cardiomyopathy by Alleviating Myocardial Endoplasmic Reticulum Stress and Caspase-12 Dependent Apoptosis

机译:通过缓解心肌内质网应激和Caspase-12依赖性细胞凋亡来改善多柔比蛋白诱导的心肌病

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Background. Apoptosis plays vital roles in the progression of doxorubicin-induced cardiomyopathy (DOX-CM). Endoplasmic reticulum stress (ER stress) could induce specific apoptosis by caspase-12 dependent pathway. Shengmai Injection (SMI), a famous Traditional Chinese Medicine, could alleviate the heart damage via inhibiting myocardial apoptosis. However, it is unknown whether SMI can alleviate ER stress and its specific apoptosis in the setting of DOX-CM. Objective. To explore the effects of SMI on heart function, myocardial ER stress, and apoptosis of DOX-CM rats. Methods. Rats with DOX-CM were treated by SMI. Heart function was assessed by echocardiography and brain natriuretic peptide. Myocardial apoptosis was detected by TUNEL assay. ER stress was assessed by detecting the expressions of GRP78 and caspase-12. Results. At the end of eight-week, compared to control, significant heart dysfunction happened in DOX group. The ratio of apoptotic cardiomyocytes and the expressions of GRP78 and caspase-12 increased significantly (P < 0.05). Compared to DOX group, the apoptotic ratio and the expressions of GRP78 and caspase-12 significantly decreased in DOX + SMI group (P < 0.05), accompanied with improved heart function. Conclusion. SMI could alleviate myocardial ER stress and caspase-12 dependent apoptosis, which subsequently helped to improve the heart function of rats with DOX-CM.
机译:背景。细胞凋亡在多柔比蛋白诱导的心肌病(DOX-CM)的进展中起着重要作用。内质网胁迫(ER应激)可以通过Caspase-12依赖性途径诱导特异性细胞凋亡。着名的中医胜迈注射(SMI)可以通过抑制心肌凋亡来缓解心脏损伤。然而,尚不清楚SMI是否可以减轻ER应激及其特异性凋亡,在DOX-CM的设置中。客观的。探讨SMI对心功能,心肌ER​​应激和DOX-CM大鼠凋亡的影响。方法。用DOX-CM的大鼠通过SMI治疗。通过超声心动图和脑利用肽评估心脏功能。 TUNEL测定检测心肌细胞凋亡。通过检测GRP78和Caspase-12的表达来评估ER应激。结果。在八周结束时,与对照相比,DOX集团发生了显着的心脏功能障碍。凋亡心细胞细胞和GRP78和Caspase-12的表达的比例显着增加(P <0.05)。与DOX组相比,凋亡比和GRP78和Caspase-12的表达在DOX + SMI组中显着降低(P <0.05),伴随着改进的心功能。结论。 SMI可以缓解心肌ER应激和Caspase-12依赖性凋亡,随后有助于改善DOX-CM大鼠的心脏功能。

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