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Gualou Xiebai Decoction a Traditional Chinese Medicine Prevents Cardiac Reperfusion Injury of Hyperlipidemia Rat via Energy Modulation

机译:中药瓜ou泻白汤通过能量调节预防高脂血症大鼠心脏再灌注损伤

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摘要

>Background: Gualou Xiebai Decoction (GLXB) is a classic prescription of Chinese medicine used for the treatment of cardiac problems. The present study was designed to explore the effect and mechanism of GLXB on ischemia/reperfusion (I/R) induced disorders in myocardial structure and function, focusing on the regulation of energy metabolism and the RhoA/ROCK pathway.>Methods: After hyperlipidemic rat model was established by oral administration of high fat diet, the rats were treated with GLXB for 6 weeks and subjected to 30 min occlusion of the left anterior descending coronary artery (LADCA) followed by 90 min reperfusion to elicit I/R challenge. Myocardial infarct size was assessed by Evans blue-TTC staining. Myocardial blood flow (MBF) and cardiac function were evaluated. Enzyme-linked immunosorbent assay was performed to examine the content of ATP, ADP, AMP, CK, CK-MB, LDH, cTnT, cTnI, and IL-6. Double staining of F-actin and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling was conducted to assess myocardial apoptosis. Expressions of ATP synthase subunit δ (ATP 5D), and RhoA and ROCK were determined by Western blotting.>Results: Administration with GLXB at high dose for 6 weeks protected heart against I/R-induced MBF decrease, myocardial infarction and apoptosis, ameliorated I/R-caused impairment of cardiac function and myocardial structure, restored the decrease in the ratio of ADP/ATP and AMP/ATP, and the expression of ATP 5D with inhibiting the expression of RhoA and ROCK.>Conclusions: Treatment with GLXB effectively protects myocardial structure and function from I/R challenge, possibly via regulating energy metabolism involving inactivation of RhoA/ROCK signaling pathway.
机译:>背景:瓜ou泻白汤(GLXB)是用于治疗心脏病的经典中药处方。本研究旨在探讨GLXB对缺血/再灌注(I / R)引起的心肌结构和功能障碍的作用和机制,重点是能量代谢的调节和RhoA / ROCK途径。>方法:< / strong>口服高脂饮食建立高脂血症大鼠模型后,将其用GLXB治疗6周,并闭塞左冠状动脉前降支(LADCA)30分钟,然后再灌注90分钟以诱发I / R挑战。心肌梗死面积通过伊文思蓝TTC染色评估。评估心肌血流量(MBF)和心脏功能。进行酶联免疫吸附测定以检查ATP,ADP,AMP,CK,CK-MB,LDH,cTnT,cTnI和IL-6的含量。对F-肌动蛋白和末端脱氧核苷酸转移酶介导的dUTP缺口末端标记进行双重染色以评估心肌细胞凋亡。通过蛋白质印迹法确定ATP合酶亚基δ(ATP 5D)以及RhoA和ROCK的表达。>结果:高剂量GLXB给药6周可保护心脏免受I / R诱导的MBF降低,心肌梗塞和细胞凋亡,减轻了I / R引起的心脏功能和心肌结构的损害,恢复了ADP / ATP和AMP / ATP的比率降低以及ATP 5D的表达,从而抑制了RhoA和ROCK的表达。 strong>结论:通过GLXB治疗可以有效地保护心肌结构和功能免受I / R挑战,这可能是通过调节涉及RhoA / ROCK信号通路失活的能量代谢来实现的。

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