首页> 美国卫生研究院文献>Oncotarget >Protective effect of Ginkgo biloba leaves extract EGb761 on myocardium injury in ischemia reperfusion rats via regulation of TLR-4/NF-κB signaling pathway
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Protective effect of Ginkgo biloba leaves extract EGb761 on myocardium injury in ischemia reperfusion rats via regulation of TLR-4/NF-κB signaling pathway

机译:银杏叶提取物银杏叶提取物EGB761通过调节TLR-4 /NF-κB信号通路对缺血再灌注大鼠心肌的保护作用

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摘要

Beneficial actions of EGb 761 against ischemia/reperfusion (I/R) injury in lung, brain and renal ischemia have been described. However, the relationship between EGb 761 and signal molecules in myocardial ischemia reperfusion has not been well elucidated. In this study, we investigated the effects and mechanism of EGb 761 preconditioning on anti-myocardial I/R injuries in vivo. Meanwhile, their potential anti-oxidative stress and anti-inflammation effect were assessed. Hemodynamic parameters were monitored as left ventricular systolic pressure, LV end-diastolic pressure and maximal rate of increase and decrease of left ventricular pressure (dP/dtmax). The oxidative stress indicators and inflammatory factors were also evaluated. Western blot method was used for analysis of toll-like receptor 4 (TLR4), p-TLR4, nuclear factor-κB (NF-κB), p-NF-κB p65, Bax and Bcl-2 protein expressions. EGb 761 significantly improved cardiac function, decreased levels of creatine kinase, aspartate aminotransferase and lactate dehydrogenase. EGb 761 also restrained the oxidative stress related to myocardial ischemia injury as evidenced by decreased malondialdehyde, superoxide dismutase, catalase, glutathione-peroxidase, glutathione reductase activity. Meanwhile, the inflammatory cascade was inhibited as evidenced by decreased cytokines such as tumor necrosis factor-α, interleukin-6 and interleukin-1β. Our results still showed that EGb 761 pretreatment significantly decrease the level of cleaved Bax, and increase the level of Bcl-2 in rats subjected to I/R injury. Simultaneously, the expressions of myocardial TLR4 and NF-κB were significantly decreased. It can be concluded that EGb 761 pretreatment was protected against myocardium I/R injury by decreasing oxidative stress, repressing inflammatory cascade in vivo and inhibiting TLR4/NF-κB pathway.
机译:已经描述了EGb 761对肺,脑和肾缺血中的缺血/再灌注(I / R)损伤的有益作用。然而,EGb 761与心肌缺血再灌注信号分子之间的关系尚未得到很好的阐明。在这项研究中,我们调查了EGb 761预处理对体内抗心肌I / R损伤的作用和机制。同时,评估了它们潜在的抗氧化应激和抗炎作用。监测血流动力学参数,如左心室收缩压,左室舒张末压和左室压力的最大增减率(dP / dtmax)。还评估了氧化应激指标和炎性因子。 Western印迹法用于分析toll样受体4(TLR4),p-TLR4,核因子-κB(NF-κB),p-NF-κBp65,Bax和Bcl-2蛋白表达。 EGb 761可显着改善心脏功能,降低肌酸激酶,天冬氨酸转氨酶和乳酸脱氢酶的水平。 EGb 761还抑制了与心肌缺血相关的氧化应激,丙二醛,超氧化物歧化酶,过氧化氢酶,谷胱甘肽过氧化物酶,谷胱甘肽还原酶活性降低证明了这一点。同时,如肿瘤坏死因子-α,白介素-6和白介素-1β等细胞因子减少所证明,炎症级联受到抑制。我们的结果仍然表明,EGB 761预处理可显着降低I / R损伤大鼠体内裂解的Bax水平,并提高Bcl-2水平。同时,心肌TLR4和NF-κB的表达明显降低。可以得出结论,EGB 761预处理可通过降低氧化应激,抑制体内炎症级联反应和抑制TLR4 /NF-κB途径来防止心肌I / R损伤。

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