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首页> 外文期刊>Nutrients >Total Flavonoids from Rosa laevigata Michx Fruit Ameliorates Hepatic Ischemia/Reperfusion Injury through Inhibition of Oxidative Stress and Inflammation in Rats
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Total Flavonoids from Rosa laevigata Michx Fruit Ameliorates Hepatic Ischemia/Reperfusion Injury through Inhibition of Oxidative Stress and Inflammation in Rats

机译:蔷薇果中的总黄酮可通过抑制大鼠的氧化应激和炎症减轻肝缺血/再灌注损伤

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The effects of total flavonoids (TFs) from Rosa laevigata Michx fruit against liver damage and cerebral ischemia/reperfusion (I/R) injury have been reported, but its action on hepatic I/R injury remains unknown. In this work, the effects and possible mechanisms of TFs against hepatic I/R injury were examined using a 70% partial hepatic warm ischemia rat model. The results demonstrated TFs decreased serum aspartate transaminase (AST), alanine aminotransferase (ALT), myeloperoxidase (MPO), and lactate dehydrogenase (LDH) activities, improved liver histopathology and ultrastructure through hematoxylin-eosin (HE) staining and electron microscope observation. In addition, TFs significantly decreased malondialdehyde (MDA) and increased the levels of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), which indicated that TFs alleviated oxidative stress caused by I/R injury. RT-PCR results proved that TFs downregulated the gene levels of inflammatory factors including interleukin-1 beta (IL-1β), interleukin-1 (IL-6), and tumor necrosis factor alpha (TNF-α). Further research indicated that TF-induced hepatoprotection was completed through inhibiting TLR4/MyD88 and activating Sirt1/Nrf2 signaling pathways. Blockade of the TLR4 pathway by TFs inhibited NF-κB and AP-1 transcriptional activities and inflammatory reaction. Activation of Sirt1/Nrf2 pathway by TFs increased the protein levels of HO-1 and GST to improve oxidative stress. Collectively, these findingsconfirmed the potent effects of TFs against hepatic I/R injury, which should be developed as a candidate for the prevention of this disease.
机译:曾报道过蔷薇果总黄酮对肝脏损伤和脑缺血/再灌注(I / R)损伤的作用,但其对肝I / R损伤的作用尚不清楚。在这项工作中,使用70%的部分肝脏温暖缺血大鼠模型检查了TFs对肝脏I / R损伤的影响及其可能的机制。结果表明,TFs通过苏木精-曙红(HE)染色和电子显微镜观察,降低了血清天冬氨酸转氨酶(AST),丙氨酸转氨酶(ALT),髓过氧化物酶(MPO)和乳酸脱氢酶(LDH)的活性,改善了肝脏组织病理学和超微结构。此外,TFs显着降低了丙二醛(MDA)并增加了超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)的水平,这表明TFs减轻了I / R损伤引起的氧化应激。 RT-PCR结果证明,TFs下调了炎症因子的基因水平,包括白介素-1β(IL-1β),白介素-1(IL-6)和肿瘤坏死因子α(TNF-α)。进一步的研究表明,TF诱导的肝保护作用通过抑制TLR4 / MyD88和激活Sirt1 / Nrf2信号通路而完成。 TF阻断TLR4途径可抑制NF-κB和AP-1的转录活性以及炎症反应。 TF对Sirt1 / Nrf2途径的激活增加了HO-1和GST的蛋白质水平,从而改善了氧化应激。总的来说,这些发现证实了TFs对肝I / R损伤的有效作用,应将其开发为预防该疾病的候选药物。

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