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Therapeutic effect of bone marrow mesenchymal stem cells in a rat model of carbon tetrachloride induced liver fibrosis

机译:骨髓间充质干细胞在四氯化碳诱导肝纤维化大鼠模型中的疗效作用

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Background Liver fibrosis is a major medical problem with high mortality and morbidity rates where the formation of regenerative nodules and cirrhosis leads to loss of liver function and may result in the development of hepatocellular carcinoma. Bone marrow Mesenchymal stem cells (BM-MSCs) have drawn attention as a novel approach for treatment of liver fibrosis. This study aimed to evaluate the therapeutic effect of BM-MSCs on the liver structure in carbon tetrachloride (CClsub4/sub) induced liver fibrosis in male rats relative to resveratrol and Silybum marianum as standard drugs derived from herbal plants. Methods Fifty adult male albino rats (Sprague Dawley strain; 180–220?g mean body weight) were purchased from the Laboratory Animal Unit in the Nile Center of Experimental Research, Mansoura, Egypt. Liver function were determined, isolation and preparation of BM- MSCs and detection of cell-surface markers by flow cytometry. Results Animals exposed to CClsub4/sub developed liver injury characterized by significant increase of liver enzymes, malondialdehyde (MDA), tumor necrosis factor alpha (TNFα), and CYP450, inhibition of antioxidant enzymes, and decreased albumin. Treatment with stem cells enhanced liver state more effectively than resveratrol and S. marianum . It significantly decreased AST, ALT, ALP, MDA, TNF-α, and CYP450 and increased albumin, SOD, GSH, GST, and CAT. Histopathological study and atomic force microscope results confirmed the therapeutic effects of MSCs. Conclusions BM-MSCs could restore liver structure and function in CCLsub4/sub induced liver fibrosis rat model, ameliorating the toxicity of CClsub4/sub and improving liver function tests.
机译:背景技术肝纤维化是具有高死亡率和发病率的主要医学问题,其中再生结节和肝硬化形成损失肝功能,并且可能导致肝细胞癌的发育。骨髓间充质干细胞(BM-MSCs)被引起注意作为治疗肝纤维化的新方法。该研究旨在评估BM-MSCs对四氯化物(CCL 4 )肝纤维化的肝脏结构的治疗效果,相对于白藜芦醇和Silvbum Marianum作为来自草药植物的标准药物。方法采购五十六大鼠(Sprague Dawley菌株; 180-220 ~g均值)从尼罗河实验研究中心的实验室动物单位购买了Mansoura,埃及的实验室动物单位。通过流式细胞术确定,分离和制备BM-MSCs的分离和制备细胞表面标志物。结果暴露于CCL 4 的动物,其特征在于肝酶,丙二醛(MDA),肿瘤坏死因子α(TNFα)和CYP450的显着增加,抗氧化酶的抑制和降低的白蛋白。用干细胞治疗比白藜芦醇和S. Marianum更有效地治疗肝脏状态。它显着降低了AST,ALT,ALP,MDA,TNF-α和CYP450,并增加白蛋白,SOD,GSH,GST和猫。组织病理学研究和原子力显微镜结果证实了MSCs的治疗效果。结论BM-MSC可以恢复肝脏结构和CCL 4 诱导肝纤维化大鼠模型中的功能,改善CCL 4 提高肝功能试验的毒性。

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