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首页> 外文期刊>Oxidative Medicine and Cellular Longevity >Antifibrogenic Influence of Mentha piperita L. Essential Oil against CCl4-Induced Liver Fibrosis in Rats
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Antifibrogenic Influence of Mentha piperita L. Essential Oil against CCl4-Induced Liver Fibrosis in Rats

机译:薄荷油对CCl4诱导的大鼠肝纤维化的抗纤维化作用

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Essential oils of some aromatic plants provide an effective nonmedicinal option to control liver fibrosis. Mentha piperita L. essential oil (MPEO) have been reported to possess protective effects against hepatotoxicity. However, its effect against liver fibrosis remains unknown. The present study investigated the antifibrogenic potential of MPEO and its underlying mechanisms. Forty male rats divided into 4 groups were used group 1 served as normal control, group 2 (liver fibrosis) received CCl4 (2.5 mL/kg, IP, twice weekly) for 8 weeks, group 3 concurrently received CCl4 plus MPEO (50 mg/kg, IP, daily, from the 3rd week), and group 4 received MPEO only. MPOE significantly improved the liver injury markers, lipid peroxidation (LPO), antioxidant capacity, CYP2E1 gene expressionand liver histology. Furthermore, MPOE ameliorated liver fibrosis as evidenced by the reduced expression of desmin, α-smooth muscle actin (α-SMA), transforming growth factor-β1 (TGF-β1), and SMAD3 proteins. In addition, MPOE counteracted the p53 upregulation induced by CCl4 at both mRNA and protein levels. In conclusion, MPOE could effectively attenuate hepatic fibrosis mainly through improving the redox status, suppressing p53 and subsequently modulating TGF-β1 and SMAD3 protein expression. These data promote the use of MPOE as a promising approach in antifibrotic therapy.
机译:一些芳香植物的精油为控制肝纤维化提供了有效的非药用选择。据报道薄荷薄荷精油(MPEO)具有抗肝毒性的保护作用。然而,其抗肝纤维化的作用仍未知。本研究调查了MPEO的抗纤维化潜力及其潜在机制。 40只雄性大鼠分为4组,第1组作为正常对照组,第2组(肝纤维化)接受CCl4(2.5 mL / kg,IP,每周两次),共8周,第3组同时接受CCl4加MPEO(50μmg/ ml)。从第3周开始,每天IP,每天3 kg)和第4组仅接受MPEO。 MPOE显着改善了肝损伤标志物,脂质过氧化(LPO),抗氧化能力,CYP2E1基因表达和肝组织学。此外,结蛋白,α-平滑肌肌动蛋白(α-SMA),转化生长因子-β1(TGF-β1)和SMAD3蛋白的表达降低证明了MPOE改善了肝纤维化。此外,MPOE在mRNA和蛋白质水平上均抵消了CCl4诱导的p53上调。总之,MPOE可以主要通过改善氧化还原状态,抑制p53并随后调节TGF-β1和SMAD3蛋白表达来有效减轻肝纤维化。这些数据促进了MPOE在抗纤维化治疗中的应用。

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