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beta-Sitosterol attenuates carbon tetrachloride-induced oxidative stress and chronic liver injury in rats

机译:β-谷甾醇衰减大鼠四氯化碳诱导的氧化胁迫和慢性肝损伤

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Chronic liver diseases are clinically silent and responsible for significant morbidity and mortality worldwide. beta-Sitosterol (BSS), major phytosterol in plants, has a wide spectrum of protective effect against various chronic ailments. We investigated the hepatoprotective effect of BSS against carbon tetrachloride (CCl4)-induced chronic liver injury in rats. Thirty rats were divided into five groups, with six animals in each group. Group I rats served as control while groups II, III, IV, and V rats were injected intraperitoneally with CCl4 (0.2 mL/100 g b.w. in olive oil (1:1)) for 7 consecutive weeks. After 7 weeks, group II rats were left without any treatments and served as CCl4 alone group, while groups III, IV, and V rats were treated with BSS 25 and 50 mg/kg b.w. and silymarin 100 mg/kg b.w. as oral post-treatments respectively, for the next 4 weeks. At the end of the experiment, hepatotoxicity marker enzymes in serum, oxidative stress, and fibrosis marker were analyzed. CCl4 administration caused significant elevation of marker enzymes of hepatotoxicity in serum and increased lipid peroxidation and fibrosis markers such as hydroxyproline, collagen, alpha-smooth muscle actin, vimentin, desmin, and matrix metalloproteinases 9 in liver tissue of rats. This treatment also caused a significant diminution of intracellular enyzmic antioxidants such as SOD and CAT in the liver tissue of rats. All the above adversities were significantly mitigated by the BSS post-treatments. The results suggest that BSS could have a hepatoprotective effect against oxidative stress-mediated CLD induced by CCl4.
机译:慢性肝病在临床上沉默,并负责全世界的显着发病率和死亡率。植物主要植物甾醇(BSS),植物主要植物甾醇,对各种慢性疾病具有广泛的保护作用。我们研究了BSS对四氯化碳(CCL4)的肝脏保护作用 - 致大鼠慢性肝损伤。将三十只大鼠分为五组,每组六只动物。第I族大鼠作为控制,同时II,III,IV和v大鼠连续7周内腹膜内注射(0.2mL / 100g B.W.在橄榄油(1:1))中。在7周后,留下II族大鼠没有任何治疗,并用作CCl4单独组,而III族,IV和v大鼠用BSS 25和50mg / kg B.W。和西里柳素100 mg / kg b.w.作为口腔治疗分别,未来4周。在实验结束时,分析了血清中的肝毒性标记酶,氧化应激和纤维化标志物。 CCL4给药导致血清中肝毒性的标记酶的显着升高,增加了大鼠肝组织中羟脯氨酸,胶原蛋白,α-平滑肌肌动蛋白,Vimentin,Desmin和基质金属蛋白酶9的脂质过氧化和纤维化标记物。这种治疗还引起大鼠肝组织中的细胞内依赖性抗氧化剂的显着减少。 BSS后处理显着减轻了上述所有逆境。结果表明,BSS可以对CCl4诱导的氧化应激介导的CLD具有肝保护作用。

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