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首页> 外文期刊>Journal of food and drug analysis >Hepatoprotective effects of kaempferol 3-O-rutinoside and kaempferol 3-O-glucoside from Carthamus tinctorius L. on CCl4-induced oxidative liver injury in mice
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Hepatoprotective effects of kaempferol 3-O-rutinoside and kaempferol 3-O-glucoside from Carthamus tinctorius L. on CCl4-induced oxidative liver injury in mice

机译:红花山emp酚3-O-芸香糖苷和山fer酚3-O-葡糖苷对CCl4诱导的小鼠氧化性肝损伤的肝保护作用

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摘要

Abstract Safflower (Carthamus tinctorius L.) is a traditional medicinal and edible herb with a long history of use in China. In this study, a model of hepatotoxicity induced by carbon tetrachloride (CCl4) in mice was used to investigate the hepatoprotective effects of kaempferol 3-O-rutinoside (K-3-R) and kaempferol 3-O-glucoside (K-3-G), two kaempferol glycosides isolated from C. tinctorius L. K-3-R and K-3-G, at doses of 200?mg/kg and 400?mg/kg, were given orally to male mice once/d for 7 days before they received {CCl4} intraperitoneally. Our results showed that K-3-R and K-3-G treatment increased the level of total protein (TP) and prevented the CCl4-induced increases in serum aspartate aminotransferase (AST), serum alkaline phosphatase (ALP), and hepatic malondialdehyde (MDA) levels. Additionally, mice treated with K-3-R and K-3-G had significantly restored glutathione (GSH) levels and showed normal catalase (CAT) and superoxide dismutase (SOD) activities, compared to CCl4-treated mice. K-3-R and K-3-G also mitigated the CCl4-induced liver histological alteration, as indicated by histopathological evaluation. These findings demonstrate that K-3-R and K-3-G have protective effects against acute CCl4-induced oxidative liver damage.
机译:摘要红花(Carthamus tinctorius L.)是在中国具有悠久历史的传统药用和食用草药。在这项研究中,使用四氯化碳(CCl4)诱导的小鼠肝毒性模型来研究山emp酚3-O-芸苔苷(K-3-R)和山ka酚3-O-葡糖苷(K-3-)的肝保护作用。 G),分别以200?mg / kg和400?mg / kg的剂量口服从C. tinctorius L. K-3-R和K-3-G中分离得到的两种山emp酚糖苷一次,每天一次。他们腹腔接受{CCl4}的7天前。我们的结果表明,K-3-R和K-3-G处理可增加总蛋白(TP)的水平,并阻止CCl4诱导的血清天冬氨酸转氨酶(AST),血清碱性磷酸酶(ALP)和肝丙二醛水平的升高(MDA)级别。此外,与CCl4处理的小鼠相比,用K-3-R和K-3-G处理的小鼠具有显着恢复的谷胱甘肽(GSH)水平,并显示出正常的过氧化氢酶(CAT)和超氧化物歧化酶(SOD)活性。如组织病理学评估所示,K-3-R和K-3-G还减轻了CCl4诱导的肝脏组织学改变。这些发现表明,K-3-R和K-3-G对急性CCl4诱导的氧化性肝损伤具有保护作用。

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