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首页> 外文期刊>Journal of King Saud University >Moringa oleifera leaves ethanolic extract ameliorates high fat diet-induced obesity in rats
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Moringa oleifera leaves ethanolic extract ameliorates high fat diet-induced obesity in rats

机译:辣木oleifera 叶子乙醇提取物改善高脂饮食诱导的大鼠肥胖

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Obesity is one of the major health problems worldwide. This study aimed to evaluate anti-obesity potential ofMoringa oleiferaleaves ethanolic extract (MOE) in rats. Fifty male Wistar rats of 100–120?g body weight (BW) were randomly allocated to 5 groups (n?=?10) as follows: Control (Cont group) was fed basal diet. Group II (M-group) was fed basal diet and orally given MOE (300?mg/kg BW) for 14?weeks. Group III (HFD-group) was fed a high fat diet (HFD) for 14?weeks. Group IV (HFD?+?M-group) was fed HFD and given MOE as in group II. Group V (HFD then M-group) was fed HFD for 8?weeks then basal diet and received MOE as group II for another 6?weeks. Phytochemical analysis of MOE revealed the presence of ferulic acid, kaempferol, cinnamic acid, ellagic acid, naringenin, rutin, caffeic acid, chlorogenic acid, methyl gallate gallic acid, catechin, vanillin, caffeic acid, coumaric acid, syringic acid, and pyrocatechol. Feeding HFD significantly elevated the serum level of total cholesterol, triacylglycerol, low density lipoprotein, glucose, insulin, leptin, malondialdehyde; elevated hepatic expression of nuclear factor-kappa β (NFκβ) and induced various histopathological changes in liver. Moreover, it lowered serum levels of high-density lipoprotein, adiponectin, serum superoxide dismutase activity and catalase activity compared to control group. Interestingly, administration of MOE to HFD-fed animals either concurrently (HFD?+?M group), or after induction of obesity (HFD then M group), significantly reversed the HFD-induced increase in BW and visceral fat mass, hyperglycemia, hyperleptinemia, hyperinsulinemia, hypoadiponectinemia, dyslipidemia; increased lipid peroxidation, hepatic NFκβ protein expression; restored normal hepatic tissue architecture and antioxidant activity. In conclusion, MOE ameliorated HFD-induced obesity, adiposity, serum biochemical and hepatic histopathological alterations. MOE accomplished these effects mostly through the anti-obesity, anti-inflammatory, anti-oxidant activities of its various bioactive identified compounds.
机译:肥胖是全世界的主要健康问题之一。本研究旨在评估偏美的抗肥胖潜力,对大鼠的乙醇提取物(MOE)进行抗肥胖潜力。 5-120°G体重(BW)的五十雄幼虫大鼠随机分配给5组(n?= 10),如下:对照(CONT组)喂养基础饮食。 II组(M-GROUP)是基础饮食和口服婴儿(300μmg/ kg bw)的14℃。 III组(HFD-GROUP)喂养高脂饮食(HFD)14个?周。第四组(HFD?+ + M-GROUP)被喂养HFD和赋予II组的MOE。 v组(HFD然后M-GROUP)被喂食HFD 8?周,然后将基础饮食和接受MOE作为II族另外6次。 MOE的植物化学分析揭示了阿魏酸,Kaempferol,肉桂酸,鞣花酸,芽孢素素,芦丁,咖啡酸,绿原酸,甲状腺蛋白,无碱酸,儿茶素,香草醛,咖啡酸,香豆酸,注射酸和PyrocateChol。饲料HFD显着升高了总胆固醇,三酰基甘油,低密度脂蛋白,葡萄糖,胰岛素,瘦蛋白,丙二醛的血清水平;核因子-Kappaβ(NFκβ)的肝脏表达升高,诱导了肝脏的各种组织病理学变化。此外,与对照组相比,它降低了高密度脂蛋白,脂肪蛋白,血清超氧化物歧化酶活性和过氧化氢酶活性的血清水平。有趣的是,萌发母猪同时(HFD?+ΔM组)或诱导肥胖症(HFD然后M组)后施用,显着逆转了BW和内脏脂肪质量,高血糖,高层胰蛋白症的HFD诱导的增加,高胰岛素血症,低传钙癌血症,血脂血症;增加脂质过氧化,肝NFκβ蛋白表达;恢复正常肝组织结构和抗氧化活性。总之,MOE改善了HFD诱导的肥胖,肥胖,血清生物化学和肝细胞病理学改变。 MOE主要通过其各种生物活性鉴定的化合物的抗肥胖,抗炎,抗氧化活性完成这些效果。

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