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首页> 外文期刊>BMC Complementary and Alternative Medicine >Evaluation of anti-obesity activities of ethanolic extract of Terminalia paniculata bark on high fat diet-induced obese rats
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Evaluation of anti-obesity activities of ethanolic extract of Terminalia paniculata bark on high fat diet-induced obese rats

机译:榄仁树皮乙醇提取物对高脂饮食诱导的肥胖大鼠抗肥胖活性的评价

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Background The prevalence and severity of obesity and associated co-morbidities are rapidly increasing across the world. Natural products-based drug intervention has been proposed as one of the crucial strategies for management of obesity ailments. This study was designed to investigate the anti-obesity activities of ethanolic extract of Terminalia paniculata bark (TPEE) on high fat diet-induced obese rats. Methods LC-MS/MS analysis was done for ethanolic extract of T. paniculata bark. Male Sprague–Dawley (SD) rats were randomly divided into six groups of six each, normal diet fed (NC), high fat diet-fed (HFD), HFD+ orlistat (standard drug control) administered, and remaining three groups were fed with HFD?+?TPEE in different doses (100,150 and 200?mg/kg b. wt). For induction of obesity rats were initially fed with HFD for 9?weeks, then, (TPEE) was supplemented along with HFD for 42?days. Changes in body weight, body composition, blood glucose, insulin, tissue and serum lipid profiles, atherogenic index, liver markers, and expression of adipogenesis-related genes such as leptin, adiponectin, FAS, PPARgamma, AMPK-1alpha and SREBP-1c, were studied in experimental rats. Also, histopathological examination of adipose tissue was carried out. Results Supplementation of TPEE reduced significantly (P?Conclusions Together, the biochemical, histological and molecular studies unambiguously demonstrate the potential anti adipogenic and anti obesity activities of TPEE promoting it as a formidable candidate to develop anti obesity drug.
机译:背景技术肥胖症和相关合并症的患病率和严重性在世界范围内迅速增加。已经提出了基于天然产物的药物干预作为治疗肥胖症的关键策略之一。本研究旨在研究榄仁树皮乙醇提取物(TPEE)对高脂饮食诱导的肥胖大鼠的抗肥胖活性。方法采用LC-MS / MS法分析丹参皮的乙醇提取物。将雄性Sprague-Dawley(SD)大鼠随机分为六组,每组六只,分别为普通饮食喂养(NC),高脂饮食喂养(HFD),HFD +奥利司他(标准药物对照),其余三组分别喂养以不同剂量(100,150和200?mg / kg b。wt)的HFD?+?TPEE。为了诱导肥胖,首先给大鼠喂食HFD 9周,然后与HFD一起补充42天(TPEE)。体重,身体组成,血糖,胰岛素,组织和血清脂质谱,动脉粥样硬化指数,肝脏标志物以及与脂肪生成相关的基因(如瘦素,脂联素,FAS,PPARγ,AMPK-1alpha和SREBP-1c)的表达的变化,在实验大鼠中进行了研究。另外,进行了脂肪组织的组织病理学检查。结果TPEE的添加量显着减少(结论),生化,组织学和分子学研究明确表明TPEE具有潜在的抗脂肪形成和抗肥胖活性,从而使其成为开发抗肥胖药的强大候选者。

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