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Celastrus Orbiculatus Thunb. Reduces Lipid Accumulation by Promoting Reverse Cholesterol Transport in Hyperlipidemic Mice

机译:Celastrus Orbiculatus Thunb。通过促进高脂血症小鼠的胆固醇逆向转运来减少脂质积累

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摘要

Previously, we found that Celastrus orbiculatus Thunb. (COT) decreases athero-susceptibility in lipoproteins and the aorta of guinea pigs fed a high-fat diet, and increases high-density lipoprotein (HDL). In the present study, we investigated the effect of COT in reducing lipid accumulation and promoting reverse cholesterol transport (RCT) in vivo and vitro. Healthy male mice were treated with high-fat diet alone, high-fat diet with COT (10.0 g/kg/d), or general fodder for 6 weeks. Serum levels of total cholesterol (TC), triglyceride (TG), HDL-C, non-HDL-C, and H-3-cholesterol in plasma, liver, bile, and feces were determined. Pathological changes and the levels of TC and TG in liver were examined. The expression of hepatic genes and protein associated with RCT were analyzed. COT administration reduced lipid accumulation in the liver, ameliorated the pathological changes, and lessened liver injury, the levels of TG, TC, and non-HDL-C in plasma were decreased significantly, and COT led to a significant increase in plasma HDL-C and apolipoprotein A (apoA1). H-3-cholesterol in plasma, liver, bile, and feces was also significantly increased in COT-treated mice compared to controls. Both mRNA and protein expression of SRB1, CYP7A1, LDLR, ATP-binding cassette transporters ABCA1, ABCG5, and LXR alpha were improved in COT-treated mice. An in vitro isotope tracing experiment showed that COT and its bioactive ingredients, such as celastrol, ursolic acid, oleanolic acid, and quercetin, significantly increased the efflux of H-3-cholesterol. They also increased the expression of SRB1, ABCA1, and ABCG1 significantly in macrophages. Our findings provided a positive role of COT in reducing lipid accumulation by promoting RCT. These effects may be achieved by activating the SRB1 and ABC transporter pathway and promoting cholesterol metabolism via the CYP7A1 pathway in vivo. The effective ingredients in vitro are celastrol, ursolic acid, oleanolic acid, and quercetin.
机译:先前,我们发现了Celastrus orbiculatus Thunb。 (COT)降低高脂饮食对豚鼠脂蛋白和主动脉的动脉粥样硬化敏感性,并增加高密度脂蛋白(HDL)。在本研究中,我们研究了COT在体内和体外减少脂质积累和促进胆固醇逆向转运(RCT)的作用。健康的雄性小鼠单独接受高脂饮食,COT(10.0 g / kg / d)的高脂饮食或普通饲料处理6周。测定血浆,肝,胆汁和粪便中的总胆固醇(TC),甘油三酸酯(TG),HDL-C,非HDL-C和H-3-胆固醇的血清水平。检查肝脏的病理变化以及TC和TG的水平。分析与RCT相关的肝基因和蛋白的表达。 COT给药减少了肝脏中的脂质蓄积,减轻了病理变化,减轻了肝损伤,血浆中TG,TC和非HDL-C的水平显着降低,COT导致血浆HDL-C显着增加和载脂蛋白A(apoA1)。与对照相比,COT处理的小鼠的血浆,肝,胆汁和粪便中的H-3-胆固醇也显着增加。在COT治疗的小鼠中,SRB1,CYP7A1,LDLR,ATP结合盒转运蛋白ABCA1,ABCG5和LXR alpha的mRNA和蛋白表达均得到改善。体外同位素示踪实验表明,COT及其生物活性成分(如Celastrol,熊果酸,齐墩果酸和槲皮素)显着增加了H-3-胆固醇的外排量。他们还显着增加了SRB1,ABCA1和ABCG1在巨噬细胞中的表达。我们的发现提供了COT通过促进RCT减少脂质蓄积的积极作用。这些作用可通过在体内激活SRB1和ABC转运蛋白途径并通过CYP7A1途径促进胆固醇代谢来实现。体外的有效成分是Celastrol,熊果酸,齐墩果酸和槲皮素。

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