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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反向胆固醇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:以前,我们发现CelAstrus Orbiculatus Thunb。 (COT)降低脂蛋白的静脉曲张敏感性,豚鼠的主动脉喂养高脂饮食,并增加高密度脂蛋白(HDL)。在本研究中,我们研究了COT在减少脂质积累和促进体外抗胆固醇转运(RCT)的作用。单独用高脂饮食治疗健康的雄性小鼠,用婴儿床(10.0g / kg / d)或一般饲料为6周。确定血浆,甘油三酯(Tg),HDL-C,非HDL-C和血浆中的血清水平,血浆,肝,胆汁和粪便中的HDL-C,非HDL-C和H-3-胆固醇。研究了肝脏中TC和TG水平和TC和TG水平。分析了与RCT相关的肝基因和蛋白质的表达。婴儿床施用减少肝脏中的脂质积累,改善了病理变化,降低了肝损伤,血浆中的Tg,Tc和非HDL-C水平显着降低,并且COT导致血浆HDL-C的显着增加和载脂蛋白a(apoa1)。与对照组相比,血浆,肝脏,胆汁和粪便中的血浆,肝脏,胆汁和粪便中的H-3-胆固醇也显着增加。 SRB1,CYP7A1,LDLR,ATP结合盒转运蛋白ABCA1,ABCG5和LXRα的MRNA和蛋白表达均在COT处理的小鼠中得到改善。体外同位素追踪实验表明,婴儿床及其生物活性成分,如Celastrol,熊糖酸,葡糖醇和槲皮素,显着增加了H-3-胆固醇的流出。它们还在巨噬细胞中显着增加了SRB1,ABCA1和ABCG1的表达。我们的研究结果提供了COT通过促进RCT降低脂质积累的积极作用。这些效果可以通过激活SRB1和ABC转运途径并通过体内CYP7A1途径促进胆固醇代谢来实现。体外的有效成分是Celastrol,熊糖酸,葡糖醇和槲皮素。

著录项

  • 来源
    《Lipids》 |2016年第6期|共16页
  • 作者单位

    Taishan Med Univ Shandong Univ Key Lab Atherosclerosis Tai An 271000 Shandong Peoples R China;

    Taishan Med Univ Shandong Univ Key Lab Atherosclerosis Tai An 271000 Shandong Peoples R China;

    Taishan Med Univ Shandong Univ Key Lab Atherosclerosis Tai An 271000 Shandong Peoples R China;

    Taishan Med Univ Shandong Univ Key Lab Atherosclerosis Tai An 271000 Shandong Peoples R China;

    Shandong Agr Univ Tai An 271000 Shandong Peoples R China;

    Taishan Med Univ Shandong Univ Key Lab Atherosclerosis Tai An 271000 Shandong Peoples R China;

    Taishan Med Univ Shandong Univ Key Lab Atherosclerosis Tai An 271000 Shandong Peoples R China;

    Taishan Med Univ Shandong Univ Key Lab Atherosclerosis Tai An 271000 Shandong Peoples R China;

    Taishan Med Univ Shandong Univ Key Lab Atherosclerosis Tai An 271000 Shandong Peoples R China;

    Taishan Med Univ Shandong Univ Key Lab Atherosclerosis Tai An 271000 Shandong Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

    Celastrus orbiculatus Thunb.; Lipid accumulation; Reverse cholesterol transport; Cholesterol efflux; Isotope tracing;

    机译:Celastrus Orbiculatus Thunb。;脂质积累;反向胆固醇转运;胆固醇流出;同位素跟踪;

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