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大豆叶通过调节饮食诱导肥胖小鼠和3T3-L1脂肪细胞中脂肪生成转录因子及脂肪氧化发挥抗肥胖作用

Anti-Obesity Effects of Soy Leaf via Regulation of Adipogenic Transcription Factors and Fat Oxidation in Diet-Induced Obese Mice and 3T3-L1 Adipocytes.

作者信息

Li Hua, Kang Ji-Hyun, Han Jong-Min, Cho Moon-Hee, Chung Young-Jin, Park Ki Hun, Shin Dong-Ha, Park Ho-Yong, Choi Myung-Sook, Jeong Tae-Sook

机构信息

1 National Research Laboratory of Lipid Metabolism and Atherosclerosis, Korea Research Institute of Bioscience and Biotechnology (KRIBB) , Daejeon, Korea.

2 Department of Biomolecular Science, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Korea University of Science and Technology , Daejeon, Korea.

出版信息

J Med Food. 2015 Aug;18(8):899-908. doi: 10.1089/jmf.2014.3388. Epub 2015 Mar 31.

Abstract

The anti-obesity effects of extracts from soy leaves (SLE) cultivated for 8 weeks (8W) or 16 weeks (16W) were investigated in diet-induced obese mice. The effects of kaempferol, an aglycone of the kaempferol glycosides that are the major component of 8W-SLE, and coumestrol, the major component of 16W-SLE, were also investigated in 3T3-L1 adipocytes. Eight-week-old male C57BL/6J mice were randomly divided into normal diet, high-fat diet (HFD), 8W-SLE (HFD+8W-SLE 50 mg kg(-1) day(-1)), 16W-SLE (HFD+16W-SLE 50 mg kg(-1) day(-1)), and Garcinia cambogia extracts (GE) (HFD+GE 50 mg kg(-1) day(-1)) groups. Body weight gain and fat accumulation of white adipose tissue (WAT) were highly suppressed by daily oral administration of 8W-SLE and 16W-SLE for 10 weeks. Supplementing a HFD with 8W-SLE and 16W-SLE regulated the mRNA expression of peroxisome proliferator-activated receptor gamma (PPARγ), CCAAT/enhancer-binding protein alpha (c/EBPα), sterol regulatory element-binding protein-1 (SREBP-1), adipocyte protein 2, and fatty acid synthase (FAS), which are related to adipogenesis, in addition to hormone-sensitive lipase (HSL), carnitine palmitoyl transferase 1 (CPT-1), and uncoupling protein 2 (UCP2), which are related to fat oxidation in WAT. In 3T3-L1 adipocytes, kaempferol and coumestrol exhibited anti-adipogenic effects via downregulation of PPARγ, c/EBPα, SREBP-1, and FAS. Kaempferol and coumestrol increased the expression of HSL, CPT-1, and UCP2.

摘要

在饮食诱导的肥胖小鼠中研究了培养8周(8W)或16周(16W)的大豆叶提取物(SLE)的抗肥胖作用。还在3T3-L1脂肪细胞中研究了山奈酚(8W-SLE的主要成分山奈酚糖苷的苷元)和香豆雌酚(16W-SLE的主要成分)的作用。将8周龄雄性C57BL / 6J小鼠随机分为正常饮食、高脂饮食(HFD)、8W-SLE(HFD + 8W-SLE 50 mg kg⁻¹ 天⁻¹)、16W-SLE(HFD + 16W-SLE 50 mg kg⁻¹ 天⁻¹)和藤黄果提取物(GE)(HFD + GE 50 mg kg⁻¹ 天⁻¹)组。每天口服8W-SLE和16W-SLE 10周可高度抑制体重增加和白色脂肪组织(WAT)的脂肪积累。用8W-SLE和16W-SLE补充高脂饮食除了调节与WAT中脂肪氧化相关的激素敏感性脂肪酶(HSL)、肉碱棕榈酰转移酶1(CPT-1)和解偶联蛋白2(UCP2)外,还调节了与脂肪生成相关的过氧化物酶体增殖物激活受体γ(PPARγ)、CCAAT/增强子结合蛋白α(c/EBPα)、固醇调节元件结合蛋白-1(SREBP-1)、脂肪细胞蛋白2和脂肪酸合酶(FAS)的mRNA表达。在3T3-L1脂肪细胞中,山奈酚和香豆雌酚通过下调PPARγ、c/EBPα、SREBP-1和FAS表现出抗脂肪生成作用。山奈酚和香豆雌酚增加了HSL、CPT-1和UCP2的表达。

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