首页> 美国卫生研究院文献>Nutrients >Phyllodulcin a Natural Sweetener Regulates Obesity-Related Metabolic Changes and Fat Browning-Related Genes of Subcutaneous White Adipose Tissue in High-Fat Diet-Induced Obese Mice
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Phyllodulcin a Natural Sweetener Regulates Obesity-Related Metabolic Changes and Fat Browning-Related Genes of Subcutaneous White Adipose Tissue in High-Fat Diet-Induced Obese Mice

机译:天然甜味剂Phyllodulcin调节高脂饮食诱导的肥胖小鼠的肥胖相关的代谢变化和皮下脂肪组织的褐变相关基因

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摘要

Phyllodulcin is a natural sweetener found in Hydrangea macrophylla var. thunbergii. This study investigated whether phyllodulcin could improve metabolic abnormalities in high-fat diet (HFD)-induced obese mice. Animals were fed a 60% HFD for 6 weeks to induce obesity, followed by 7 weeks of supplementation with phyllodulcin (20 or 40 mg/kg body weight (b.w.)/day). Stevioside (40 mg/kg b.w./day) was used as a positive control. Phyllodulcin supplementation reduced subcutaneous fat mass, levels of plasma lipids, triglycerides, total cholesterol, and low-density lipoprotein cholesterol and improved the levels of leptin, adiponectin, and fasting blood glucose. In subcutaneous fat tissues, supplementation with stevioside or phyllodulcin significantly decreased mRNA expression of lipogenesis-related genes, including CCAAT/enhancer-binding protein α (C/EBPα), peroxisome proliferator activated receptor γ (PPARγ), and sterol regulatory element-binding protein-1C (SREBP-1c) compared to the high-fat group. Phyllodulcin supplementation significantly increased the expression of fat browning-related genes, including PR domain containing 16 (Prdm16), uncoupling protein 1 (UCP1), and peroxisome proliferator-activated receptor γ coactivator 1-α (PGC-1α), compared to the high-fat group. Hypothalamic brain-derived neurotrophic factor-tropomyosin receptor kinase B (BDNF-TrkB) signaling was upregulated by phyllodulcin supplementation. In conclusion, phyllodulcin is a potential sweetener that could be used to combat obesity by regulating levels of leptin, fat browning-related genes, and hypothalamic BDNF-TrkB signaling.
机译:毛竹素是在绣球花中发现的天然甜味剂。黑山这项研究调查了叶绿素是否可以改善高脂饮食(HFD)诱导的肥胖小鼠的代谢异常。给动物喂食60%HFD,持续6周以诱导肥胖,然后再补充叶绿素(20或40 mg / kg体重(体重)/天),持续7周。甜菊糖(40 mg / kg b.w./天)用作阳性对照。补充叶绿素减少了皮下脂肪量,血浆脂质,甘油三酸酯,总胆固醇和低密度脂蛋白胆固醇水平,并改善了瘦素,脂联素和空腹血糖水平。在皮下脂肪组织中,补充甜菊糖苷或叶绿素可显着降低脂肪生成相关基因的mRNA表达,包括CCAAT /增强子结合蛋白α(C /EBPα),过氧化物酶体增殖物激活受体γ(PPARγ)和固醇调节元素结合蛋白-1C(SREBP-1c)与高脂组相比。相比于高剂量的大豆球藻霉素补充剂,脂肪褐变相关基因的表达显着增加,包括PR结构域包含16(Prdm16),解偶联蛋白1(UCP1)和过氧化物酶体增殖物激活受体γ共激活物1-α(PGC-1α)。 -胖组。下叶丘脑源性神经营养因子-原肌球蛋白受体激酶B(BDNF-TrkB)信号通过叶绿素补充而上调。总之,叶绿素是一种潜在的甜味剂,可通过调节瘦素,脂肪褐变相关基因和下丘脑BDNF-TrkB信号传导水平来对抗肥胖。

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