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红海藻对高脂肪饮食诱导肥胖小鼠的抗肥胖作用,通过抑制白色脂肪组织中成脂因子和增加棕色脂肪组织中产热因子。

Anti-Obesity Effects of a Red Seaweed, in Mice with High-Fat Diet-Induced Obesity via Suppression of Adipogenic Factors in White Adipose Tissue and Increased Thermogenic Factors in Brown Adipose Tissue.

机构信息

Department of Marine Life Science, Jeju National University, Jeju 63243, Korea.

Marine Biodiversity Institute of Korea, 75, Jangsan-ro 101-gil, Janghang-eup, Seocheon 33362, Korea.

出版信息

Nutrients. 2020 Jan 24;12(2):308. doi: 10.3390/nu12020308.

Abstract

Obesity is a serious metabolic syndrome characterized by high levels of cholesterol, lipids in the blood, and intracellular fat accumulation in adipose tissues. It is known that the suppression of adipogenic protein expression is an effective approach for the treatment of obesity, and regulates fatty acid storage and transportation in adipose tissues. The 60% ethanol extract of (GEE), a red seaweed from Jeju Island in Korea, was shown to exert anti-adipogenic activity in 3T3-L1 cells and in mice with high-fat diet (HFD)-induced obesity. GEE inhibited intracellular lipid accumulation in 3T3-L1 cells, and significantly reduced expression of adipogenic proteins. In vivo experiments indicated a significant reduction in body weight, as well as white adipose tissue (WAT) weight, including fatty liver, serum triglycerides, total cholesterol, and leptin contents. The expression of the adipogenic proteins, SREBP-1 and PPAR-γ, was significantly decreased by GEE, and the expression of the metabolic regulator protein was increased in WAT. The potential of GEE was shown in WAT, with the downregulation of PPAR-γ and C/EBP-α mRNA; in contrast, in brown adipose tissue (BAT), the thermogenic proteins were increased. Collectively, these research findings suggest the potential of GEE as an effective candidate for the treatment of obesity-related issues via functional foods or pharmaceutical agents.

摘要

肥胖是一种严重的代谢综合征,其特征是血液中胆固醇、脂质水平升高,以及脂肪组织中细胞内脂肪堆积。已知抑制脂肪生成蛋白的表达是治疗肥胖症的有效方法,可调节脂肪组织中脂肪酸的储存和运输。韩国济州岛的红海藻(GEE)的 60%乙醇提取物在 3T3-L1 细胞和高脂肪饮食(HFD)诱导的肥胖小鼠中显示出抗脂肪生成活性。GEE 抑制了 3T3-L1 细胞内的脂质积累,并显著降低了脂肪生成蛋白的表达。体内实验表明,体重以及白色脂肪组织(WAT)重量显著减轻,包括脂肪肝、血清甘油三酯、总胆固醇和瘦素含量。GEE 显著降低了脂肪生成蛋白 SREBP-1 和 PPAR-γ 的表达,同时增加了 WAT 中代谢调节剂蛋白的表达。GEE 在 WAT 中的潜力表现在下调 PPAR-γ 和 C/EBP-α mRNA;相比之下,在棕色脂肪组织(BAT)中,产热蛋白增加。总的来说,这些研究结果表明,GEE 有可能通过功能性食品或药物制剂成为治疗肥胖相关问题的有效候选药物。

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