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制何首乌(Polygonum multiflorum Thunb.)乙醇提取物可抑制 3T3-L1 前体脂肪细胞分化和肥胖小鼠肥胖。

Heshouwu (Polygonum multiflorum Thunb.) ethanol extract suppresses pre-adipocytes differentiation in 3T3-L1 cells and adiposity in obese mice.

机构信息

Department of Food and Nutrition, Sunchon National University, Suncheon, 57922, Republic of Korea.

Mokpo Marin Food-Industry Research Center, Mokpo, 58621, Republic of Korea.

出版信息

Biomed Pharmacother. 2018 Oct;106:355-362. doi: 10.1016/j.biopha.2018.06.140. Epub 2018 Jul 11.

Abstract

This study investigated whether Heshouwu (Polygonum multiflorum Thunb.) root ethanol extract (PME) has anti-obesity activity using 3T3-L1 cells and high-fat diet (HFD)-induced obese mice. Treatment with PME (5 and 10 μg/mL) dose-dependently suppressed 3T3-L1 pre-adipocyte differentiation to adipocytes and cellular triglyceride contents. In addition, PME inhibited mRNA and protein expression of adipogenic transcription factors such as CCAAT/enhancer-binding protein α (C/EBPα) and peroxisome proliferator-activated receptor γ (PPARγ), which led to down-regulation of fatty acid synthase gene expression. After feeding mice PME (0.05%) with HFD for 12 weeks, their visceral fat mass, size and body weight were significantly reduced compared with the HFD group. Furthermore, PME supplementation significantly up-regulated the PPARα, CPT1, CPT2, UCP1 and HSL mRNA levels compared with the HFD group, whereas it down-regulated expression of the PPARγ and DGAT2 genes. Finally, HFD increased serum leptin, insulin, glucose and insulin and glucose levels; however, PME reversed these changes. These results demonstrated that PME might relieve obesity that occurs via inhibition of adipogenesis and lipogenesis as well as through lipolysis and fatty acid oxidation in 3T3-L1 cells and HFD-induced obese mice.

摘要

本研究旨在探讨制何首乌(Polygonum multiflorum Thunb.)根乙醇提取物(PME)对 3T3-L1 细胞和高脂饮食(HFD)诱导肥胖小鼠是否具有抗肥胖活性。PME(5 和 10μg/mL)浓度依赖性地抑制 3T3-L1 前脂肪细胞向脂肪细胞分化和细胞内甘油三酯含量。此外,PME 抑制了脂肪生成转录因子如 CCAAT/增强子结合蛋白α(C/EBPα)和过氧化物酶体增殖物激活受体γ(PPARγ)的 mRNA 和蛋白表达,导致脂肪酸合酶基因表达下调。用 HFD 喂养小鼠 PME(0.05%)12 周后,与 HFD 组相比,其内脏脂肪质量、大小和体重明显减轻。此外,与 HFD 组相比,PME 补充显著上调了 PPARα、CPT1、CPT2、UCP1 和 HSL mRNA 水平,而下调了 PPARγ和 DGAT2 基因的表达。最后,HFD 增加了血清瘦素、胰岛素、葡萄糖和胰岛素及葡萄糖水平;然而,PME 逆转了这些变化。这些结果表明,PME 可能通过抑制脂肪生成和脂肪生成,以及通过 3T3-L1 细胞和 HFD 诱导肥胖小鼠的脂肪分解和脂肪酸氧化来缓解肥胖。

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