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青蒿琥酯通过降低C/EBP-α、PPAR-γ、FAS、脂滴包被蛋白A和STAT-3的表达及/或磷酸化水平来抑制3T3-L1前脂肪细胞的脂肪生成。

Artesunate inhibits adipogeneis in 3T3-L1 preadipocytes by reducing the expression and/or phosphorylation levels of C/EBP-α, PPAR-γ, FAS, perilipin A, and STAT-3.

作者信息

Jang Byeong-Churl

机构信息

Department of Molecular Medicine, College of Medicine, Keimyung University, 1095 Dalgubeoldaero, Dalseo-gu, Daegu, 42601, South Korea.

出版信息

Biochem Biophys Res Commun. 2016 May 20;474(1):220-225. doi: 10.1016/j.bbrc.2016.04.109. Epub 2016 Apr 22.

Abstract

Differentiation of preadipocyte, also called adipogenesis, leads to the phenotype of mature adipocyte. However, excessive adipogenesis is closely linked to the development of obesity. Artesunate, one of artemisinin-type sesquiterpene lactones from Artemisia annua L., is known for anti-malarial and anti-cancerous activities. In this study, we investigated the effect of artesunate on adipogenesis in 3T3-L1 preadipocytes. Artesunate strongly inhibited lipid accumulation and triglyceride (TG) synthesis during the differentiation of 3T3-L1 preadipocytes into adipocytes at 5 μM concentration. Artesunate at 5 μM also reduced not only the expressions of CCAAT/enhancer-binding protein-α (C/EBP-α), peroxisome proliferator-activated receptor-γ (PPAR-γ), fatty acid synthase (FAS), and perilipin A but also the phosphorylation levels of signal transducer and activator of transcription-3 (STAT-3) during adipocyte differentiation. Moreover, artesunate at 5 μM reduced leptin, but not adiponectin, mRNA expression during adipocyte differentiation. Taken together, these findings demonstrate that artesunate inhibits adipogenesis in 3T3-L1 preadipoytes through the reduced expression and/or phosphorylation levels of C/EBP-α, PPAR-γ, FAS, perilipin A, and STAT-3.

摘要

前脂肪细胞的分化,也称为脂肪生成,会导致成熟脂肪细胞的表型。然而,过度的脂肪生成与肥胖的发展密切相关。青蒿琥酯是青蒿中的一种青蒿素型倍半萜内酯,以其抗疟疾和抗癌活性而闻名。在本研究中,我们研究了青蒿琥酯对3T3-L1前脂肪细胞脂肪生成的影响。在3T3-L1前脂肪细胞分化为脂肪细胞的过程中,5μM浓度的青蒿琥酯强烈抑制脂质积累和甘油三酯(TG)合成。5μM的青蒿琥酯不仅降低了CCAAT/增强子结合蛋白-α(C/EBP-α)、过氧化物酶体增殖物激活受体-γ(PPAR-γ)、脂肪酸合酶(FAS)和脂滴包被蛋白A的表达,还降低了脂肪细胞分化过程中信号转导和转录激活因子-3(STAT-3)的磷酸化水平。此外,5μM的青蒿琥酯在脂肪细胞分化过程中降低了瘦素的mRNA表达,但未降低脂联素的mRNA表达。综上所述,这些发现表明青蒿琥酯通过降低C/EBP-α、PPAR-γ、FAS、脂滴包被蛋白A和STAT-3的表达和/或磷酸化水平来抑制3T3-L1前脂肪细胞的脂肪生成。

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