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表曲菌素通过 Wnt/β-连环蛋白通路减轻脂肪生成早期阶段,并抑制高脂肪饮食诱导的小鼠肥胖。

Ascochlorin Attenuates the Early Stage of Adipogenesis via the Wnt/β-Catenin Pathway and Inhibits High-Fat-Diet-Induced Obesity in Mice.

机构信息

Research Institute of Biomedical Engineering and Department of Cell Biology, Daegu Catholic University School of Medicine, Daegu 42472, Republic of Korea.

Department of Internal Medicine, Daegu Catholic University School of Medicine, Daegu 42472, Republic of Korea.

出版信息

Int J Mol Sci. 2024 Sep 23;25(18):10226. doi: 10.3390/ijms251810226.

Abstract

This study investigated the effects of ascochlorin (ASC), a natural compound derived from the fungus , on adipogenesis and obesity. We determined the effects of ASC on 3T3-L1 preadipocytes and whether it ameliorated to mitigate high-fat diet (HFD)-induced obesity in C57BL/6J mice. We found that ASC significantly inhibited the differentiation of preadipocytes by modulating the Wnt/β-catenin signaling pathway, a key regulator of adipogenic processes. Treatment with ASC not only reduced the mRNA and protein expression of key adipogenic transcription factors such as C/EBPα and PPARγ, but also reduced lipid accumulation both in vitro and in vivo. In addition, treatment HFD-fed mice with ASC significantly reduced their weight gain and adiposity vs. control mice. These results suggest that ASC has considerable potential as a therapeutic agent for obesity, owing to its dual action of inhibiting adipocyte differentiation and reducing lipid accumulation. Thus, ASC represents a promising candidate as a natural anti-obesity agent.

摘要

本研究探讨了来源于真菌的天然化合物 ascochlorin(ASC)对脂肪生成和肥胖的影响。我们确定了 ASC 对 3T3-L1 前脂肪细胞的影响,以及它是否能改善高脂肪饮食(HFD)诱导的 C57BL/6J 小鼠肥胖。我们发现 ASC 通过调节 Wnt/β-catenin 信号通路显著抑制前脂肪细胞的分化,该通路是脂肪生成过程的关键调节剂。ASC 的治疗不仅降低了关键脂肪生成转录因子如 C/EBPα 和 PPARγ 的 mRNA 和蛋白表达,而且还减少了体外和体内的脂质积累。此外,用 ASC 治疗 HFD 喂养的小鼠可显著减轻其体重增加和肥胖程度。这些结果表明,ASC 具有作为肥胖治疗剂的巨大潜力,因为其抑制脂肪细胞分化和减少脂质积累的双重作用。因此,ASC 作为一种天然的抗肥胖剂具有很大的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d970/11432539/8d6dd1d87942/ijms-25-10226-g001.jpg

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