补充鱼油可减轻高脂饮食诱发的肥胖:探索小鼠表观遗传调控和与脂肪组织功能障碍相关的基因

Pharmaceuticals Pub Date : 2024-07-01 DOI:10.3390/ph17070861
Jussara de Jesus Simão, Andressa de Sousa Bispo, V. Plata, Lucia Armelin-Correa, M. I. Alonso-Vale
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摘要

本研究调查了鱼油(FO)(尤其是富含二十碳五烯酸(EPA)的鱼油)处理对高脂饮食(HFD)诱导的小鼠肥胖症的影响。研究重点是阐明鱼油对白色脂肪组织(WAT)表观遗传修饰的影响以及脂肪衍生干细胞(ASCs)的参与。将C57BL/6j小鼠分为两组:对照组和高密度脂蛋白饮食组,连续16周。在最后8周,HFD组又分为HFD和HFD + FO(用FO处理)两组。移除脂肪以提取 RNA 和蛋白质,同时分离、培养 ASCs 并用瘦素处理。所有样本都使用功能基因组学工具进行了分析,包括 PCR 阵列、RT-PCR 和 Western 印迹分析。接受高密度脂蛋白膳食的小鼠显示出体重增加、脂肪积累以及与WAT炎症和功能障碍相关的基因表达改变。补充 FO 可减轻这些影响,从而对 HFD 引起的肥胖起到潜在的保护作用。对H3K27的分析表明,HFD诱导了组蛋白的变化,而FO治疗可部分逆转这种变化。这项研究进一步探讨了ASCs中的瘦素信号转导,提出了在WAT富含肥胖瘦素的环境中ASC功能障碍的潜在机制。总之,补充 FO 能有效缓解 HFD 诱导的肥胖,影响表观遗传和分子通路,并揭示 ASCs 和瘦素信号在肥胖相关的 WAT 功能障碍中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fish Oil Supplementation Mitigates High-Fat Diet-Induced Obesity: Exploring Epigenetic Modulation and Genes Associated with Adipose Tissue Dysfunction in Mice
This study investigated the effects of fish oil (FO) treatment, particularly enriched with eicosapentaenoic acid (EPA), on obesity induced by a high-fat diet (HFD) in mice. The investigation focused on elucidating the impact of FO on epigenetic modifications in white adipose tissue (WAT) and the involvement of adipose-derived stem cells (ASCs). C57BL/6j mice were divided into two groups: control diet and HFD for 16 weeks. In the last 8 weeks, the HFD group was subdivided into HFD and HFD + FO (treated with FO). WAT was removed for RNA and protein extraction, while ASCs were isolated, cultured, and treated with leptin. All samples were analyzed using functional genomics tools, including PCR-array, RT-PCR, and Western Blot assays. Mice receiving an HFD displayed increased body mass, fat accumulation, and altered gene expression associated with WAT inflammation and dysfunction. FO supplementation attenuated these effects, a potential protective role against HFD-induced obesity. Analysis of H3K27 revealed HFD-induced changes in histone, which were partially reversed by FO treatment. This study further explored leptin signaling in ASCs, suggesting a potential mechanism for ASC dysfunction in the obesity-rich leptin environment of WAT. Overall, FO supplementation demonstrated efficacy in mitigating HFD-induced obesity, influencing epigenetic and molecular pathways, and shedding light on the role of ASCs and leptin signaling in WAT dysfunction associated with obesity.
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