Fish Oil Supplementation Mitigates High-Fat Diet-Induced Obesity: Exploring Epigenetic Modulation and Genes Associated with Adipose Tissue Dysfunction in Mice

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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Abstract

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.
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
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。
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