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代谢性疾病研究中的膳食ω-3多不饱和脂肪酸:基于组学的十年洞察(2014 - 2024)

Dietary Omega-3 PUFAs in Metabolic Disease Research: A Decade of Omics-Enabled Insights (2014-2024).

作者信息

Li Jing, Lin Yang-Chi-Dung, Zuo Hua-Li, Huang Hsi-Yuan, Zhang Tao, Bai Jin-Wei, Huang Hsien-Da

机构信息

School of Medicine, The Chinese University of Hong Kong, Shenzhen 518172, China.

Warshel Institute for Computational Biology, School of Medicine, The Chinese University of Hong Kong, Shenzhen 518172, China.

出版信息

Nutrients. 2025 May 28;17(11):1836. doi: 10.3390/nu17111836.

Abstract

: The rising global prevalence of metabolic diseases (e.g., obesity, type 2 diabetes mellitus) underscores the need for effective interventions. Omega-3 polyunsaturated fatty acids (PUFAs) exhibit therapeutic potential, yet their molecular mechanisms remain unclear. This systematic review synthesizes a decade (2014-2024) of omics research to elucidate Omega-3 PUFA mechanisms in metabolic diseases and identify future directions. : A PRISMA-guided search of the Web of Science identified studies on Omega-3 PUFAs, metabolic diseases, and omics. After excluding reviews, non-English articles, and irrelevant studies, 72 articles were analyzed (16 multi-omics, 17 lipidomics, 10 transcriptomics/metabolomics/microbiomics each, and 6 proteomics). : Omics studies demonstrated that Omega-3 PUFAs, particularly EPA and DHA, improve metabolic health through interconnected mechanisms. They regulate epigenetic processes, including DNA methylation and miRNA expression, influencing genes linked to inflammation and insulin sensitivity. Omega-3 PUFAs reduce oxidative stress by mitigating protein carbonylation and enhancing antioxidant defenses. Gut microbiota modulation is evident through increased beneficial taxa (e.g., Bacteroidetes, Akkermansia) and reduced pro-inflammatory species, correlating with improved metabolic parameters. Mitochondrial function is enhanced via upregulated fatty acid oxidation and TCA cycle activity, while anti-inflammatory effects arise from NF-κB pathway suppression and macrophage polarization toward an M2 phenotype. Challenges include interindividual variability in responses and a limited understanding of dynamic metabolic interactions. : Omega-3 PUFAs target multiple pathways to improve metabolic health. Future research should prioritize chemoproteomics for direct target identification, multi-omics integration, and personalized strategies combining Omega-3 with therapies like calorie restriction.

摘要

全球代谢性疾病(如肥胖症、2型糖尿病)患病率不断上升,凸显了有效干预措施的必要性。ω-3多不饱和脂肪酸(PUFAs)具有治疗潜力,但其分子机制仍不清楚。本系统综述综合了十年(2014 - 2024年)的组学研究,以阐明ω-3多不饱和脂肪酸在代谢性疾病中的作用机制,并确定未来的研究方向。:按照PRISMA指南在科学网进行搜索,确定了关于ω-3多不饱和脂肪酸、代谢性疾病和组学的研究。在排除综述、非英文文章和无关研究后,对72篇文章进行了分析(16篇多组学、17篇脂质组学、各10篇转录组学/代谢组学/微生物组学以及6篇蛋白质组学)。:组学研究表明,ω-3多不饱和脂肪酸,尤其是二十碳五烯酸(EPA)和二十二碳六烯酸(DHA),通过相互关联的机制改善代谢健康。它们调节表观遗传过程,包括DNA甲基化和微小RNA(miRNA)表达,影响与炎症和胰岛素敏感性相关的基因。ω-3多不饱和脂肪酸通过减轻蛋白质羰基化和增强抗氧化防御来降低氧化应激。肠道微生物群的调节表现为有益菌属(如拟杆菌属、阿克曼氏菌)增加,促炎菌减少,这与改善的代谢参数相关。通过上调脂肪酸氧化和三羧酸循环(TCA)活性增强线粒体功能,同时通过抑制核因子κB(NF-κB)途径和使巨噬细胞向M2表型极化产生抗炎作用。挑战包括个体反应的变异性以及对动态代谢相互作用的了解有限。:ω-3多不饱和脂肪酸靶向多种途径来改善代谢健康。未来的研究应优先进行化学蛋白质组学以直接鉴定靶点、进行多组学整合以及将ω-3与热量限制等疗法相结合的个性化策略。

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