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N3-PUFA 调控白色脂肪组织内分泌功能的机制。

Mechanisms underlying N3-PUFA regulation of white adipose tissue endocrine function.

机构信息

Department of Human Health and Nutritional Sciences, University of Guelph, Guelph, Ontario N1G 2W1, Canada.

Department of Human Health and Nutritional Sciences, University of Guelph, Guelph, Ontario N1G 2W1, Canada.

出版信息

Curr Opin Pharmacol. 2020 Jun;52:40-46. doi: 10.1016/j.coph.2020.04.009. Epub 2020 Jun 5.

Abstract

Omega-3 polyunsaturated fatty acids (N3-PUFA) are widely reported to improve obesity-associated metabolic impairments, in part, through the regulation of adipokine and cytokine secretion from white adipose tissue (WAT). However, the precise underlying molecular mechanisms by which N3-PUFA influence WAT endocrine function remain poorly described. Available evidence supports that N3-PUFA and related bioactive lipid mediators regulate several intracellular pathways that converge on two important transcription factors: PPAR-γ and NF-κB. Further, N3-PUFA signaling through GPR120 appears integral for the regulation of adipokine and cytokine production. This review collates insights from in vitro and in vivo studies using genetic and chemical inhibition of key signaling proteins to describe the pathways by which N3-PUFA regulate WAT endocrine function. Existing gaps in knowledge and opportunities to advance our understanding in this area are also highlighted.

摘要

ω-3 多不饱和脂肪酸(N3-PUFA)被广泛报道可改善与肥胖相关的代谢损伤,部分原因是通过调节白色脂肪组织(WAT)中的脂肪因子和细胞因子的分泌。然而,N3-PUFA 影响 WAT 内分泌功能的确切潜在分子机制仍描述不清。现有证据表明,N3-PUFA 和相关生物活性脂质介质调节几个细胞内途径,这些途径集中在两个重要的转录因子上:PPAR-γ 和 NF-κB。此外,GPR120 介导的 N3-PUFA 信号传导对于调节脂肪因子和细胞因子的产生是必不可少的。本综述汇集了使用遗传和化学抑制关键信号蛋白的体外和体内研究的见解,以描述 N3-PUFA 调节 WAT 内分泌功能的途径。还强调了该领域现有知识空白和进一步深入理解的机会。

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