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ω-3 脂肪酸可减少胰岛素抵抗患者脂肪组织中的巨噬细胞。

Omega-3 fatty acids reduce adipose tissue macrophages in human subjects with insulin resistance.

机构信息

Department of Medicine, Division of Endocrinology, and Barnstable Brown Diabetes and Obesity Center, University of Kentucky, Lexington, Kentucky, USA.

出版信息

Diabetes. 2013 May;62(5):1709-17. doi: 10.2337/db12-1042. Epub 2013 Jan 17.

Abstract

Fish oils (FOs) have anti-inflammatory effects and lower serum triglycerides. This study examined adipose and muscle inflammatory markers after treatment of humans with FOs and measured the effects of ω-3 fatty acids on adipocytes and macrophages in vitro. Insulin-resistant, nondiabetic subjects were treated with Omega-3-Acid Ethyl Esters (4 g/day) or placebo for 12 weeks. Plasma macrophage chemoattractant protein 1 (MCP-1) levels were reduced by FO, but the levels of other cytokines were unchanged. The adipose (but not muscle) of FO-treated subjects demonstrated a decrease in macrophages, a decrease in MCP-1, and an increase in capillaries, and subjects with the most macrophages demonstrated the greatest response to treatment. Adipose and muscle ω-3 fatty acid content increased after treatment; however, there was no change in insulin sensitivity or adiponectin. In vitro, M1-polarized macrophages expressed high levels of MCP-1. The addition of ω-3 fatty acids reduced MCP-1 expression with no effect on TNF-α. In addition, ω-3 fatty acids suppressed the upregulation of adipocyte MCP-1 that occurred when adipocytes were cocultured with macrophages. Thus, FO reduced adipose macrophages, increased capillaries, and reduced MCP-1 expression in insulin-resistant humans and in macrophages and adipocytes in vitro; however, there was no measureable effect on insulin sensitivity.

摘要

鱼油(FOs)具有抗炎作用,并能降低血清甘油三酯。本研究观察了 FO 治疗人类后脂肪组织和肌肉的炎症标志物,并测量了 ω-3 脂肪酸对体外脂肪细胞和巨噬细胞的影响。胰岛素抵抗的非糖尿病患者接受 ω-3 酸乙酯(4 克/天)或安慰剂治疗 12 周。FO 降低了血浆巨噬细胞趋化蛋白 1(MCP-1)水平,但其他细胞因子水平没有变化。FO 治疗组的脂肪组织(而非肌肉组织)巨噬细胞减少,MCP-1 减少,毛细血管增加,且巨噬细胞数量最多的患者对治疗的反应最大。治疗后,脂肪组织和肌肉组织中的 ω-3 脂肪酸含量增加;然而,胰岛素敏感性或脂联素没有变化。在体外,M1 极化的巨噬细胞表达高水平的 MCP-1。添加 ω-3 脂肪酸可降低 MCP-1 的表达,而对 TNF-α 没有影响。此外,ω-3 脂肪酸抑制了巨噬细胞与脂肪细胞共培养时脂肪细胞中 MCP-1 的上调。因此,FO 减少了胰岛素抵抗人群的脂肪组织巨噬细胞,增加了毛细血管,并降低了 MCP-1 的表达,在体外也降低了巨噬细胞和脂肪细胞中的 MCP-1 表达;然而,对胰岛素敏感性没有可测量的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90d6/3636648/f3e7e23fa39b/1709fig1.jpg

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