Department of Medicine, Division of Endocrinology, and Barnstable Brown Diabetes and Obesity Center, University of Kentucky, Lexington, Kentucky, USA.
Diabetes. 2013 May;62(5):1709-17. doi: 10.2337/db12-1042. Epub 2013 Jan 17.
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.
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。