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由于亚麻籽油具有抗炎免疫调节潜力,肥胖诱导的胰岛素抵抗得到部分逆转。

Partial Reversal of Obesity-Induced Insulin Resistance Owing to Anti-Inflammatory Immunomodulatory Potential of Flaxseed Oil.

作者信息

Bashir Samina, Ali Shakir, Khan Farah

机构信息

Department of Biochemistry, Faculty of Science, Hamdard University , New Delhi , India.

出版信息

Immunol Invest. 2015;44(5):451-69. doi: 10.3109/08820139.2015.1025960.

DOI:10.3109/08820139.2015.1025960
PMID:26107745
Abstract

The present study was designed to assess the potential of supplementation of diet with Flaxseed (Linum usitatissimum, L.) oil (FXO), on obesity-related inflammation and reversal of obesity-induced insulin resistance. Swiss Albino mice, C57bl/6 mice and co-culture of 3T3-L1 adipocytes - RAW 264.7 macrophages to mimick obese adipose tissue environment were used for the study. Oral gavage of FXO at concentrations of 4, 8 or 16 mg/kg body weight (bwt) for 4 weeks or high-fat diet (HFD, 60% energy as fat) supplemented with dietary FXO (4, 8 or 16 mg/kg bwt) was given to the mice. FXO was characterised using gas chromatography - mass spectrometry. FXO supplemented HFD-fed mice (4 mg/kg bwt exhibited reduced adiposity index, serum glucose levels and triglycerides (8 and 16 mg/kg bwt) and improvement in insulin sensitisation (4, 8 and 16 mg/kg bwt) when compared with HFD mice. The co-culture showed a dose-dependent shift in cytokines towards anti-inflammatory (IL-4) state, with a decrease in pro-inflammatory TNF-α (p < 0.05). For immunomodulatory studies a dose-dependent increase (p < 0.05) was observed in antigen-specific levels of Th2 (IL-4) cytokine, serum anti-ova IgG1 and IgE levels. Suppression in anti-ova IgG2a, IgG2b, and IgG3 and antigen-specific Th1 cytokines like TNF-α and IFN-γ significantly (p < 0.05) was observed at 16 mg/kg bwt dosage. The results indicate that FXO exhibits an anti-inflammatory immunomodulatory potential and may partially relieve symptoms of obesity-associated insulin resistance.

摘要

本研究旨在评估补充亚麻籽(Linum usitatissimum, L.)油(FXO)对饮食诱导肥胖相关炎症及肥胖诱导的胰岛素抵抗逆转的潜在作用。本研究使用了瑞士白化小鼠、C57bl/6小鼠以及3T3-L1脂肪细胞与RAW 264.7巨噬细胞的共培养体系来模拟肥胖脂肪组织环境。给小鼠口服浓度为4、8或16毫克/千克体重(bwt)的FXO,持续4周,或给予高脂饮食(HFD,60%的能量来自脂肪)并补充不同剂量(4、8或16毫克/千克体重)的膳食FXO。使用气相色谱 - 质谱联用仪对FXO进行表征。与高脂饮食组小鼠相比,补充FXO的高脂饮食喂养小鼠(4毫克/千克体重)的肥胖指数、血清葡萄糖水平和甘油三酯水平(8和16毫克/千克体重)降低,胰岛素敏感性得到改善(4、8和16毫克/千克体重)。共培养体系显示细胞因子呈剂量依赖性地向抗炎(IL-4)状态转变,促炎细胞因子TNF-α减少(p < 0.05)。在免疫调节研究中,观察到Th2(IL-4)细胞因子、血清抗卵清蛋白IgG1和IgE水平的抗原特异性水平呈剂量依赖性增加(p < 0.05)。在16毫克/千克体重剂量下,抗卵清蛋白IgG2a、IgG2b和IgG3以及抗原特异性Th1细胞因子如TNF-α和IFN-γ受到显著抑制(p < 0.05)。结果表明,FXO具有抗炎免疫调节潜力,可能部分缓解肥胖相关胰岛素抵抗的症状。

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