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N-Acetylneuraminic Acid Supplementation Prevents High Fat Diet-Induced Insulin Resistance in Rats through Transcriptional and Nontranscriptional Mechanisms

机译:补充N-乙酰神经氨酸通过转录和非转录机制预防高脂饮食诱导的大鼠胰岛素抵抗

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摘要

N-Acetylneuraminic acid (Neu5Ac) is a biomarker of cardiometabolic diseases. In the present study, we tested the hypothesis that dietary Neu5Ac may improve cardiometabolic indices. A high fat diet (HFD) + Neu5Ac (50 or 400 mg/kg BW/day) was fed to rats and compared with HFD + simvastatin (10 mg/kg BW/day) or HFD alone for 12 weeks. Weights and serum biochemicals (lipid profile, oral glucose tolerance test, leptin, adiponectin, and insulin) were measured, and mRNA levels of insulin signaling genes were determined. The results indicated that low and high doses of sialic acid (SA) improved metabolic indices, although only the oral glucose tolerance test, serum triglycerides, leptin, and adiponectin were significantly better than those in the HFD and HFD + simvastatin groups (P < 0.05). Furthermore, the results showed that only high-dose SA significantly affected the transcription of hepatic and adipose tissue insulin signaling genes. The data suggested that SA prevented HFD-induced insulin resistance in rats after 12 weeks of administration through nontranscriptionally mediated biochemical changes that may have differentially sialylated glycoprotein structures at a low dose. At higher doses, SA induced transcriptional regulation of insulin signaling genes. These effects suggest that low and high doses of SA may produce similar metabolic outcomes in relation to insulin sensitivity through multiple mechanisms. These findings are worth studying further.
机译:N-乙酰神经氨酸(Neu5Ac)是心脏代谢疾病的生物标志物。在本研究中,我们测试了饮食中Neu5Ac可以改善心脏代谢指数的假设。将高脂饮食(HFD)+ Neu5Ac(50或400μg/ kg BW /天)喂给大鼠,并与HFD +辛伐他汀(10μmg/ kg BW /天)或单独的HFD比较12周。测量体重和血清生化试剂(脂质谱,口服葡萄糖耐量试验,瘦素,脂联素和胰岛素),并测定胰岛素信号基因的mRNA水平。结果表明,低和高剂量的唾液酸(SA)改善了代谢指标,尽管仅口服葡萄糖耐量试验,血清甘油三酯,瘦素和脂联素明显优于HFD和HFD +辛伐他汀组(P <0.05 )。此外,结果表明,只有高剂量的SA才能显着影响肝和脂肪组织胰岛素信号转导基因的转录。数据表明,给药后12周,SA通过非转录介导的生化变化(可能具有低剂量的唾液酸化糖蛋白结构差异)阻止了HFD诱导的大鼠胰岛素抵抗。在较高剂量下,SA诱导胰岛素信号基因的转录调控。这些效应表明,低剂量和高剂量的SA可能通过多种机制产生与胰岛素敏感性相关的相似代谢结果。这些发现值得进一步研究。

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