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首页> 外文期刊>Journal of food quality >Secoisolariciresinol Diglucoside Regulates Adipose Tissue Metabolic Disorder in Obese Mice Induced by a Western Diet
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Secoisolariciresinol Diglucoside Regulates Adipose Tissue Metabolic Disorder in Obese Mice Induced by a Western Diet

机译:Secoisolariciresinol Diglucoside调节西方饮食诱导的肥胖小鼠的脂肪组织代谢紊乱

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Secoisolariciresinol diglucoside (SDG) is the main component of flax lignans. Current studies have reported a positive effect of SDG on obesity and metabolic diseases. SDG has strong blood fat- and blood sugar-lowering, anti-inflammatory, and antioxidant effects and prevents heart disease and other chronic diseases. In this study, we explored the effects of SDG on Western diet-induced obesity and lipid metabolic disorder. Supplementing Western diet-induced obese mice with 40?mg kg 1 d 1 , SDG for 12 weeks significantly reduced body and tissue weights. Increased adiponectin levels and decreased serum leptin and resistin levels were observed in obese mice orally administered SDG. Proliferation of adipose tissue was observed by hematoxylin and eosin staining, and cell size was quantitatively analyzed. As a result, SDG inhibited the proliferation of adipose tissue. In addition, SDG suppressed the mRNA expression of lipid synthetic genes and upregulated the mRNA expression of lipolytic genes. Overall, these results indicate that SDG inhibits obesity induced by a Western diet and regulates adipose tissue metabolic disorder. These results provide a theoretical basis for further study on the regulation of obesity and lipid metabolic disorder caused by SDG.
机译:Secoisolariciresinol Diglucoside(SDG)是亚麻木质体的主要成分。目前的研究报告了SDG对肥胖和代谢疾病的积极作用。 SDG具有强血脂和血糖降低,抗炎和抗氧化效果,可防止心脏病和其他慢性疾病。在这项研究中,我们探讨了SDG对西方饮食诱导的肥胖和脂质代谢紊乱的影响。补充西方饮食诱导的肥胖小鼠,40毫克kg 1 d 1,sdg持续12周的体和组织重量。在口服SDG的肥胖小鼠中观察到增加脂联素水平和降低血清瘦素和抗蛋白水平。通过苏木精和曙红染色观察脂肪组织的增殖,并定量分析细胞尺寸。结果,SDG抑制了脂肪组织的增殖。此外,SDG抑制了脂质合成基因的mRNA表达并上调了脂肪溶解基因的mRNA表达。总体而言,这些结果表明SDG抑制西方饮食诱导的肥胖,并调节脂肪组织代谢紊乱。这些结果为进一步研究SDG引起的肥胖和脂质代谢障碍的进一步研究提供了理论依据。

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