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首页> 外文期刊>Journal of biochemical and molecular toxicology >Improvement of insulin resistance via increase of GLUT4 and PPARγ in metabolic syndrome‐induced rats treated with omega‐3 fatty acid or l l ‐carnitine
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Improvement of insulin resistance via increase of GLUT4 and PPARγ in metabolic syndrome‐induced rats treated with omega‐3 fatty acid or l l ‐carnitine

机译:通过ω-3脂肪酸或L L L-Carnitine的代谢综合征诱导大鼠Glut4和PPARγ增加通过Glut4和PPARγ增加改善胰岛素抵抗

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Abstract Background Frequent consumption of fructose and saturated fatty acids increase risk of metabolic syndrome (MS). Features of MS include insulin resistance, dyslipidemia, visceral obesity, and hypertension. The aim of this study was to investigate the role of omega‐3 and l ‐carnitine in ameliorating features of MS. Methods MS was induced in rats by high‐fructose high‐fat fed diet for 8 weeks. They were randomly divided into five groups: normal control, MS control group treated with saline, MS groups given omega‐3 (260?mg/kg), l ‐carnitine (200?mg/kg), or metformin (100?mg/kg) daily for 4 weeks. Body weight, relative organ weight, glucose, insulin, adiponectin, and lipid profiles were estimated. Also glucose transporter 4 (GLUT4) content and peroxisome proliferator‐activated receptor‐gamma (PPARγ) protein expressions were determined. Results Omega‐3 and l ‐carnitine caused decrease in both MS‐induced increase in body weight and glucose similar to metformin. They reduced insulin level and resistance with increased adiponectin, and correction of MS‐induced hyperlipidemia. Drugs also increased GLUT4 and PPARγ protein expression compared with MS control group. Conclusion Omega‐3 and l ‐carnitine improve features of MS via increased GLUT4 and PPARγ expression.
机译:摘要背景常见消耗果糖和饱和脂肪酸增加了代谢综合征的风险(MS)。 MS的特征包括胰岛素抵抗,血脂血症,内脏肥胖和高血压。本研究的目的是探讨Omega-3和L-Carnitine在MS的改善特征中的作用。方法通过高果糖高喂养饮食诱导MS在大鼠中诱导8周。将它们随机分为五组:正常对照,用盐水处理的MS对照组,MS组给定OMEGA-3(260?Mg / kg),L-碱(200〜Mg / kg)或二甲双胍(100?mg / kg)每天4周。估计体重,相对器官重量,葡萄糖,胰岛素,脂联素和脂质型材。还确定葡萄糖转运蛋白4(Glut4)含量和过氧化物体增殖物激活的受体-γ(PPARγ)蛋白表达。结果Omega-3和L-碱引起的MS诱导的体重增加和葡萄糖的增加降低,类似于二甲双胍。它们降低了胰岛素水平和抗性增加的脂肪切除型,以及MS诱导的高脂血症的校正。与MS对照组相比,药物也增加了Glut4和PPARγ蛋白表达。结论Omega-3和L-Carnitine通过增加的Glut4和PPARγ表达改善MS的特征。

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