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The Combination of Resveratrol and Quercetin Attenuates Metabolic Syndrome in Rats by Modifying the Serum Fatty Acid Composition and by Upregulating SIRT 1 and SIRT 2 Expression in White Adipose Tissue

机译:白藜芦醇和槲皮素的组合通过改变血清脂肪酸组成并上调白色脂肪组织中SIRT 1和SIRT 2的表达来减轻大鼠的代谢综合征。

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摘要

Resveratrol (RSV) and quercetin (QRC) modify energy metabolism and reduce cardiovascular risk factors included in the metabolic syndrome (MetS). These natural compounds upregulate and activate sirtuins (SIRTs), a family of NAD-dependent histone deacetylases. We analyzed the effect of two doses of a commercial combination of RSV and QRC on serum fatty acid composition and their regulation of SIRTs 1–3 and PPAR-γ expression in white adipose tissue. MetS was induced in Wistar rats by adding 30% sucrose to drinking water for five months. Rats were divided into control and two groups receiving the two different doses of RSV and QRC in drinking water daily for 4 weeks following the 5 months of sucrose treatment. Commercial kits were used to determine serum parameters and the expressions of SIRTs in WAT were analysed by western blot. In MetS rats body mass, central adiposity, insulin, triglycerides, non-HDL-C, leptin, adiponectin, monounsaturated fatty acids (MUFAs), and nonesterified fatty acids (NEFAs) were increased, while polyunsaturated fatty acids (PUFAs) and HDL-C were decreased. SIRT 1 and SIRT 2 were downregulated, while PPAR-γ was increased. RSV + QRC administration improved the serum health parameters modified by MetS and upregulate SIRT 1 and SIRT 2 expression in white abdominal tissue in MetS animals.
机译:白藜芦醇(RSV)和槲皮素(QRC)可以改善能量代谢,并降低代谢综合征(MetS)中包含的心血管危险因素。这些天然化合物上调并激活sirtuins(SIRT),这是NAD依赖性组蛋白去乙酰化酶的一个家族。我们分析了两剂商业化RSV和QRC组合对白色脂肪组织中血清脂肪酸组成及其对SIRT 1–3和PPAR-γ表达的调节作用。通过在饮用水中添加30%的蔗糖达五个月,在Wistar大鼠中诱发MetS。在将蔗糖治疗5个月后,将大鼠分为对照组和两组,分别在饮用水中接受两种不同剂量的RSV和QRC,持续4周。使用商业试剂盒确定血清参数,并通过western blot分析WAT中SIRT的表达。在MetS大鼠中,体重,中枢脂肪,胰岛素,甘油三酸酯,非HDL-C,瘦素,脂联素,单不饱和脂肪酸(MUFA)和非酯化脂肪酸(NEFA)增加,而多不饱和脂肪酸(PUFA)和HDL- C降低。 SIRT 1和SIRT 2下调,而PPAR-γ增加。 RSV + QRC给药改善了由MetS修饰的血清健康参数,并上调了MetS动物白色腹部组织中SIRT 1和SIRT 2的表达。

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