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Qing Gan Zi Shen Tang alleviates adipose tissue dysfunction with up-regulation of SIRT1 in spontaneously hypertensive rat

机译:清甘子沉唐减轻了脂肪组织功能障碍在自发性高血压大鼠中升压SIRT1

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Qing Gan Zi Shen Tang (QGZST) is a famous traditional Chinese medicine formula in the Jiangsu Province Hospital of Traditional Chinese Medicine for its efficacy in treating hypertension, obesity, hyperlipidemia and insulin resistance. The current study further evaluated the effects and possible mechanisms of QGZST on epididymal white adipose tissue (eWAT) dysfunction in a high-fat-diet (HFD)-fed-spontaneously hypertensive rat (SHR) model. Results showed that QGZST significantly decreased the systolic blood pressure (SBP), mean arterial blood pressure (MAP), body weights and adipocyte size of HFD-fed SHRs. Moreover, QGZST remarkably reduced the serum levels of cholesterol, triglyceride, low-density lipoprotein cholesterol, fasting glucose, fasting insulin and HOMA-IR index, increased serum high-density lipoprotein cholesterol levels and improved glucose intolerance in HFD-fed SHRs. Furthermore, QGZST dramatically attenuated HFD-fed-induced hypersecretion of proinflammatory cytokines and hypoproduction of adiponectin in SHRs. Mechanistically, QGZST stimulated the activity of Sirtuin 1 (SIRT1) and Forkhead box protein 01 (FOXO1) and suppress the expression of peroxisome proliferator-activated receptor-gamma (PPAR-gamma), CCAAT-enhancer-binding proteins-alpha(C/EBP-alpha), fatty acid binding protein 4 (FABP4), acetylated nuclear factor-kappa-B-p65 (acetyl-NF-kappa B-p65) and protein-tyrosine phosphatase 1B (PTP1B). More than that, QGZST also prevented acetyl-NF-kappa B-p65 nuclear accumulation. Collectively, our research demonstrated for the first time that QGZST is able to alleviate eWAT dysfunction with up-regulation of SIRT1 in HFD-fed SHRs, which might supply further insight into QGZST-mediated anti-hypertension and antiobesity effects.
机译:清甘子沉堂(QGZST)是江苏省中药公式的中医院,中医院治疗高血压,肥胖,高脂血症和胰岛素抵抗的疗效。目前的研究进一步评估了QGZST在高脂饮食(HFD)-Fed-自发性高血压大鼠(SHR)模型中对附睾白色脂肪组织(EWAT)功能障碍的影响和可能机制。结果表明,QGZST显着降低了收缩压(SBP),平均动脉血压(MAP),体重和脂肪细胞大小的HFD喂养SHR。此外,QGZST显着降低了血清胆固醇,甘油三酯,低密度脂蛋白胆固醇,空腹葡萄糖,禁食胰岛素和HOMA-IR指数,增加了血清高密度脂蛋白胆固醇水平,并改善了HFD喂养的SHR中的葡萄糖不耐受。此外,QGZST显着衰减了促炎细胞因子的HFD喂养诱导的过度折叠,并在SHR中的脂联素的钙切除蛋白酶。机械地,QGZST刺激了SIRTUIN 1(SIRT1)和FORKHEAD箱蛋白01(FOXO1)的活性,并抑制过氧化物体增殖物激活的受体-γ(PPAR-GAMMA),CCAAT-增强子结合蛋白-α的表达(C / EBP) - 乳酸),脂肪酸结合蛋白4(FABP4),乙酰化核因子-Kappa-B-P65(乙酰-NF-κB-P65)和蛋白质 - 酪氨酸磷酸酶1B(PTP1B)。 qgzst还预防乙酰-nf-κB-p65核积累。统称,我们的研究首次展示了QGZST能够缓解eWAT功能障碍在HFD喂养SHR中升高SIRT1,这可能会进一步了解QGZST介导的抗高血压和抗病性效应。

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