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首页> 外文期刊>Biological research: BR >Shenhua Tablet inhibits mesangial cell proliferation in rats with chronic anti-Thy-1 nephritis
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Shenhua Tablet inhibits mesangial cell proliferation in rats with chronic anti-Thy-1 nephritis

机译:参花片抑制慢性Thy-1肾炎大鼠系膜细胞增殖

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摘要

In China, mesangial proliferative glomerulonephritis (MsPGN) is one of the most common kidney diseases. In this study, we treated a rat model of chronic anti-Thy-1 MsPGN with Shenhua Tablet and evaluated whether the tablet was able to protect the kidney function. Thirty-six Wistar rats were randomly divided into six groups: (1) Sham surgery (Sham); (2) anti-Thy-1 nephritis model (Thy-1); (3) anti-Thy-1 nephritis model?+?irbesartan-treated (Irb); (4) anti-Thy-1 nephritis model?+?low-dose of Shenhua Tablet (SHL); (5) anti-Thy-1 nephritis model?+?medium-dose of Shenhua Tablet (SHM); (6) anti-Thy-1 nephritis model?+?high-dose of Shenhua Tablet (SHH). Thirteen weeks after drug treatment, urinary proteins were quantified and renal pathological changes were thoroughly examined at the time point of 24?h. Meanwhile, the expression levels of p-Erk1/2, cyclin D1 and p21 at the renal cortex were also tested. The levels of urinary proteins and total cholesterol in the blood were significantly reduced in rats treated with any drug tested in this study. The level of triglyceride was significantly reduced in all three Shenhua Tablet-treated groups. Renal pathomorphological scores were significantly improved in groups of Irb, SHM and SHH. Mesangial cell proliferation was significantly inhibited in any drug-treated group. p-Erk1/2 and cyclin D1 were downregulated whereas p21 was upregulated in the renal cortex. Our study indicated that Shenhua Tablet is able to inhibit the abnormal proliferation of mesangial cells and to prevent kidney damage, which is likely associated with downregulation of p-Erk1/2 and reduced activity of its downstream target-cyclin D1.
机译:在中国,肾小球膜增生性肾小球肾炎(MsPGN)是最常见的肾脏疾病之一。在这项研究中,我们用神华片治疗了慢性抗Thy-1 MsPGN大鼠模型,并评估了该片是否能够保护肾脏功能。将Wistar大鼠36只随机分为6组:(1)假手术(Sham); (2)抗Thy-1肾炎模型(Thy-1); (3)抗Thy-1肾炎模型+厄贝沙坦治疗(Irb); (4)抗Thy-1肾炎模型+小剂量神华片(SHL); (5)抗Thy-1肾炎模型+中剂量神华片(SHM); (6)抗Thy-1肾炎模型+大剂量神华片(SHH)。药物治疗后十三周,定量尿蛋白,并在24小时时彻底检查肾脏病理变化。同时,还检测了p-Erk1 / 2,细胞周期蛋白D1和p21在肾皮质的表达水平。在用本研究中测试的任何药物治疗的大鼠中,血液中尿蛋白和总胆固醇的水平均显着降低。在所有三个经神华片治疗的组中,甘油三酯水平均显着降低。 Irb,SHM和SHH组的肾脏病理形态学评分明显改善。在任何药物治疗组中,肾小球膜细胞的增殖均被显着抑制。 p-Erk1 / 2和细胞周期蛋白D1在肾皮质中下调,而p21在肾皮质中上调。我们的研究表明,神华片能够抑制肾小球系膜细胞的异常增殖并预防肾脏损害,这可能与p-Erk1 / 2的下调和下游靶细胞周期蛋白D1的活性降低有关。

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