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Saikosaponin-d Prevents the Progression of Mesangioproliferative Glomerulonephritis in Rats

机译:Saikosaponin-D可以防止大鼠中镁丙酮化肾小球肾炎的进展

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Aims: the preventive effects of Saikosaponin-d (Ssd) on the progression of mesangioproliferative glomerulonephritis, induced by intravenous infection of anti-Thyl monoclonal antibody (mAb) 1-22-3 into uninephrectomized rats, were evaluated. Methods: eighteen rats were divided into three groups of six. One group was treated with phosphate buffered saline (PBS) as a control. The other two groups were treated with Ssd 1.8 mg/kg body weight (BW)/day or 0.6 mg/kg BW/day respectively. Urine samples were collected from the rats in metabolic cages on days 1,4, 8, 14 and 21 after the injection of mAb 1-22-3. Systolic BP (SBP) was tested on days 1, 5, 10, 14 and 18 after the injection. All rats were sacrificed 21 days after the injection of mAb 1-22-3 for blood biochemistry, RNA preparation from isolated glomeruli, and immunofluorescent and light microscopy of the kidney. Results: Ssd suppressed proteinuria, extracellular matrix expansion, crescentic formation as well as inflammatory cell infiltration recognized by mAb OX8, EDI and TRPM3. Especially, Ssd was shown to have highly significant suppressive effect on CD8+ T cells infiltration into the periglomerular and tubulointerstitial areas, as shown in Table 1 and on expression of a -SMA along Bowman's capsule as shown in Figures 7E and 7F. Conclusion: Saikosapoin-d prevented the progression of mesangioproliferative glomerulonephritis in rats, which might be closely linked to the markedly significant suppressive effects of Ssd on CD8+ T cells infiltration into the periglomerular and tubulointerstitial areas, as well as on the expression of a -SMA along Bowman's capsule.
机译:目的:评价索科酮蛋白-D(SSD)对MesangioCloIferative肾小球肾炎进展的预防效果,通过静脉内感染抗叔丁基单克隆抗体(MAb)1-22-3诱导为单腋次化大鼠。方法:将十八大鼠分为六组三组。将一组用磷酸盐缓冲盐水(PBS)作为对照处理。另外两组分别用SSD 1.8mg / kg体重(BW)/天或0.6mg / kg BW /天处理。在注射mAb 1-22-3后的第1,4,8,14和21天,从代谢笼中的大鼠中收集尿液样品。在注射后的第1,5,10,14和18天测试收缩压BP(SBP)。在注射mAb 1-22-3后21天处死所有大鼠,用于血液化学,来自分离的肾小球的RNA制备,以及肾脏的免疫荧光和光学显微镜。结果:SSD抑制蛋白尿,细胞外基质膨胀,新月形的形成以及MAB OX8,EDI和TRPM3识别的炎症细胞浸润。特别地,SSD被证明对CD8 + T细胞浸润的显着抑制作用浸润到脊柱孔和微管间区域中,如表1所示和沿鲍曼胶囊的-Sma表达,如图7E和7F所示。结论:Saikosapoin-D预防大鼠中MesangioProiferativerative肾小球肾炎的进展,这可能与SSD对CD8 + T细胞浸润的显着显着的抑制作用与Periglomer和微管间区域的表达密切相关,以及-Sma的表达鲍曼的胶囊。

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