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人参皂苷Rg1对多柔比星肾病大鼠足细胞nephrin的影响 被引量:12

Ginsenoside Rg1 increases the expression of nephrin in adriamycin-induced nephrotic rats
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摘要 目的足细胞的损伤是蛋白尿发生的主要机制,如何修复受损的足细胞已成为研究热点。文中观察人参皂苷Rg1对足细胞病变模型———多柔比星肾病模型的疗效及其对足细胞病变的影响。方法采用单次尾静脉注射盐酸多柔比星建立多柔比星肾病模型。SD大鼠分为空白对照组、模型组、人参皂苷Rg1高剂量组和低剂量组,分别在注射后第7、14、28天收集尿液标本,并处死大鼠,留取肾组织标本。检测24 h尿蛋白排泄量、血生化指标,行肾组织光镜和电镜观察肾小球病变和足突超微结果。采用定量学方法测定足突宽度。免疫组化观察足细胞裂孔膜分子nephrin表达和分布变化。结果人参皂苷Rg1低剂量组和高剂量组均能改善多柔比星肾病大鼠的肾病综合征状况。同时,人参皂苷Rg1低剂量组和高剂量组能明显改善足突融合,增加足细胞裂孔膜分子nephrin表达(P<0.05)。人参皂苷Rg1高剂量组在血生化、肾脏病理和足细胞nephrin的表达上比人参皂苷Rg1低剂量组的改善更加明显(P<0.05)。结论人参皂苷Rg1对多柔比星肾病模型有很好的保护作用,而且人参皂苷Rg1高剂量组比低剂量组治疗作用更明显。 Objective Podocyte injury is believed to be a major contributor to proteinuria, and therefore how to repair damaged podocytes has become a focus of research in recent years. The aim of this study was to investigate the therapeutic effects of ginsenoside Rg1 on adriamycin (ADR)-induced nephrotic syndrome in rats and its protection against on podocyte injuries. Methods Thirty-two SD rats were divided randomly into a blank control, an ADR nephrosis model, a low-dose ginsenoside Rg1 and a high-dose ginsenoside Rg1 group. The model of ADR-induced nephrosis was established by single intravenous injection of ADR. Urine samples were collected and renal tissues were processed at 7, 14 and 28 days. The 24 h urinary protein excretion arid blood biochemistry parameters were measured by routine methods. The glomerular morphology and podoeyte ultrastrueture were observed by light microscopy and transmission electron microscopy, respectively. The foot process width was determined by quantitative method, and the changes in the nephrin expression and distribution observed by immunohistochemlstry. Results Both low- and high-dose ginsenoside Rg1 significantly improved the ADR-induced nephritic syndrome of the rats, and remarkably reduced the degree and area of podocyte foot process effacement.It also markedly increased the expression and distribution of nephrin, more significantly in the high-dose than in the low-dose group. Conclusion Ginsenoside Rg1 could protect the kidney against ADR- induced injury, more significantly at a high dose than at a low dose.
出处 《医学研究生学报》 CAS 北大核心 2012年第6期591-596,共6页 Journal of Medical Postgraduates
关键词 人参皂苷RG1 多柔比星肾病 足细胞 NEPHRIN Ginsenoside Rg1 Adriamycin-induced nephrotic syndrome Podocyte nephrin
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  • 1Cook HT. Focal segmental glomerulosclerosis in IgA nephropathy: a result of primary podocyte injury [ J ]. Kidney International, 2011,79(6) : 581-583.
  • 2Dai CS, Saleem MA, Holzman LB, et al. Hepatocyte growth fac- tor signaling ameliorates podocyte injury and proteinuria [ J ]. Kidney International, 2010, 77( 11 ): 962-973.
  • 3汤天凤,洪亦眉,陈朝红,张明超,黎磊石,刘志红.雷公藤甲素干预白细胞介素13诱导足细胞损伤的作用研究[J].医学研究生学报,2010,23(11):1140-1144. 被引量:8
  • 4Nakhoul F, Ramadan R, Khankin E, et al. Glomerular abun- dance of nephrin and podocin in experimental nephrotie syn- drome: different effects of antiproteinuric therapies [ J ]. AM J Physiol Renal Physiol, 2005, 289(4) :F880-F890.
  • 5Gundersen H J, Seefeldt T, Osterby R. Glomerular epithelial foot processes in normal man and rats. Distribution of true width and its intra- and inter- individual variation [ J ]. Cell Tissue Res, 1980, 205(1) : 147-155.
  • 6杨念生,武庆庆,姜宗培,张锐,王芳,罗明乾,关伟明,余学清,叶任高.维甲酸抑制大鼠单侧输尿管梗阻模型肾间质纤维化[J].中华肾脏病杂志,2004,20(3):194-198. 被引量:19
  • 7Fogo AB. Mechanisms of progression of chronic kidney disease [ J ]. Pediatr Nephrol, 2007, 22 ( 12 ) :2011-2022.
  • 8Xie XS, Liu HC, Wang FP, et al. Ginsenoside Rgl Modulation on Thrombospondin-1 and Vascular Endothelial Growth Factor Expression in Early Renal Fibrogenesis in Unilateral Obstruction [J]. Phytotherapy Res, 2010, 24(11) :1581-1587.
  • 9谢席胜,刘衡川,左川,邓尧,樊均明.人参皂甙Rg1对单侧输尿管梗阻后大鼠肾间质纤维化的作用研究[J].四川大学学报(医学版),2008,39(2):218-222. 被引量:11
  • 10Xie XS, Yang M, Liu HC, et al. Ginsenoside Rgl, a major ac- tive component isolated from Panax notoginseng, restrains tubular epithelial to myofibroblast transition in vitro[J]. J Ethnopharma- col ,2009,122 ( 1 ) :35-41.

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