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一氧化氮与腹膜透析腹膜血管增生的关系

Relationship of nitric oxide and angiogenesis in peritoneal dialysis
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摘要 目的探讨阿托伐他汀及螺内酯对腹膜透析时血管增生的影响及其机制。方法将40只雄性Wistar大鼠随机分成4组,每组10只。A组为对照组,每日腹腔内注入0.9%生理盐水20ml。B、C、D组于腹腔内每日注入4.25%百特透析液20ml,并于试验第7、14、21、28天分别加入乳酸盐红霉素6.25万U,同时,C组给予螺内酯100mg·kg-1·d-1灌胃,D组给予阿托伐他汀20mg·kg-1·d-1灌胃。30d后留取各组大鼠腹膜用免疫组织化学法检测腹膜血管增生情况,硝酸还原法检测腹膜透析液中一氧化氮(NO)浓度。结果与A组相比,B、C、D组腹膜血管增生显著加重,腹膜透析液NO浓度升高(P〈0.05);与B组相比,C、D组腹膜血管增生显著减轻,腹膜透析液NO浓度降低(P〈0.05)。结论阿托伐他汀及螺内酯能有效的减少腹膜血管增生,可能与下调NO表达有关。 Objective To investigate the effect of atorvastatin and spironolactone on angiogenesis and its mechanisms in peritoneal dialysis. Methods 40 male wistar rats were divided into 4 groups randomly, 10 in each group. Rats in group A were intraperitoneally infected with 0. 9% normal saline daily as control. Rats in group B,C and D were intraperitoneally injected with 4. 25% batter dialysate 20 ml daily,and infected with erythromycin lactobionate 62 500 units on the 7th, 14th, 21st and 28th days of the treatment. Additionally, rats in group C were given spironolactone 100 mg/kg daily by gastric gavage, those in group D were given atrovastatin 20 mg/kg daily by gastric gavage. Rats were sacrificed on the 30th day of the treatment. Angiogenesis expression by immunohistochemistry in peritoneal membrane were examined in these rats. Nitrate reductase assay the concentration of nitric oxide (NO) in peritoneal dialysis solution. Results Angiogenesis of peritoneal membrane was eminent in group B,C, D than in group A, so did the NO in the peritoneal fluid (P〈0. 05). Compared with group B, peritoneal angiogenesis significantly reduced, NO concentration decreased in group C and D (P〈 0. 05). Conclusion Atorvastatin and spironolactone can effectively reduce the peritoneal angiogenesis, may be associated with reduced expression of NO.
作者 张鹂 郭志勇
出处 《临床肾脏病杂志》 2010年第5期229-231,共3页 Journal Of Clinical Nephrology
关键词 腹膜透析 阿托伐他汀 螺内酯 一氧化氮 Peritoneal dialysis Atorvastatin Spironolactorne Nitric oxide
作者简介 通讯作者:郭志勇,E-mail:guozhiyong@smmu.edu.cn.
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参考文献11

  • 1张琼,张士胜,王玲.一氧化氮与血管生成的研究进展[J].国际眼科杂志,2007,7(3):788-790. 被引量:13
  • 2张鹂,李英南,吕海涛,郝丽荣.阿托伐他汀与螺内酯对腹膜纤维化的作用研究[J].中国血液净化,2009,8(8):437-440. 被引量:2
  • 3Kimura H, Esumi H. Reciprocal regulation between nitric oxide and vascular. Endothelial growth factor in angiogenesis. Acta Biochimica Polonica, 2003,50 : 49-59.
  • 4Fukumura D, Gohongi T, Kadambi A, et al. Predominant role of endothelial nitric oxide synthase invascular endotllelial growth factor-induced an giogensesis an dvascular permeability. Proc Natl Acad Sci USA,2001,98:2604-2609.
  • 5Shen BQ, Lee DY, Zioncheck TF. Vascular endothelial growth factor veins endothelial nitric-oxide synthase expression via a KDR/FIk-1 receptor an d a protein kinase C signaling pathway. J Biol Chem, 1999,274 : 33057-33063.
  • 6黄清玲,郑大利,张声,林建银.原发性肝癌中结构型一氧化氮合酶mRNA的表达及其意义[J].中华肿瘤杂志,2003,25(3):250-254. 被引量:12
  • 7Fideler LR, Bachetti T, Leiper J, et al. The ADMA/DDAH path way regulates VEGF-mediated angiogenesis. Arterioscler Thromb Vasc Biol,2009,29 : 2117-2124.
  • 8Jaumdally R.l,Goon PK, Varma C, et al. Effects of atorvastatin on circulating CD34^+/CD133^+/CD45^-progenitor cells and indices of angiogenesis (vascular endothelial growth factor and the anglo poietins 1 and 2) in atherosclerotic vascular disease and diabetes mellitus. Intern Med, 2010,267 : 385-393.
  • 9周卿,陈书艳.他汀类药物对血管新生作用及机制的研究[J].国际心血管病杂志,2006,33(1):45-48. 被引量:9
  • 10Ozbek E,Cekmen M, Ilbey YO, et al. Atorvastatin prevents gen tamicin-induced renal damage in rats through the inhibition of p38-MAPK and NF-kappaB pathways. Ren Fail, 2009, 31:382- 392.

二级参考文献67

  • 1赵士芳,刘雁鸣,平飞云,胡济安,刘建华.口腔癌中诱导型一氧化氮合酶与血管内皮生长因子表达关系的研究[J].中华口腔医学杂志,2001,36(6):64-66. 被引量:6
  • 2郑大利,黄清玲,张声,林建银.肝细胞癌中血管内皮生长因子和cNOS与血管生成及细胞增殖的关系[J].解剖学报,2005,36(1):47-51. 被引量:3
  • 3史雪辉,何守志.诱导型一氧化氮合酶在大鼠脉络膜新生血管中的表达及其与血管生成的关系[J].眼科新进展,2006,26(12):885-888. 被引量:3
  • 4Wong TY, Phillips AO, Witowski J, etal. Glucose-mediated induction of TGF-betal and MCP-1 in mesothelial cells in vitro is osmolality and polyol pathway dependent [J]. Kidney Int, 2003, 63:1404-1416.
  • 5Tang S, Leung JC, Chan LY, etal. Regulation of complement C3 and C4 synthesis in human peritoneal mesothelial cells by peritoneal dialysis fluid[J].Clin Exp Immunol, 2004, 136:85-94.
  • 6MiricG, DallemagneC, EndreZ, etal. Reversal of cardiacand renalfibrosis bypirfenidone and spironolactone in streptozotocin diabetica rats[J]. Br Jp harmacol, 2001, 133:687-694.
  • 7Kim SI, Kim HJ, Han DC, etal. Effect of Iovastatin on small 6TP binding proteinsand TGF - β1 and fibronectin expression[J]. Kidney Int, 2000,58:588-592.
  • 8Rupe rez M, Rodrigues-Df ez R, Blanco-Colio LM, et al. HMG-CoA reductase inhibitors decrease angiotensin II- induced vascular fibrosis: role of RhoA/ROCK and MAPK pathways[J].Hypertension, 2007 ,50:377-383.
  • 9[1]Kureishi Y,Luo Z,Shiojima I,et al.The HMG-CoA reductase inhibitor simvastatin activates the protein kinase Akt and promotes angiogenesis in normocholesterolemic animals[J].Nat Med,2000,6(9):1004-1010.
  • 10[2]Dimmeler S,Aicher A,Vasa M,et al.HMG-CoA reductase inhibitors (statins) increase endothelial progenitor cells via the PI 3-kinase/Akt pathway[J].J Clin Invest,2001,108(3):391-397.

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