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氟伐他汀对5/6肾切除大鼠肾脏的保护作用 被引量:2

Renoprotective Effect of Fluvastatin on 5/6 Nephrectomized Rats
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摘要 目的 :探讨羟甲基戊二酰辅酶 A( HMG- Co A)还原酶抑制剂氟伐他汀 ( fluvastatin)对 5 /6肾切除大鼠肾脏的保护作用。方法 :将 5 /6肾切除大鼠 2 4只随机均分为 5 /6肾切除组 ,模型组 ( n=1 2 )和氟伐他汀治疗的 5 /6肾切除组 ,治疗组 ( n=1 2 ) ,另设假手术组作为对照组 ( n=6)。处理 1 3周后检测尿蛋白排泄率、血清尿素氮、肌酐、总胆固醇和甘油三酯含量 ,光镜和电镜检查肾形态改变并计算肾小球硬化指数。结果 :氟伐他汀治疗组大鼠尿蛋白排泄率、血清尿素氮和肌酐水平较模型组明显降低 ,肾脏病变和肾小球硬化程度明显减轻。结论 :氟伐他汀对 5 Objective: To investigate the renoprotective effect of fluvastatin, a 3 hydroxy 3 methylglutaryl coenzyme A reductase inhibitor (HCRI), on 5/6 nephrectomized rats. Methods: Twenty four 5/6 nephrectomized (NX) rats were randomly divided into 5/6 NX rats (model group, n =12) and fluvastatin treated 5/6 NX rats (treatment group, n =12), and sham operated rats served as control (sham operation group, n =6). After fluvastatin was orally administered(7 mg·kg -1 ·d -1 ) for 13 weeks, urinary protein excretion, BUN, serum creatinine, total cholesterol(TC), and triglyceride(TG) contents were determined. The renal pathological lesion and glomerular sclerosis index (GSI) were studied. Results:The urinary protein excretion, BUN, and serum creatinine levels in treatment group were significantly lower than those in model group. Fluvastatin markedly ameliorated the renal pathological lesion and glomerular sclerosis. Conclusion: Fluvastatin shows a renoprotective effect on 5/6 nephrectomized rats.
出处 《吉林大学学报(医学版)》 CAS CSCD 北大核心 2003年第6期729-732,共4页 Journal of Jilin University:Medicine Edition
基金 国家自然科学基金资助课题 (39870 31 2
关键词 羟甲基戊二酰基COA还原酶抑制剂 氟伐他汀 肾小球硬化症 局灶性 肾功能衰竭 肾脏保护 Hydroxymethylglutaryl CoA reductase inhibitors Fluvastatin Glomerulosclerosis, focal Kidney failure, chronic
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  • 1[1]Oda H, Keane WF. Recent advances in statins and the kidney [J]. Kidney Int,1999,56(Suppl 71):S2-S5.
  • 2[2]Raij L, Azar S, Keane W. Mesangial immune injury, hypertension and progressive glomerular damage in Dahl rats [J]. Kidney Int, 1984,26:137-143.
  • 3[3]Fogo AB. Mesangial matrix modulation and glomerulosclerosis[J]. Exp Nephrol, 1999,7:147-159.
  • 4[4]Nogaki F,Muso E,Yashiro M,et al. Direct inhibitory effects of simvastatin on matrix accumulation in cultured murine mesangial cells [J]. Kidney Int, 1999, 56(Suppl 71):S198-S201.
  • 5[5]Kim SI, Han DC, Lee HB. Lovastatin inhibits transforming growth factor-β1 expression in diabetic rat glomeruli and cultured mesangial cells [J]. J Am Soc Nephrol, 2000,11:80-87.
  • 6[6]Bruijn JA, Roos A, de Geus B, et al. Transforming growth factor-β and the glomerular extracellular matrix in renal pathology [J]. J Lab Clin Med, 1994, 123:34-47.
  • 7[7]Eng E, Floege J, Young BA, et al. Does extracellular matrix expansion in glomerular disease require mesangial cell proliferation? [J] Kidney Int, 1994,45(Suppl 1):S45-S47.

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  • 2袁勤生 王志友 等.邻苯三酚自氧化法测定超氧化物歧化酶的活性[J].医药工业,1983,1:16-19.
  • 3Brown MS, Goldstein JL. Lipoprotein metabolism in the macrophage implications for cholesterol depositron in atherosclerosis [J]. Annu Rever Biochem, 1983, 52: 223-261.
  • 4Xiong Z, Ruan-Varghese Z, Powis SH, et al. Human mesangial cells express inducible macrophage scavwnger receptor [J]. Kidney Int, 1999, 56: 440-451.
  • 5Kasike BL, O' Donnell MP, Lee H, et al. Impact of dietary fatty acid supplementation on renal injure in obese Zucker rats.Kidney Int, 1991, 39: 1125-1134.
  • 6Martin - Mateo MC, Canto - Jafiez E, Barrero - Martinez MJ.Oxidative stress and enzyme activity in ambulatory renal patient undergoing continuous peritoneal dialysis [J]. Renal Failure 1998,20: 117.
  • 7Roob JM, Rabold T, Hayn M, et al. Exvivo low- density lipoprotein oxidizabiliby and in vivo Lipid peroxidation in patients on CAPD [J]. Kidney Int 2001, 78. s128.
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