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螺内酯对实验大鼠肝组织TGFβ1、PDGF-BB及α-SMA表达的影响 被引量:11

The effect of spironolactone on the expression of TGF-β_1 , PDGF-BB and α-SMA in hepatic fibrosis tissues in rats
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摘要 目的 探讨螺内酯预防肝纤维化的作用机制。方法 SD大鼠 90只 ,随机分为 3组。正常对照组 (8只 ) :正常饮食 ,皮下注射花生油 ;模型组 (42只 ) :复合因素制成肝纤维化模型 ;螺内酯预防组 (40只 ) :造模方法同模型组 ,螺内酯 10 0mg·kg- 1·d- 1灌胃。分别于第 2周、4周、6周、8周末随机处死 8只大鼠 ,取肝组织用免疫组化法检测各组肝组织内转化生长因子 β1(TGFβ1)、血小板衍生生长因子 (PDGF BB)及α 平滑肌动蛋白 (α SMA)含量。结果 螺内酯预防组TGFβ1、PDGF BB及α SMA在肝组织中的表达均较模型组明显减少 (P <0 .0 5或P <0 .0 1)。 结论 螺内酯可通过降低TGFβ1、PDGF Objective To investigate the preventive effect of spironolactone on hepatic fibrosis. Methods Ninety SD rats were randomly divided into three groups. Control group consisted of 8 rats that , fed by normal food, were injected with peanut oil subcutaneously. Model group consisted of 42 rats whose liver fibrosis was induced by compound factors. Spiro nolactone-prevention group consisted of 40 rats that were given 100 mg·kg -1 spironolactone per day, by the same methods of making models as those of the model group. At the end of weeks 2, 4, 6 and 8, 8 rats were randomly taken out of model group and spironol actone group and then were sacrificed. The expressions of TGF- β 1 , PDGF- BB and α -SMA in hepatic tissues were detected with immunohistochemical met hods. Results The expressions of TGF- β 1 , PDGF-BB a nd α -SMA in spironolactone group decreased greatly than those in model gro up ( P <0.05 or P <0.01). Conclusion Spironolactone may prevent the formation of hepa tic fibrosis by decreasing the secretion of TGF- β 1 and PDGF-BB and inhi biting the activation of hepatic stellate cell .
出处 《西安交通大学学报(医学版)》 CAS CSCD 北大核心 2004年第1期64-66,75,共4页 Journal of Xi’an Jiaotong University(Medical Sciences)
关键词 螺内酯 实验 大鼠 肝组织 TGFΒ1 PDGF-BB α-SMA 肝纤维化 转化生长因子β1 血小板衍生生长因子 Α-平滑肌动蛋白 肝星状细胞 spironolactone hepatic fibrosis transforming gro wth factor- β1 platelet-derived growth factor-BB α -smooth muscle actin hepatic stellate cell (HSC)
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  • 1吴平生 梁欣伟 戴云 等.肝脏和肺脏醛固酮合成酶基因CYP11B2mRNA的表达[J].中华医学杂志,1998,78(8):620-621.
  • 2Brilla CG, Zhou G, Weber KT. Aldosterone and collagen synthesis in cultured adult rat cardiac fibroblasts [J]. FASEB J, 1992,6(5):A1914.
  • 3Funder JW. Aldosterone, salt and cardiac fibrosis [J]. Clin Exp Hypertens, 1997,19(5-6):885-899.
  • 4Brilla CG, Weber KT. Mineralocorticoid excess, dietary sodium, and myocardial fibrosis [J]. J Lab Clin Med, 1992,120(6):893-901.
  • 5Brilla CG, Weber KT. Prevention of myocardial fibrosis in hypertension:role of fibroblast corticoid receptors and spironolactone [J]. Faseb J,1991,5(3):a1256.
  • 6Benetos A, Lacolley P, Safar ME. Prevention of aortic fibrosis by spironolactone in spontaneously hypertensive rats [J]. Arterioscler Thromb Vasc Biol, 1997,17(6):1152-1156.
  • 7MacFadyen RJ, Barr CS, Struthers AD. Aldosteroneblockade reduces vascular collagen turnover, improves heart rate variability and reduces early morning rise in heart rate in heart failure patients [J]. Cardiovasc Res, 1997,35(1):30-34.
  • 8Duval D, Funder JW. The binding of tritiated aldosterone in the rat liver cytosol [J]. Endocrinology, 1974,94(2):575.
  • 9Epstein M. Aldosterone and the hypertensive kidney: its emerging role as a mediator of progressive renal dysfunction: a paradigm shift [J]. J Hypertens, 2001,19(5):829-842.
  • 10Monder C. Heterogeneity of 11β-hydroxysteroid dehydrogenase in rat tissues [J]. J Steroid Biochem Mol Biol, 1991,40(4-6):533-536.

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