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安体舒通对自发性高血压大鼠肾小球纤维化的影响
引用本文:许明,杨汉东,李东峰,闵新文,陈欣.安体舒通对自发性高血压大鼠肾小球纤维化的影响[J].中国医师杂志,2010,12(3):329-332.
作者姓名:许明  杨汉东  李东峰  闵新文  陈欣
作者单位:1. 信阳市中心医院重症医学科,河南省信阳,464000
2. 郧阳医学院附属东风医院心内科
摘    要:目的观察安体舒通对自发性高血压大鼠(SHR)肾小球纤维化的影响及可能机制。方法16只14周龄雄性SHR随机等分为安体舒通组和对照组,分别以安体舒通30mg/(kg·d)及等量生理盐水灌胃12周,8只同龄雄性SD大鼠作为正常对照组,免疫组化和RT-PCR检测结缔组织生长因子(CTGF)、转化生长因子β1(TGF—β1)的表达;MASSON染色分析测量胶原容积分数(CVF);碱水解法测定羟脯氨酸(Hypro)含量。结果SHR对照组CVF(7.78±0.28)%]、Hypro(491±35.0)μg/g],CTGF(14.87±0.73)、TGF—β1(18.31±0.86)表达明显高于正常对照组分别为(4.36±0.41)%,(321±53.8)μg/g,8.40±0.67,12.04±0.71,P〈0.01];相对于SHR对照组,安体舒通组则显著降低分别为(6.35±1.12)%,(429±53.7)μg/g,13.02±0.92,16.37±1.24,P〈0.05]。结论安体舒通能明显改善SHR肾小球纤维化,其作用可能是通过阻断盐皮质激素受体和抑制CT—GF及TGF-β1的表达而实现的。

关 键 词:螺内酯/药理学  高血压/并发症  肾疾病/并发症/药物疗法  纤维化/药物疗法

Effect of spironolactone on glomerulus fibrosis of spontaneously hypertensive rats
XU Ming,YANG Han-dong,LI Dong-feng,MIN Xin-wen,CHEN Xin.Effect of spironolactone on glomerulus fibrosis of spontaneously hypertensive rats[J].Journal of Chinese Physician,2010,12(3):329-332.
Authors:XU Ming  YANG Han-dong  LI Dong-feng  MIN Xin-wen  CHEN Xin
Institution:. ( Department of Critical Medicine, Xinyang Central Hospital, Xinyang 464000, China)
Abstract:Objective To observe the effect of spironolactone on glomerulus fibrosis of spontane-ously hypertensive rats.Methods 16 fourteen-week-old male SHRs were equivalently random assigned to dium chloride for 12 weeks by gavage.8 same age male SD rats were selected as control group.CTGF and TGF-β1 were determined by immunohistochemistry and RT-PCR.CVF was measured by MASSON staining.The concentration of Hypro was detected by alkaline hydrolysis method.Results The CVF(7.78±0.28)%],Hypro(491±35.0)μg/g],and the expression of TGF-β1(18.31±0.86),CTGF(14.87±0.73)in SHR group were significantly higher than those in SD group(4.36±0.41)%,(321±53.8)μg/g,8.40±0.67,12.04±0.71,P<0.01].Compared with the SHR group,these indices in spironolactone treatment group decreased obviously(6.35±1.12)%,(429±53.7)μg/g,13.02±0.92,16.37±1.24,P<0.05].Conclusions Spironolactone significantly improved glomerulus fdarosis of SHR by blocking mineralocorticoid receptor and suppressing the expression of CTGF and TGF-βl.
Keywords:Spironolactone/PD  Hypertension/CO  Kidney Diseases/CO/DT  Fibrosis/DT
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