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依普利酮下调 SGK-1表达抑制梗阻性肾病细胞增殖的研究

吴丽敏 陈立祥 梁丽娟 王筝 王淼 刘少伟 熊云昭 王萱 许庆友

中国药理学通报Issue(1):69-73,5.
中国药理学通报Issue(1):69-73,5.DOI:10.3969/j.issn.1001-1978.2016.01.015

依普利酮下调 SGK-1表达抑制梗阻性肾病细胞增殖的研究

Inhibitory effects of eplerenone on cell proliferation via down-regulated SGK-1 pathway in rats with unilateral ureteral obstruction

吴丽敏 1陈立祥 2梁丽娟 1王筝 1王淼 3刘少伟 1熊云昭 3王萱 1许庆友1

作者信息

  • 1. 河北医科大学研究生学院,河北 石家庄 050091
  • 2. 河北中医学院中西医结合学院内科教研室,河北省中西医结合肝肾病重点实验室,河北 石家庄 050091
  • 3. 河北中医学院中西医结合学院内科教研室,河北省中西医结合肝肾病重点实验室,河北 石家庄 050091
  • 折叠

摘要

Abstract

Aim To observe the effect of mineralocor-ticoid receptor blockade eplerenone on cell proliferation in obstructed kidney of rats. Methods Renal intersti-tial fibrotic animals were made with unilateral ureteral obstruction (UUO) and treated with eplerenone100 mg · kg - 1 · d - 1 . The kidneys were harvested on the 10th day and proliferating cell nuclear antigen ( PC-NA ), serum and glucocorticoid induced kinase-1 (SGK-1 ) and transforming growth factor-β1 ( TGF-β1 ) were detected with immunohistochemistry and Western blot. Results Renal histopathology showed large quantities extracellular matrix (ECM) accumula-tion in kidney with UUO, large numbers of inflammato-ry cells infiltrated in renal interstitium, renal tubular expansion and exfoliation of epithelial cells . The cell proliferation and ECM accumulation were inhibited in eplerenone treated rats significantly. Immunohisto-chemistry and Western blot showed that expressions of PCNA,SGK-1 and TGF-β1 were significantly up-regu-lated with UUO and down-regulated by eplerenone. Conclusion Eplerenone plays the role in inhibiting the cell proliferation and reducing ECM accumulation by down-regulating expression of SGK-1 pathway in rats with unilateral ureteral obstruction.

关键词

依普利酮/肾间质纤维化/细胞增殖/UUO/PCNA/SGK-1/TGF-β1

Key words

eplerenone/renal interstitial fibrosis/cell proliferation/UUO/PCNA/SGK-1/TGF-β1

分类

医药卫生

引用本文复制引用

吴丽敏,陈立祥,梁丽娟,王筝,王淼,刘少伟,熊云昭,王萱,许庆友..依普利酮下调 SGK-1表达抑制梗阻性肾病细胞增殖的研究[J].中国药理学通报,2016,(1):69-73,5.

基金项目

国家自然科学基金资助项目(No 81273684,81473652),河北省自然科学基金资助项目(No H2015423009) (No 81273684,81473652)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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