期刊论文详细信息
International Journal of Molecular Sciences
Inhibition of Extracellular Signal-Regulated Kinases Ameliorates Hypertension-Induced Renal Vascular Remodeling in Rat Models
Li Jing1  Jianzhong Zhang1  Jinping Sun1  Fengying Guo1  Xin An2  Kan Yang3 
[1] Department of Pathology, Basic Medical College, Ningxia Medical University, Yinchuan 750004, Ningxia, China; E-Mails:;Department of Pathology, First Hospital of Handan, Handan 056002, Hebei, China; E-Mail:;Department of Ophthalmology, Lanzhou First People’s Hospital, Lanzhou 730000, Gansu, China; E-Mail:
关键词: artery;    extracellular signal-regulated kinase;    hypertension;    kidney SHR;    vascular remodeling;   
DOI  :  10.3390/ijms12128333
来源: mdpi
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【 摘 要 】

The aim of this study is to investigate the effect of the extracellular signal-regulated kinases 1/2 (ERK1/2) inhibitor, PD98059, on high blood pressure and related vascular changes. Blood pressure was recorded, thicknesses of renal small artery walls were measured and ERK1/2 immunoreactivity and erk2 mRNA in renal vascular smooth muscle cells (VSMCs) and endothelial cells were detected by immunohistochemistry and in situ hybridization in normotensive wistar kyoto (WKY) rats, spontaneously hypertensive rats (SHR) and PD98059-treated SHR. Compared with normo-tensive WKY rats, SHR developed hypertension at 8 weeks of age, thickened renal small artery wall and asymmetric arrangement of VSMCs at 16 and 24 weeks of age. Phospho-ERK1/2 immunoreactivity and erk2 mRNA expression levels were increased in VSMCs and endothelial cells of the renal small arteries in the SHR. Treating SHR with PD98059 reduced the spontaneous hypertension-induced vascular wall thickening. This effect was associated with suppressions of erk2 mRNA expression and ERK1/2 phosphorylation in VSMCs and endothelial cells of the renal small arteries. It is concluded that inhibition of ERK1/2 ameliorates hypertension induced vascular remodeling in renal small arteries.

【 授权许可】

CC BY   
© 2011 by the authors; licensee MDPI, Basel, Switzerland.

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