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1.
Journal of Chinese Physician ; (12): 145-148, 2010.
Article in Chinese | WPRIM | ID: wpr-390430

ABSTRACT

Objective To investigate the expression of p21 and p53 in renal interstitial fibrosis rats and the effect of enalapril on it. Methods Sprague-Dawley rats were randomly divided into 3 groups, shame operation rats group, unilateral urethral obstruction and enalapril treatment group. Histological chan-ges were observed by Masson stain. The expression of p21 mRNA and p53 mRNA was detected by RT-PCR. Results With degree of interstitial fibrosis aggravating, the expression of p21 and p53 increasing,p21 and p53 expression of UUO rats at every time point were positive correlative. Enalapril can inhibit the expression of p21 and p53. Concinsion p21 and p53 expression increased in UUO rats renal cortex and enalapril can significantly inhibit its expression, p21 may participate in the pathogenesis of renal tubule-in-terstitial fibrosis through p53 pathway.

2.
Journal of Central South University(Medical Sciences) ; (12): 663-670, 2006.
Article in Chinese | WPRIM | ID: wpr-813625

ABSTRACT

OBJECTIVE@#To investigate the expression of P21 in renal interstitial fibrosis rats and the effect of enalapril on it.@*METHODS@#Sprague Dawley rats were randomly divided into 3 groups: a sham operation group,a unilateral urethral obstruction group, and an enalapril treatment group. The expression of P21 in renal tubular epithelial cells on the process was detected by immunohistochemistry at different time spots (7, 14, 21 d after UUO, sham-surgery or enalapril treatment). The expression of p21 mRNA was detected by reverse transcription-polymerase chain reaction (RT-PCR).@*RESULTS@#Seven days after the surgery, significant differences were found in P21 expression between UUO and SOR renal tubular cells. With degree of interstitial fibrosis aggravating, P21 expression increased. Enalapril can inhibit its expression.@*CONCLUSION@#In the kidney of UUO rats, P21 expression increased and enalapril possessed significant inhibitory effects on the procedure. P21 may participate in the pathogenesis of renal tubule-interstitial fibrosis.


Subject(s)
Animals , Male , Rats , Angiotensin-Converting Enzyme Inhibitors , Pharmacology , Therapeutic Uses , Enalapril , Pharmacology , Therapeutic Uses , Kidney Tubules , Metabolism , Nephrosclerosis , Drug Therapy , Metabolism , Proto-Oncogene Proteins p21(ras) , Genetics , RNA, Messenger , Genetics , Random Allocation , Rats, Sprague-Dawley , Ureteral Obstruction
3.
Journal of Central South University(Medical Sciences) ; (12): 671-675, 2006.
Article in Chinese | WPRIM | ID: wpr-813623

ABSTRACT

OBJECTIVE@#To explore the effect of p27 in the renal tubule on the process of renal interstitial fibrosis caused by unilateral ureteral obstruction (UUO) in rats, and to examine the expression changes of p27 after enalapril intervention and to interpret the anti-fibrotic mechanism.@*METHODS@#Ninety rats were randomly divided into the sham-operated group (SOR), UUO group,and UUO+enalapril treatment group [enalapril: 10 mg/(kg.d)]. The rats of each group were respectively sacrificed on 7, 14, 21 days post-operatively. The renal pathological changes were dynamically observed by HE. The expression and dynamic changes of p27 were detected by immunohistochemistry. The level of p27 mRNA were detected by RT-PCR.@*RESULTS@#The expression of p27 in renal tubular epithelial cells and p27 mRNA were strongly positive in the SOR group. With degree of interstitial fibrosis aggravating, the expression of p27 mRNA was gradually reducing. Enalapril could improve the expression of p27 on the 14th and 21st days after the UUO.@*CONCLUSION@#(1) This study supports a causative role of p27 in the formation of fibrosis of renal mesenchyme in rats with UUO. (2) The anti-fibrotic mechanism of enalapril is partly the improvement of p27 expression.


Subject(s)
Animals , Female , Rats , Angiotensin-Converting Enzyme Inhibitors , Pharmacology , Therapeutic Uses , Cyclin-Dependent Kinase Inhibitor p27 , Genetics , Enalapril , Pharmacology , Therapeutic Uses , Kidney Tubules , Metabolism , Nephrosclerosis , Drug Therapy , Metabolism , RNA, Messenger , Genetics , Random Allocation , Rats, Sprague-Dawley , Ureteral Obstruction
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