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Journal of Central South University(Medical Sciences) ; (12): 300-307, 2009.
Article Dans Chinois | WPRIM | ID: wpr-814212

Résumé

OBJECTIVE@#To investigate the effect of cordyceps sinensis (CS) extract and losartan (Los) on the expression of Klotho (Kl), P53, P21, and apoptosis in renal tubular epithelial cell NRK-52E induced by angiotensin II (Ang II), and to elucidate its therapeutical mechanism in Ang II induced renal tubular epithelial cell apoptosis.@*METHODS@#NRK-52E cells were incubated with CS with or without Ang II for 24 hours. Experimental groups were divided according to the increasing concentrations of CS:0 (serving as controls), 5, 10, 20, 40, and 80 mg/L. The optimal concentration of CS was selected and cells were divided into 5 groups: controls, Ang II (1*10(-8) mol/L), Ang II (1*10(-8) mol/L)+CS (40 mg/L), Ang II (1*10(-8) mol/L)+Los (1*10(-5) mol/L), and Ang II (1*10(-8) mol/L)+CS (40 mg/L)+Los (1*10(-5) mol/L). After 24 hours, cell proliferation was evaluated by MTT assay. The mRNA and protein expression of Kl, P53 and P21 were measured by RT-PCR. Activity of caspase-3 was evaluated by caspase-3 activity assay Kit. Cell apoptosis was determined by Annexin V-FITC/PI double staining and flow cytometry.@*RESULTS@#Certain concentrations of CS promoted the proliferation of NRK-52E cells and increased cells proliferation inhibited by Ang II (P0.05).@*CONCLUSION@#CS can increase the expression of Kl down-regulated by Ang II, decrease P53 and P21 expression and caspase-3 activity, and reduce Ang II induced NRK-52E cell apoptosis, which may be part of its mechanism of the protective effects on hypertensive renal damage.


Sujets)
Humains , Angiotensine-II , Pharmacologie , Apoptose , Caspase-3 , Génétique , Métabolisme , Cellules cultivées , Cordyceps , Chimie , Inhibiteur p21 de kinase cycline-dépendante , Génétique , Métabolisme , Médicaments issus de plantes chinoises , Pharmacologie , Cellules épithéliales , Biologie cellulaire , Métabolisme , Glucuronidase , Génétique , Métabolisme , Tubules rénaux , Biologie cellulaire , Métabolisme , Losartan , Pharmacologie , ARN messager , Génétique , Métabolisme , Protéine p53 suppresseur de tumeur , Génétique , Métabolisme
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