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1.
Acta Pharmaceutica Sinica ; (12): 105-110, 2005.
Article Dans Anglais | WPRIM | ID: wpr-241366

Résumé

<p><b>AIM</b>To investigate the inhibitory effects and mechanism of action of isoliensinine (IL) on the proliferation of porcine coronary arterial smooth muscle cells (CASMCs) induced by phenylephrine (Phen) and its mechanisms of action.</p><p><b>METHODS</b>MTT assay, immunohistochemical method and Western blotting were adopted.</p><p><b>RESULTS</b>IL (0.03 - 3 micromol x L(-1)) could inhibit the CASMCs proliferation induced by Phen (0.1 micromol x L(-1)) in a concentration-dependent manner. IL (0.1 micromol x L(-1)) antagonized Phen-induced overexpression of PDGF-beta and bFGF from 0.545 +/- 0.026 and 0.47 +/- 0.03 to 0.458 +/- 0.019 and 0.376 +/- 0.017 (P < 0.01 , P < 0.01). IL (0.1 micromol x L(-1)) also decreased c-fos, c-myc and hsp70 overexpression induced by Phen from 0.57 +/- 0.04, 0.44 +/- 0.04 and (173 +/- 36)% to 0.46 +/- 0.05, 0.372 +/- 0.021 and (115 +/- 35)% respectively (P < 0.01, P < 0.01, P < 0.01).</p><p><b>CONCLUSION</b>IL exerted antiproliferative effect on CASMCs induced by phenylephrine, and its mechanisms were related to decrease the overexpression of growth factors (PDGF-beta, bFGF), protooncogene (c-fos, c-myc) and hsp70.</p>


Sujets)
Animaux , Prolifération cellulaire , Cellules cultivées , Vaisseaux coronaires , Biologie cellulaire , Relation dose-effet des médicaments , Facteur de croissance fibroblastique de type 2 , Métabolisme , Protéines du choc thermique HSP70 , Métabolisme , Isoquinoléines , Pharmacologie , Muscles lisses vasculaires , Biologie cellulaire , Nelumbo , Chimie , Phényléphrine , Plantes médicinales , Chimie , Protéines proto-oncogènes c-fos , Métabolisme , Protéines proto-oncogènes c-myc , Métabolisme , Protéines proto-oncogènes c-sis , Métabolisme , Suidae
2.
Chinese Journal of Laboratory Medicine ; (12)2003.
Article Dans Chinois | WPRIM | ID: wpr-685498

Résumé

Objective To study the effects of russel viper venom X(RVV X)on blood coagulation protein.Methods We divide diluted protein into control and RVV-X groups,then use chromogenic substract assay to detect the activation effect of RVV-Ⅹ on coagulation factor Ⅶ,Ⅸ,Ⅹ and antithrombin,plasminogen,with or without activator.Results In RVV-Ⅹ group,the coagulation factor Ⅶ, Ⅸ and plasminogen displayed weakly enhanced chromogenesis,all P

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