Abstract
27 individual ginsenosides and aglycones, together with five extracts from ginseng
roots, ginseng leaves, American ginseng roots, American ginseng leaves and non-saponin
fraction from roots of Panax ginseng , were tested for their effects on protein tyrosine kinase (PTK) activation induced
by an in vitro hypoxia/reoxygenation (H/R) model in cultured human umbilical vein endothelial cells
(HUVEC). The results indicated that ginsenoside-Rb1 (3 ), -Rd (7 ), -Ra1 (1 ) and -Ro (27 ) showed significant inhibitory effects on PTK activation induced by H/R. Dose-response
experiments revealed that ginsenoside-Rb1 was the most active compound and it completely blocked PTK activation at a wide range
of concentrations. Most protopanaxadiol-type ginsenosides and some protopanaxatriol-type
saponins also showed significant effects on PTK activation. However, the crude extracts
did not protect against H/R-induced PTK activation.
Key words
Panax ginseng
- C. A. Meyer - Araliaceae - ginsenosides - hypoxia/reoxygenation - protein tyrosine
kinase - tyrosine phosphorylated proteins
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Dr. De-Qiang Dou
Department of Natural Products Chemistry
Shenyang Pharmaceutical University
103 Wenhua Road
Shenyang 110015
P. R. China
eMail: doudeqiang@yahoo.com
Fax: 86-24-83890024