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J Ethnopharmacol ; 137(3): 1542-6, 2011 Oct 11.
Article in English | MEDLINE | ID: mdl-21872652

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Panax ginseng is a precious traditional Chinese herbal medicine which has been utilized as herbal tonic for improving immunity. The active component, ginsenosides have been shown to possess various pharmacological functions including immunomodulation and cardiovascular protection. AIM OF THE STUDY: To investigate the immunomodulatory effect and anti-apoptotic effect of ginsenosides on avian influenza-infected human endothelial cells, and to present evidence for the cardiovascular protection by ginseng during influenza infection. MATERIALS AND METHODS: Human umbilical vein endothelial cells (HUVECs) were infected with avian influenza H9N2/G1 to induce IP-10 production and cell death, cells were then incubated with ginsenosides PPT and Re. The level of IP-10 and microRNA was determined by ELISA and real-time PCR respectively. Cell death was determined by MTT, TUNEL and flow cytometry. RESULTS: Ginsenoside metabolite protopanaxatriol showed significant suppression effect on IP-10 production upon H9N2/G1 infection through up-regulation of miR-15b expression. In addition, ginsenoside-induced cytoprotection was reflected in the increase of cell viability. Data from flow cytometry analysis and TUNEL assay also showed that ginsenoside Re could protect ECs from H9N2/G1-induced apoptosis and DNA damage. CONCLUSIONS: This report further supports the traditional belief for immunomodulatory effects of ginseng, also demonstrated the partial protective mechanism of ginsenosides on avian influenza infection and its related endothelial dysfunction.


Subject(s)
Apoptosis/drug effects , Chemokine CXCL10/metabolism , Ginsenosides/pharmacology , Human Umbilical Vein Endothelial Cells/drug effects , Immunologic Factors/pharmacology , Inflammation Mediators/metabolism , Influenza A Virus, H9N2 Subtype/pathogenicity , Sapogenins/pharmacology , Cell Survival/drug effects , Cells, Cultured , Cytoprotection , Enzyme-Linked Immunosorbent Assay , Flow Cytometry , Human Umbilical Vein Endothelial Cells/immunology , Human Umbilical Vein Endothelial Cells/pathology , Human Umbilical Vein Endothelial Cells/virology , Humans , In Situ Nick-End Labeling , MicroRNAs/metabolism , Real-Time Polymerase Chain Reaction , Transfection
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