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Panax ginseng ameliorates airway inflammation in an ovalbumin-sensitized mouse allergic asthma model.

Authors: Kim, Dae Yong  Yang, Woong Mo 
Citation: Kim DY and Yang WM, J Ethnopharmacol. 2011 Jun 14;136(1):230-5. doi: 10.1016/j.jep.2011.04.048. Epub 2011 Apr 28.
Pubmed: (View Article at PubMed) PMID:21549818
DOI: Full-text: DOI:10.1016/j.jep.2011.04.048

ETHNOPHARMACOLOGICAL RELEVANCE: Panax ginseng (PG) is a medicinal herb that has been used to treat various immune diseases including asthma and COPD. In this study, we investigated the inhibitory mechanism of PG on asthma parameters in mice.
MATERIALS AND METHODS: BALB/c mice were sensitized with 20 µg/200 µl OVA adsorbed on 1.0mg/50 µl aluminum hydroxide gel adjuvant by i.p. injection on days 0 and 14. Mice were then challenged with 5% OVA in PBS to the nose for 30 min once a day for 3 days, from day 20 until day 22, using a nebulizer. PG (20mg/kg) or vehicle was administrated by i.p. injection once a day 10 min before every OVA challenge for 3 days. The recruitment of inflammatory cells into bronchoalveolar lavage fluid or lung tissues was measured. The expression of EMBP, Muc5ac, CD40, and CD40 ligand (CD40L) in lung tissues was investigated. In addition, the cytokines and mitogen activated protein (MAP) kinases were measured by RT-PCR and Western blot.
RESULTS AND CONCLUSIONS: PG restored the expression of EMBP, Muc5ac, CD40, and CD40L, as well as the mRNA and protein levels of interleukin (IL)-1ß, IL-4, IL-5, and tumor necrosis factor (TNF)-a. In addition, PG inhibited the numbers of goblet cells and further small G proteins and MAP kinases in bronchoalveolar lavage cells and lung tissues increased in ovalbumin-induced allergic asthma in mice. These results suggest that PG may be used as a therapeutic agent in asthma, based on reductions of various allergic responses.


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CRRD Object Information
CRRD ID: 7364729
Created: 2013-09-25
Species: All species
Last Modified: 2013-09-25
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.