Immunomodulatory activity of red ginseng against influenza A virus infection.
Identifieur interne : 000F36 ( Main/Merge ); précédent : 000F35; suivant : 000F37Immunomodulatory activity of red ginseng against influenza A virus infection.
Auteurs : Jong Seok Lee [États-Unis] ; Hye Suk Hwang [États-Unis] ; Eun-Ju Ko [États-Unis] ; Yu-Na Lee [États-Unis] ; Young-Man Kwon [États-Unis] ; Min-Chul Kim [États-Unis] ; Sang-Moo Kang [États-Unis]Source :
- Nutrients [ 2072-6643 ] ; 2014.
Descripteurs français
- KwdFr :
- Administration par voie orale, Animaux, Antiviraux (pharmacologie), Cellules épithéliales (), Cellules épithéliales (métabolisme), Espèces réactives de l'oxygène, Extraits de plantes (pharmacologie), Femelle, Humains, Immunomodulation, Infections à Orthomyxoviridae (traitement médicamenteux), Lignée cellulaire, Liquide de lavage bronchoalvéolaire (), Modèles animaux de maladie humaine, Panax (), Pneumopathie infectieuse (traitement médicamenteux), Pneumopathie infectieuse (virologie), Poumon (), Poumon (cytologie), Souris, Souris de lignée BALB C, Stress oxydatif (), Viabilité microbienne (), Virus de la grippe A ().
- MESH :
- cytologie : Poumon.
- métabolisme : Cellules épithéliales.
- pharmacologie : Antiviraux, Extraits de plantes.
- traitement médicamenteux : Infections à Orthomyxoviridae, Pneumopathie infectieuse.
- virologie : Pneumopathie infectieuse.
- Administration par voie orale, Animaux, Cellules épithéliales, Espèces réactives de l'oxygène, Femelle, Humains, Immunomodulation, Lignée cellulaire, Liquide de lavage bronchoalvéolaire, Modèles animaux de maladie humaine, Panax, Poumon, Souris, Souris de lignée BALB C, Stress oxydatif, Viabilité microbienne, Virus de la grippe A.
English descriptors
- KwdEn :
- Administration, Oral, Animals, Antiviral Agents (pharmacology), Bronchoalveolar Lavage Fluid (chemistry), Cell Line, Disease Models, Animal, Epithelial Cells (drug effects), Epithelial Cells (metabolism), Female, Humans, Immunomodulation, Influenza A virus (drug effects), Lung (cytology), Lung (drug effects), Mice, Mice, Inbred BALB C, Microbial Viability (drug effects), Orthomyxoviridae Infections (drug therapy), Oxidative Stress (drug effects), Panax (chemistry), Plant Extracts (pharmacology), Pneumonia (drug therapy), Pneumonia (virology), Reactive Oxygen Species.
- MESH :
- chemical , pharmacology : Antiviral Agents, Plant Extracts.
- chemistry : Bronchoalveolar Lavage Fluid, Panax.
- cytology : Lung.
- drug effects : Epithelial Cells, Influenza A virus, Lung, Microbial Viability, Oxidative Stress.
- drug therapy : Orthomyxoviridae Infections, Pneumonia.
- metabolism : Epithelial Cells.
- virology : Pneumonia.
- Administration, Oral, Animals, Cell Line, Disease Models, Animal, Female, Humans, Immunomodulation, Mice, Mice, Inbred BALB C, Reactive Oxygen Species.
Abstract
Ginseng herbal medicine has been known to have beneficial effects on improving human health. We investigated whether red ginseng extract (RGE) has preventive effects on influenza A virus infection in vivo and in vitro. RGE was found to improve survival of human lung epithelial cells upon influenza virus infection. Also, RGE treatment reduced the expression of pro-inflammatory genes (IL-6, IL-8) probably in part through interference with the formation of reactive oxygen species by influenza A virus infection. Long-term oral administration of mice with RGE showed multiple immunomodulatory effects such as stimulating antiviral cytokine IFN-γ production after influenza A virus infection. In addition, RGE administration in mice inhibited the infiltration of inflammatory cells into the bronchial lumens. Therefore, RGE might have the potential beneficial effects on preventing influenza A virus infections via its multiple immunomodulatory functions.
DOI: 10.3390/nu6020517
PubMed: 24473234
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<term>Animals</term>
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<term>Bronchoalveolar Lavage Fluid (chemistry)</term>
<term>Cell Line</term>
<term>Disease Models, Animal</term>
<term>Epithelial Cells (drug effects)</term>
<term>Epithelial Cells (metabolism)</term>
<term>Female</term>
<term>Humans</term>
<term>Immunomodulation</term>
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<term>Lung (cytology)</term>
<term>Lung (drug effects)</term>
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<term>Orthomyxoviridae Infections (drug therapy)</term>
<term>Oxidative Stress (drug effects)</term>
<term>Panax (chemistry)</term>
<term>Plant Extracts (pharmacology)</term>
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<term>Pneumonia (virology)</term>
<term>Reactive Oxygen Species</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Administration par voie orale</term>
<term>Animaux</term>
<term>Antiviraux (pharmacologie)</term>
<term>Cellules épithéliales ()</term>
<term>Cellules épithéliales (métabolisme)</term>
<term>Espèces réactives de l'oxygène</term>
<term>Extraits de plantes (pharmacologie)</term>
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<term>Infections à Orthomyxoviridae (traitement médicamenteux)</term>
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<term>Liquide de lavage bronchoalvéolaire ()</term>
<term>Modèles animaux de maladie humaine</term>
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<term>Pneumopathie infectieuse (traitement médicamenteux)</term>
<term>Pneumopathie infectieuse (virologie)</term>
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<term>Poumon (cytologie)</term>
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<term>Souris de lignée BALB C</term>
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<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Epithelial Cells</term>
<term>Influenza A virus</term>
<term>Lung</term>
<term>Microbial Viability</term>
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<term>Cellules épithéliales</term>
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<term>Femelle</term>
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<term>Immunomodulation</term>
<term>Lignée cellulaire</term>
<term>Liquide de lavage bronchoalvéolaire</term>
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<front><div type="abstract" xml:lang="en">Ginseng herbal medicine has been known to have beneficial effects on improving human health. We investigated whether red ginseng extract (RGE) has preventive effects on influenza A virus infection in vivo and in vitro. RGE was found to improve survival of human lung epithelial cells upon influenza virus infection. Also, RGE treatment reduced the expression of pro-inflammatory genes (IL-6, IL-8) probably in part through interference with the formation of reactive oxygen species by influenza A virus infection. Long-term oral administration of mice with RGE showed multiple immunomodulatory effects such as stimulating antiviral cytokine IFN-γ production after influenza A virus infection. In addition, RGE administration in mice inhibited the infiltration of inflammatory cells into the bronchial lumens. Therefore, RGE might have the potential beneficial effects on preventing influenza A virus infections via its multiple immunomodulatory functions. </div>
</front>
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