Suppressive effect of Petasites japonicus extract on ovalbumin-induced airway inflammation in an asthmatic mouse model

Petasites japonicus extract has inhibitory properties on asthma and may be used as a potent therapeutic agent for allergic lung inflammation. Asthma is a disease marked by airway inflammation. Petasites japonicus (Pj) is known as an herb for treating asthma, oxidant stress and gastric ulcer in tradi...

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Veröffentlicht in:Journal of ethnopharmacology 2011-01, Vol.133 (2), p.551-557
Hauptverfasser: Lee, Ji-Sook, Yang, Eun Ju, Yun, Chi-Young, Kim, Dong-Hee, Kim, In Sik
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Yang, Eun Ju
Yun, Chi-Young
Kim, Dong-Hee
Kim, In Sik
description Petasites japonicus extract has inhibitory properties on asthma and may be used as a potent therapeutic agent for allergic lung inflammation. Asthma is a disease marked by airway inflammation. Petasites japonicus (Pj) is known as an herb for treating asthma, oxidant stress and gastric ulcer in traditional Oriental medicine. In this study, the inhibitory effects of Pj extract on asthmatic responses were examined both in vitro and in vivo. The Pj extract was acquired from whole plants of Petasites japonicus using 80% ethanol. Cytotoxicity of the Pj extract on Jurkat cells and THP-1 cells was determined using MTT assay. ELISA was performed to determine the expression levels of cytokines, chemokines, and IgE. BALB/c mice were used for an OVA-induced asthmatic mouse model. Reactive oxygen species (ROS) production was stained with 2′,7′-dichlorofluorescein diacetate and measured by fluorescence-activated cell sorting analysis. The effects of the Pj extract on leukocyte infiltration and mucus production were determined using periodic acid-Schiff staining as well as hematoxylin and eosin staining. The Pj extract inhibits the increased release of interleukin (IL)-2, IL-4, IL-5, IL-13, and TNF-α due to house dust mite in Jurkat cells and blocks IL-6 expression in THP-1 cells without cytotoxicity. In the asthmatic mouse model, the Pj extract inhibits eosinophil infiltration, mucus hypersecretion, and IL-5 level in bronchoalveolar lavage (BAL) fluid, and it has a scavenging effect on ROS production of cells in BAL fluid. The Pj extract has suppressive properties for the pathogenesis of airway inflammation and may be used as a potent agent for the treatment of asthma.
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Asthma is a disease marked by airway inflammation. Petasites japonicus (Pj) is known as an herb for treating asthma, oxidant stress and gastric ulcer in traditional Oriental medicine. In this study, the inhibitory effects of Pj extract on asthmatic responses were examined both in vitro and in vivo. The Pj extract was acquired from whole plants of Petasites japonicus using 80% ethanol. Cytotoxicity of the Pj extract on Jurkat cells and THP-1 cells was determined using MTT assay. ELISA was performed to determine the expression levels of cytokines, chemokines, and IgE. BALB/c mice were used for an OVA-induced asthmatic mouse model. Reactive oxygen species (ROS) production was stained with 2′,7′-dichlorofluorescein diacetate and measured by fluorescence-activated cell sorting analysis. The effects of the Pj extract on leukocyte infiltration and mucus production were determined using periodic acid-Schiff staining as well as hematoxylin and eosin staining. The Pj extract inhibits the increased release of interleukin (IL)-2, IL-4, IL-5, IL-13, and TNF-α due to house dust mite in Jurkat cells and blocks IL-6 expression in THP-1 cells without cytotoxicity. In the asthmatic mouse model, the Pj extract inhibits eosinophil infiltration, mucus hypersecretion, and IL-5 level in bronchoalveolar lavage (BAL) fluid, and it has a scavenging effect on ROS production of cells in BAL fluid. 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Asthma is a disease marked by airway inflammation. Petasites japonicus (Pj) is known as an herb for treating asthma, oxidant stress and gastric ulcer in traditional Oriental medicine. In this study, the inhibitory effects of Pj extract on asthmatic responses were examined both in vitro and in vivo. The Pj extract was acquired from whole plants of Petasites japonicus using 80% ethanol. Cytotoxicity of the Pj extract on Jurkat cells and THP-1 cells was determined using MTT assay. ELISA was performed to determine the expression levels of cytokines, chemokines, and IgE. BALB/c mice were used for an OVA-induced asthmatic mouse model. Reactive oxygen species (ROS) production was stained with 2′,7′-dichlorofluorescein diacetate and measured by fluorescence-activated cell sorting analysis. The effects of the Pj extract on leukocyte infiltration and mucus production were determined using periodic acid-Schiff staining as well as hematoxylin and eosin staining. The Pj extract inhibits the increased release of interleukin (IL)-2, IL-4, IL-5, IL-13, and TNF-α due to house dust mite in Jurkat cells and blocks IL-6 expression in THP-1 cells without cytotoxicity. In the asthmatic mouse model, the Pj extract inhibits eosinophil infiltration, mucus hypersecretion, and IL-5 level in bronchoalveolar lavage (BAL) fluid, and it has a scavenging effect on ROS production of cells in BAL fluid. 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Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>Phytotherapy</subject><subject>plant extracts</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - toxicity</subject><subject>protective effect</subject><subject>reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>respiratory system</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtv1DAQgC0EotvCD-ACviBO2Y4fjR1xQhUUpEqtVHq2vPYYHOWFnSz039dhF7ghWbZm_M149JmQVwy2DFh93m5bnLYcfsdbEPoJ2TCteKUulHhKNiCUrrSS7ISc5twCgGISnpMTzoA3SsGG7O-WaUqYc9wjxRDQzXQM9BZnm-OMmbZ2Gofolkzx15zsej3QcW-73dLHoYqDXxx6amP6aR9oHEJn-97OsVBxoLasPH9fE47245Kx7B67F-RZsF3Gl8fzjNx_-vj18nN1fXP15fLDdeWk4nOlamA7VI1vLoT3VnoukfPGgVdopRRMM8U01lw3jmNgqAFE7QGD9igUF2fk3aHvlMYfC-bZ9DE77Do7YJnGaCkkE0rUhWQH0qUx54TBTCn2Nj0YBma1bVpTbJvV9poqtkvN62P3Zdej_1vxR28B3h4Bm53tQrKDi_kfV3pozWXh3hy4YEdjv6XC3N-VlwSwhmsBK_H-QGCxtY-YTHYRh6I-pvJnxo_xP4M-Akyjp70</recordid><startdate>20110127</startdate><enddate>20110127</enddate><creator>Lee, Ji-Sook</creator><creator>Yang, Eun Ju</creator><creator>Yun, Chi-Young</creator><creator>Kim, Dong-Hee</creator><creator>Kim, In Sik</creator><general>Elsevier Ireland Ltd</general><general>Amsterdam; New York: Elsevier</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20110127</creationdate><title>Suppressive effect of Petasites japonicus extract on ovalbumin-induced airway inflammation in an asthmatic mouse model</title><author>Lee, Ji-Sook ; Yang, Eun Ju ; Yun, Chi-Young ; Kim, Dong-Hee ; Kim, In Sik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c472t-7601be79d953dda4d24e229c0d7ea443181718e6289c2ef1e80036d0ef8de3723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Airway inflammation</topic><topic>animal models</topic><topic>Animals</topic><topic>Anti-Asthmatic Agents - isolation &amp; purification</topic><topic>Anti-Asthmatic Agents - pharmacology</topic><topic>Anti-Asthmatic Agents - toxicity</topic><topic>anti-inflammatory activity</topic><topic>Anti-inflammatory effect</topic><topic>antioxidant activity</topic><topic>asthma</topic><topic>Asthma - drug therapy</topic><topic>Asthma - etiology</topic><topic>Asthma - pathology</topic><topic>Asthma - physiopathology</topic><topic>Biological and medical sciences</topic><topic>bronchoalveolar lavage fluid</topic><topic>Cell Line</topic><topic>chemokines</topic><topic>cytokines</topic><topic>Cytokines - metabolism</topic><topic>cytotoxicity</topic><topic>Disease Models, Animal</topic><topic>Eosinophils</topic><topic>Ethnopharmacology</topic><topic>Female</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>immunoglobulin E</topic><topic>Immunoglobulin E - blood</topic><topic>inflammation</topic><topic>interleukin-5</topic><topic>Jurkat Cells</topic><topic>leukocytes</topic><topic>Lung - drug effects</topic><topic>Lung - pathology</topic><topic>Medical sciences</topic><topic>medicinal plants</topic><topic>Medicine, Korean Traditional</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>mucus</topic><topic>mucus hypersecretion</topic><topic>Ovalbumin - immunology</topic><topic>pathogenesis</topic><topic>Petasites - chemistry</topic><topic>Petasites japonicus</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. 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Asthma is a disease marked by airway inflammation. Petasites japonicus (Pj) is known as an herb for treating asthma, oxidant stress and gastric ulcer in traditional Oriental medicine. In this study, the inhibitory effects of Pj extract on asthmatic responses were examined both in vitro and in vivo. The Pj extract was acquired from whole plants of Petasites japonicus using 80% ethanol. Cytotoxicity of the Pj extract on Jurkat cells and THP-1 cells was determined using MTT assay. ELISA was performed to determine the expression levels of cytokines, chemokines, and IgE. BALB/c mice were used for an OVA-induced asthmatic mouse model. Reactive oxygen species (ROS) production was stained with 2′,7′-dichlorofluorescein diacetate and measured by fluorescence-activated cell sorting analysis. The effects of the Pj extract on leukocyte infiltration and mucus production were determined using periodic acid-Schiff staining as well as hematoxylin and eosin staining. The Pj extract inhibits the increased release of interleukin (IL)-2, IL-4, IL-5, IL-13, and TNF-α due to house dust mite in Jurkat cells and blocks IL-6 expression in THP-1 cells without cytotoxicity. In the asthmatic mouse model, the Pj extract inhibits eosinophil infiltration, mucus hypersecretion, and IL-5 level in bronchoalveolar lavage (BAL) fluid, and it has a scavenging effect on ROS production of cells in BAL fluid. The Pj extract has suppressive properties for the pathogenesis of airway inflammation and may be used as a potent agent for the treatment of asthma.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>21029770</pmid><doi>10.1016/j.jep.2010.10.038</doi><tpages>7</tpages></addata></record>
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subjects Airway inflammation
animal models
Animals
Anti-Asthmatic Agents - isolation & purification
Anti-Asthmatic Agents - pharmacology
Anti-Asthmatic Agents - toxicity
anti-inflammatory activity
Anti-inflammatory effect
antioxidant activity
asthma
Asthma - drug therapy
Asthma - etiology
Asthma - pathology
Asthma - physiopathology
Biological and medical sciences
bronchoalveolar lavage fluid
Cell Line
chemokines
cytokines
Cytokines - metabolism
cytotoxicity
Disease Models, Animal
Eosinophils
Ethnopharmacology
Female
General pharmacology
Humans
immunoglobulin E
Immunoglobulin E - blood
inflammation
interleukin-5
Jurkat Cells
leukocytes
Lung - drug effects
Lung - pathology
Medical sciences
medicinal plants
Medicine, Korean Traditional
Mice
Mice, Inbred BALB C
mucus
mucus hypersecretion
Ovalbumin - immunology
pathogenesis
Petasites - chemistry
Petasites japonicus
Pharmacognosy. Homeopathy. Health food
Pharmacology. Drug treatments
Phytotherapy
plant extracts
Plant Extracts - pharmacology
Plant Extracts - toxicity
protective effect
reactive oxygen species
Reactive Oxygen Species - metabolism
respiratory system
title Suppressive effect of Petasites japonicus extract on ovalbumin-induced airway inflammation in an asthmatic mouse model
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