Inhibitory effects of Rumex japonicus Houtt. on the development of atopic dermatitis-like skin lesions in NC/Nga mice

Summary Background  Rumex japonicus Houtt. (RJH) is one of the herbs used in Eastern countries for the treatment of atopic dermatitis (AD). It has been shown to have an antioxidative effect in human skin disease. Objectives  To examine whether RJH extract (RJH‐E) suppresses the development of AD‐lik...

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Veröffentlicht in:British journal of dermatology (1951) 2006-07, Vol.155 (1), p.33-38
Hauptverfasser: Lee, H-S., Kim, S-K., Han, J-B., Choi, H-M., Park, J-H., Kim, E-C., Choi, M-S., An, H-J., Um, J-Y., Kim, H-M., Min, B-I.
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container_end_page 38
container_issue 1
container_start_page 33
container_title British journal of dermatology (1951)
container_volume 155
creator Lee, H-S.
Kim, S-K.
Han, J-B.
Choi, H-M.
Park, J-H.
Kim, E-C.
Choi, M-S.
An, H-J.
Um, J-Y.
Kim, H-M.
Min, B-I.
description Summary Background  Rumex japonicus Houtt. (RJH) is one of the herbs used in Eastern countries for the treatment of atopic dermatitis (AD). It has been shown to have an antioxidative effect in human skin disease. Objectives  To examine whether RJH extract (RJH‐E) suppresses the development of AD‐like skin lesions in NC/Nga mice, which are induced by the repeated application of picryl chloride (PC). Methods  The efficacy of RJH‐E in NC/Nga mice was assessed by measuring symptom severity, scratching behaviour, Staphylococcus aureus numbers on an ear, and serum levels of IgE, interleukin (IL)‐4 and interferon (IFN)‐γ. Results  Oral administration of RJH‐E to NC/Nga mice treated with PC inhibited the development of AD‐like skin lesions as exemplified by a significant decrease in total skin symptom severity scores, and a decrease in hypertrophy, hyperkeratosis and infiltration of inflammatory cells in the skin. The scratching behaviour and numbers of S. aureus, which are known to be exacerbated in AD, were also significantly reduced by RJH‐E. No significant change was observed in the serum levels of IFN‐γ, whereas IgE and IL‐4 levels were significantly reduced by RJH‐E. Conclusions  These results suggest that RJH‐E inhibits the development of AD‐like skin lesions in NC/Nga mice by suppressing the T‐helper 2 cell response. Our results indicate that RJH treatment could provide an effective alternative therapy for the management of AD.
doi_str_mv 10.1111/j.1365-2133.2006.07303.x
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(RJH) is one of the herbs used in Eastern countries for the treatment of atopic dermatitis (AD). It has been shown to have an antioxidative effect in human skin disease. Objectives  To examine whether RJH extract (RJH‐E) suppresses the development of AD‐like skin lesions in NC/Nga mice, which are induced by the repeated application of picryl chloride (PC). Methods  The efficacy of RJH‐E in NC/Nga mice was assessed by measuring symptom severity, scratching behaviour, Staphylococcus aureus numbers on an ear, and serum levels of IgE, interleukin (IL)‐4 and interferon (IFN)‐γ. Results  Oral administration of RJH‐E to NC/Nga mice treated with PC inhibited the development of AD‐like skin lesions as exemplified by a significant decrease in total skin symptom severity scores, and a decrease in hypertrophy, hyperkeratosis and infiltration of inflammatory cells in the skin. The scratching behaviour and numbers of S. aureus, which are known to be exacerbated in AD, were also significantly reduced by RJH‐E. No significant change was observed in the serum levels of IFN‐γ, whereas IgE and IL‐4 levels were significantly reduced by RJH‐E. Conclusions  These results suggest that RJH‐E inhibits the development of AD‐like skin lesions in NC/Nga mice by suppressing the T‐helper 2 cell response. Our results indicate that RJH treatment could provide an effective alternative therapy for the management of AD.</description><identifier>ISSN: 0007-0963</identifier><identifier>EISSN: 1365-2133</identifier><identifier>DOI: 10.1111/j.1365-2133.2006.07303.x</identifier><identifier>PMID: 16792749</identifier><identifier>CODEN: BJDEAZ</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Allergic diseases ; Animals ; atopic dermatitis ; Biological and medical sciences ; Dermatitis, Atopic - drug therapy ; Dermatitis, Atopic - immunology ; Dermatitis, Atopic - microbiology ; Dermatology ; Female ; IgE ; Immunoglobulin E - blood ; Immunopathology ; Interferon-gamma - blood ; interferon-γ ; interleukin-4 ; Interleukin-4 - blood ; Liver Function Tests ; Medical sciences ; Mice ; Mice, Mutant Strains ; Models, Animal ; NC/Nga mice ; Phytotherapy - methods ; Picryl Chloride ; Plant Extracts - therapeutic use ; Plant Roots ; Plants, Medicinal ; Rumex ; Rumex japonicus Houtt ; Skin - drug effects ; Skin allergic diseases. Stinging insect allergies ; Staphylococcal Infections - complications ; Staphylococcal Infections - drug therapy ; Staphylococcus aureus - isolation &amp; purification ; Treatment Outcome</subject><ispartof>British journal of dermatology (1951), 2006-07, Vol.155 (1), p.33-38</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3863-d1c3de016c0de87aa61328d93d273e44be01549c401ea4295d8007c1994077de3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2133.2006.07303.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2133.2006.07303.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17848242$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16792749$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, H-S.</creatorcontrib><creatorcontrib>Kim, S-K.</creatorcontrib><creatorcontrib>Han, J-B.</creatorcontrib><creatorcontrib>Choi, H-M.</creatorcontrib><creatorcontrib>Park, J-H.</creatorcontrib><creatorcontrib>Kim, E-C.</creatorcontrib><creatorcontrib>Choi, M-S.</creatorcontrib><creatorcontrib>An, H-J.</creatorcontrib><creatorcontrib>Um, J-Y.</creatorcontrib><creatorcontrib>Kim, H-M.</creatorcontrib><creatorcontrib>Min, B-I.</creatorcontrib><title>Inhibitory effects of Rumex japonicus Houtt. on the development of atopic dermatitis-like skin lesions in NC/Nga mice</title><title>British journal of dermatology (1951)</title><addtitle>Br J Dermatol</addtitle><description>Summary Background  Rumex japonicus Houtt. (RJH) is one of the herbs used in Eastern countries for the treatment of atopic dermatitis (AD). It has been shown to have an antioxidative effect in human skin disease. Objectives  To examine whether RJH extract (RJH‐E) suppresses the development of AD‐like skin lesions in NC/Nga mice, which are induced by the repeated application of picryl chloride (PC). Methods  The efficacy of RJH‐E in NC/Nga mice was assessed by measuring symptom severity, scratching behaviour, Staphylococcus aureus numbers on an ear, and serum levels of IgE, interleukin (IL)‐4 and interferon (IFN)‐γ. Results  Oral administration of RJH‐E to NC/Nga mice treated with PC inhibited the development of AD‐like skin lesions as exemplified by a significant decrease in total skin symptom severity scores, and a decrease in hypertrophy, hyperkeratosis and infiltration of inflammatory cells in the skin. The scratching behaviour and numbers of S. aureus, which are known to be exacerbated in AD, were also significantly reduced by RJH‐E. No significant change was observed in the serum levels of IFN‐γ, whereas IgE and IL‐4 levels were significantly reduced by RJH‐E. Conclusions  These results suggest that RJH‐E inhibits the development of AD‐like skin lesions in NC/Nga mice by suppressing the T‐helper 2 cell response. 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Stinging insect allergies</subject><subject>Staphylococcal Infections - complications</subject><subject>Staphylococcal Infections - drug therapy</subject><subject>Staphylococcus aureus - isolation &amp; purification</subject><subject>Treatment Outcome</subject><issn>0007-0963</issn><issn>1365-2133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkV1v2yAUhtG0aU27_YWJm-3OLhgM9sUutvQjrapUqrqPO0Tw8UpiG9fgLvn3w0vacsMR7_MiwYMQpiSlcZ2uU8pEnmSUsTQjRKREMsLS7Rs0ewneohkhRCakFOwIHXu_JoQykpP36IgKWWaSlzM0XnUPdmWDG3YY6hpM8NjV-G5sYYvXunedNaPHCzeGkGLX4fAAuIInaFzfQhcmWAfXWxNPh1YHG6xPGrsB7De2ww146zqP47icny7_aNxaAx_Qu1o3Hj4e9hP04-L8fr5Ibm4vr-bfbhLDCsGSihpWAaHCkAoKqbWgLCuqklWZZMD5KmY5Lw0nFDTPyrwq4osNLUtOpKyAnaAv-3v7wT2O4INqrTfQNLoDN3olilxImssIfjqA46qFSvWDbfWwU88fFYHPB0B7o5t60J2x_pWTBS8ynkXu6577axvYveZETeLUWk1-1ORHTeLUf3Fqq75fn01T7Cf7vvUBti99PWyUkEzm6tfyUt3d08XZ9U-ufrN_Rw6aZg</recordid><startdate>200607</startdate><enddate>200607</enddate><creator>Lee, H-S.</creator><creator>Kim, S-K.</creator><creator>Han, J-B.</creator><creator>Choi, H-M.</creator><creator>Park, J-H.</creator><creator>Kim, E-C.</creator><creator>Choi, M-S.</creator><creator>An, H-J.</creator><creator>Um, J-Y.</creator><creator>Kim, H-M.</creator><creator>Min, B-I.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200607</creationdate><title>Inhibitory effects of Rumex japonicus Houtt. on the development of atopic dermatitis-like skin lesions in NC/Nga mice</title><author>Lee, H-S. ; Kim, S-K. ; Han, J-B. ; Choi, H-M. ; Park, J-H. ; Kim, E-C. ; Choi, M-S. ; An, H-J. ; Um, J-Y. ; Kim, H-M. ; Min, B-I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3863-d1c3de016c0de87aa61328d93d273e44be01549c401ea4295d8007c1994077de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Allergic diseases</topic><topic>Animals</topic><topic>atopic dermatitis</topic><topic>Biological and medical sciences</topic><topic>Dermatitis, Atopic - drug therapy</topic><topic>Dermatitis, Atopic - immunology</topic><topic>Dermatitis, Atopic - microbiology</topic><topic>Dermatology</topic><topic>Female</topic><topic>IgE</topic><topic>Immunoglobulin E - blood</topic><topic>Immunopathology</topic><topic>Interferon-gamma - blood</topic><topic>interferon-γ</topic><topic>interleukin-4</topic><topic>Interleukin-4 - blood</topic><topic>Liver Function Tests</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Mutant Strains</topic><topic>Models, Animal</topic><topic>NC/Nga mice</topic><topic>Phytotherapy - methods</topic><topic>Picryl Chloride</topic><topic>Plant Extracts - therapeutic use</topic><topic>Plant Roots</topic><topic>Plants, Medicinal</topic><topic>Rumex</topic><topic>Rumex japonicus Houtt</topic><topic>Skin - drug effects</topic><topic>Skin allergic diseases. Stinging insect allergies</topic><topic>Staphylococcal Infections - complications</topic><topic>Staphylococcal Infections - drug therapy</topic><topic>Staphylococcus aureus - isolation &amp; purification</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, H-S.</creatorcontrib><creatorcontrib>Kim, S-K.</creatorcontrib><creatorcontrib>Han, J-B.</creatorcontrib><creatorcontrib>Choi, H-M.</creatorcontrib><creatorcontrib>Park, J-H.</creatorcontrib><creatorcontrib>Kim, E-C.</creatorcontrib><creatorcontrib>Choi, M-S.</creatorcontrib><creatorcontrib>An, H-J.</creatorcontrib><creatorcontrib>Um, J-Y.</creatorcontrib><creatorcontrib>Kim, H-M.</creatorcontrib><creatorcontrib>Min, B-I.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>British journal of dermatology (1951)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, H-S.</au><au>Kim, S-K.</au><au>Han, J-B.</au><au>Choi, H-M.</au><au>Park, J-H.</au><au>Kim, E-C.</au><au>Choi, M-S.</au><au>An, H-J.</au><au>Um, J-Y.</au><au>Kim, H-M.</au><au>Min, B-I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibitory effects of Rumex japonicus Houtt. on the development of atopic dermatitis-like skin lesions in NC/Nga mice</atitle><jtitle>British journal of dermatology (1951)</jtitle><addtitle>Br J Dermatol</addtitle><date>2006-07</date><risdate>2006</risdate><volume>155</volume><issue>1</issue><spage>33</spage><epage>38</epage><pages>33-38</pages><issn>0007-0963</issn><eissn>1365-2133</eissn><coden>BJDEAZ</coden><abstract>Summary Background  Rumex japonicus Houtt. (RJH) is one of the herbs used in Eastern countries for the treatment of atopic dermatitis (AD). It has been shown to have an antioxidative effect in human skin disease. Objectives  To examine whether RJH extract (RJH‐E) suppresses the development of AD‐like skin lesions in NC/Nga mice, which are induced by the repeated application of picryl chloride (PC). Methods  The efficacy of RJH‐E in NC/Nga mice was assessed by measuring symptom severity, scratching behaviour, Staphylococcus aureus numbers on an ear, and serum levels of IgE, interleukin (IL)‐4 and interferon (IFN)‐γ. Results  Oral administration of RJH‐E to NC/Nga mice treated with PC inhibited the development of AD‐like skin lesions as exemplified by a significant decrease in total skin symptom severity scores, and a decrease in hypertrophy, hyperkeratosis and infiltration of inflammatory cells in the skin. The scratching behaviour and numbers of S. aureus, which are known to be exacerbated in AD, were also significantly reduced by RJH‐E. No significant change was observed in the serum levels of IFN‐γ, whereas IgE and IL‐4 levels were significantly reduced by RJH‐E. Conclusions  These results suggest that RJH‐E inhibits the development of AD‐like skin lesions in NC/Nga mice by suppressing the T‐helper 2 cell response. Our results indicate that RJH treatment could provide an effective alternative therapy for the management of AD.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>16792749</pmid><doi>10.1111/j.1365-2133.2006.07303.x</doi><tpages>6</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Oxford University Press Journals All Titles (1996-Current)
subjects Allergic diseases
Animals
atopic dermatitis
Biological and medical sciences
Dermatitis, Atopic - drug therapy
Dermatitis, Atopic - immunology
Dermatitis, Atopic - microbiology
Dermatology
Female
IgE
Immunoglobulin E - blood
Immunopathology
Interferon-gamma - blood
interferon-γ
interleukin-4
Interleukin-4 - blood
Liver Function Tests
Medical sciences
Mice
Mice, Mutant Strains
Models, Animal
NC/Nga mice
Phytotherapy - methods
Picryl Chloride
Plant Extracts - therapeutic use
Plant Roots
Plants, Medicinal
Rumex
Rumex japonicus Houtt
Skin - drug effects
Skin allergic diseases. Stinging insect allergies
Staphylococcal Infections - complications
Staphylococcal Infections - drug therapy
Staphylococcus aureus - isolation & purification
Treatment Outcome
title Inhibitory effects of Rumex japonicus Houtt. on the development of atopic dermatitis-like skin lesions in NC/Nga mice
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