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Oleanolic acid acetate inhibits atopic dermatitis and allergic contact dermatitis in a murine model
Atopic dermatitis (AD) and allergic contact dermatitis (ACD) are common allergic and inflammatory skin diseases caused by a combination of eczema, scratching, pruritus, and cutaneous sensitization with allergens. This paper examines whether oleanolic acid acetate (OAA) modulates AD and ACD symptoms...
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Published in: | Toxicology and applied pharmacology 2013-05, Vol.269 (1), p.72-80 |
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description | Atopic dermatitis (AD) and allergic contact dermatitis (ACD) are common allergic and inflammatory skin diseases caused by a combination of eczema, scratching, pruritus, and cutaneous sensitization with allergens. This paper examines whether oleanolic acid acetate (OAA) modulates AD and ACD symptoms by using an existing AD model based on the repeated local exposure of mite extract (Dermatophagoides farinae extract, DFE) and 2,4-dinitrochlorobenzene to the ears of BALB/c mice. In addition, the paper uses a 2,4-dinitrofluorobenzene-sensitized local lymph node assay (LLNA) for the ACD model. The oral administration of OAA over a four-week period attenuated AD symptoms in terms of decreased skin lesions, epidermal thickness, the infiltration of immune cells (CD4+ cells, eosinophils, and mast cells), and serum IgE, IgG2a, and histamine levels. The gene expression of Th1, Th2, Th17, and Th22 cytokines was reduced by OAA in the lymph node and ear tissue, and the LLNA verified that OAA suppressed ACD. The oral administration of OAA over a three-day period attenuated ACD symptoms in terms of ear thickness, lymphocyte proliferation, and serum IgG2a levels. The gene expression of Th1, Th2, and Th17 cytokines was reduced by OAA in the thymus and ear tissue. Finally, to define the underlying mechanism, this paper uses a TNF-α/IFN-γ-activated human keratinocyte (HaCaT) model. OAA inhibited the expression of cytokines and chemokines through the downregulation of NF-κB and MAPKs in HaCaT cells. Taken together, the results indicate that OAA inhibited AD and ACD symptoms, suggesting that OAA may be effective in treating allergic skin disorders.
[Display omitted]
•OAA reduced both acute and chronic AD symptoms.•OAA had a controlling effect on the immune reaction for ACD.•The effect of OAA on allergic skin disorders was comparable to the cyclosporine A.•OAA might be a candidate for the treatment of allergic skin disorders. |
doi_str_mv | 10.1016/j.taap.2013.03.001 |
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[Display omitted]
•OAA reduced both acute and chronic AD symptoms.•OAA had a controlling effect on the immune reaction for ACD.•The effect of OAA on allergic skin disorders was comparable to the cyclosporine A.•OAA might be a candidate for the treatment of allergic skin disorders.</description><identifier>ISSN: 0041-008X</identifier><identifier>EISSN: 1096-0333</identifier><identifier>DOI: 10.1016/j.taap.2013.03.001</identifier><identifier>PMID: 23499868</identifier><identifier>CODEN: TXAPA9</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>60 APPLIED LIFE SCIENCES ; ACETATES ; Administration, Oral ; Allergic contact dermatitis ; Allergic diseases ; Animals ; Anti-Allergic Agents - administration & dosage ; Anti-Allergic Agents - pharmacology ; Antigens, Dermatophagoides ; Atopic dermatitis ; Biological and medical sciences ; Cell Line ; CYCLOSPORINE ; Cytokines - metabolism ; DERMATITIS ; Dermatitis, Allergic Contact - genetics ; Dermatitis, Allergic Contact - immunology ; Dermatitis, Allergic Contact - pathology ; Dermatitis, Allergic Contact - prevention & control ; Dermatitis, Atopic - genetics ; Dermatitis, Atopic - immunology ; Dermatitis, Atopic - pathology ; Dermatitis, Atopic - prevention & control ; Dinitrochlorobenzene ; Disease Models, Animal ; ECZEMA ; EOSINOPHILS ; Eosinophils - drug effects ; Eosinophils - immunology ; Female ; Gene Expression Regulation - drug effects ; Humans ; IMMUNE REACTIONS ; Immunopathology ; INFLAMMATION ; Inflammation Mediators - metabolism ; Keratinocyte ; Keratinocytes - drug effects ; Keratinocytes - immunology ; Local Lymph Node Assay ; LYMPH NODES ; LYMPHOKINES ; MAP Kinase Signaling System - drug effects ; MAST CELLS ; Mast Cells - drug effects ; Mast Cells - immunology ; Medical sciences ; MICE ; Mice, Inbred BALB C ; NF-kappa B - metabolism ; Oleanolic Acid - administration & dosage ; Oleanolic Acid - pharmacology ; Oleanolic acid acetate ; SKIN ; Skin - drug effects ; Skin - immunology ; Skin - pathology ; Skin allergic diseases. Stinging insect allergies ; T-Lymphocytes - drug effects ; T-Lymphocytes - immunology ; Time Factors ; Toxicology</subject><ispartof>Toxicology and applied pharmacology, 2013-05, Vol.269 (1), p.72-80</ispartof><rights>2013 Elsevier Inc.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-5d14751d1081eda1a71bbb22da8be5c9dde67962a9a77dcc8f4da49a39662ebb3</citedby><cites>FETCH-LOGICAL-c414t-5d14751d1081eda1a71bbb22da8be5c9dde67962a9a77dcc8f4da49a39662ebb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27358081$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23499868$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/22285298$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Choi, Jin Kyeong</creatorcontrib><creatorcontrib>Oh, Hyun-Mee</creatorcontrib><creatorcontrib>Lee, Soyoung</creatorcontrib><creatorcontrib>Park, Jin-Woo</creatorcontrib><creatorcontrib>Khang, Dongwoo</creatorcontrib><creatorcontrib>Lee, Seung Woong</creatorcontrib><creatorcontrib>Lee, Woo Song</creatorcontrib><creatorcontrib>Rho, Mun-Chual</creatorcontrib><creatorcontrib>Kim, Sang-Hyun</creatorcontrib><title>Oleanolic acid acetate inhibits atopic dermatitis and allergic contact dermatitis in a murine model</title><title>Toxicology and applied pharmacology</title><addtitle>Toxicol Appl Pharmacol</addtitle><description>Atopic dermatitis (AD) and allergic contact dermatitis (ACD) are common allergic and inflammatory skin diseases caused by a combination of eczema, scratching, pruritus, and cutaneous sensitization with allergens. This paper examines whether oleanolic acid acetate (OAA) modulates AD and ACD symptoms by using an existing AD model based on the repeated local exposure of mite extract (Dermatophagoides farinae extract, DFE) and 2,4-dinitrochlorobenzene to the ears of BALB/c mice. In addition, the paper uses a 2,4-dinitrofluorobenzene-sensitized local lymph node assay (LLNA) for the ACD model. The oral administration of OAA over a four-week period attenuated AD symptoms in terms of decreased skin lesions, epidermal thickness, the infiltration of immune cells (CD4+ cells, eosinophils, and mast cells), and serum IgE, IgG2a, and histamine levels. The gene expression of Th1, Th2, Th17, and Th22 cytokines was reduced by OAA in the lymph node and ear tissue, and the LLNA verified that OAA suppressed ACD. The oral administration of OAA over a three-day period attenuated ACD symptoms in terms of ear thickness, lymphocyte proliferation, and serum IgG2a levels. The gene expression of Th1, Th2, and Th17 cytokines was reduced by OAA in the thymus and ear tissue. Finally, to define the underlying mechanism, this paper uses a TNF-α/IFN-γ-activated human keratinocyte (HaCaT) model. OAA inhibited the expression of cytokines and chemokines through the downregulation of NF-κB and MAPKs in HaCaT cells. Taken together, the results indicate that OAA inhibited AD and ACD symptoms, suggesting that OAA may be effective in treating allergic skin disorders.
[Display omitted]
•OAA reduced both acute and chronic AD symptoms.•OAA had a controlling effect on the immune reaction for ACD.•The effect of OAA on allergic skin disorders was comparable to the cyclosporine A.•OAA might be a candidate for the treatment of allergic skin disorders.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>ACETATES</subject><subject>Administration, Oral</subject><subject>Allergic contact dermatitis</subject><subject>Allergic diseases</subject><subject>Animals</subject><subject>Anti-Allergic Agents - administration & dosage</subject><subject>Anti-Allergic Agents - pharmacology</subject><subject>Antigens, Dermatophagoides</subject><subject>Atopic dermatitis</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>CYCLOSPORINE</subject><subject>Cytokines - metabolism</subject><subject>DERMATITIS</subject><subject>Dermatitis, Allergic Contact - genetics</subject><subject>Dermatitis, Allergic Contact - immunology</subject><subject>Dermatitis, Allergic Contact - pathology</subject><subject>Dermatitis, Allergic Contact - prevention & control</subject><subject>Dermatitis, Atopic - genetics</subject><subject>Dermatitis, Atopic - immunology</subject><subject>Dermatitis, Atopic - pathology</subject><subject>Dermatitis, Atopic - prevention & control</subject><subject>Dinitrochlorobenzene</subject><subject>Disease Models, Animal</subject><subject>ECZEMA</subject><subject>EOSINOPHILS</subject><subject>Eosinophils - drug effects</subject><subject>Eosinophils - immunology</subject><subject>Female</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Humans</subject><subject>IMMUNE REACTIONS</subject><subject>Immunopathology</subject><subject>INFLAMMATION</subject><subject>Inflammation Mediators - metabolism</subject><subject>Keratinocyte</subject><subject>Keratinocytes - drug effects</subject><subject>Keratinocytes - immunology</subject><subject>Local Lymph Node Assay</subject><subject>LYMPH NODES</subject><subject>LYMPHOKINES</subject><subject>MAP Kinase Signaling System - drug effects</subject><subject>MAST CELLS</subject><subject>Mast Cells - drug effects</subject><subject>Mast Cells - immunology</subject><subject>Medical sciences</subject><subject>MICE</subject><subject>Mice, Inbred BALB C</subject><subject>NF-kappa B - metabolism</subject><subject>Oleanolic Acid - administration & dosage</subject><subject>Oleanolic Acid - pharmacology</subject><subject>Oleanolic acid acetate</subject><subject>SKIN</subject><subject>Skin - drug effects</subject><subject>Skin - immunology</subject><subject>Skin - pathology</subject><subject>Skin allergic diseases. Stinging insect allergies</subject><subject>T-Lymphocytes - drug effects</subject><subject>T-Lymphocytes - immunology</subject><subject>Time Factors</subject><subject>Toxicology</subject><issn>0041-008X</issn><issn>1096-0333</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kMFqHDEMhk1oSDabvEAPZaDkOBvZ45mxoZcS0rQQyKWF3IzG1iZeZjyL7QT69vGwadNTQUggfRK_fsY-cthw4N3VbpMR9xsBvNlACeBHbMVBdzU0TfOBrQAkrwHUwyk7S2kHAFpKfsJORSO1Vp1aMXs_EoZ59LZC611JlDFT5cOTH3xOFeZ5X4aO4oTZZ186oWDjSPGx9O0cMtr879yHCqvpOfpA1TQ7Gs_Z8RbHRBdvdc1-fbv5ef29vru__XH99a62kstct47LvuWOg-LkkGPPh2EQwqEaqLXaOep63QnU2PfOWrWVDqXGRnedoGFo1uzz4e6csjfJ-kz2qQgMZLMRQqhWaFUocaBsnFOKtDX76CeMvw0Hs_hqdmbx1Sy-GihR6pp9Oiztn4eJ3N-VP0YW4PINwGRx3EYM1qd3rm9aVf4q3JcDR8WIF09x0UnBkvNxkelm_z8drxmCl7c</recordid><startdate>20130515</startdate><enddate>20130515</enddate><creator>Choi, Jin Kyeong</creator><creator>Oh, Hyun-Mee</creator><creator>Lee, Soyoung</creator><creator>Park, Jin-Woo</creator><creator>Khang, Dongwoo</creator><creator>Lee, Seung Woong</creator><creator>Lee, Woo Song</creator><creator>Rho, Mun-Chual</creator><creator>Kim, Sang-Hyun</creator><general>Elsevier Inc</general><general>Elsevier</general><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>OTOTI</scope></search><sort><creationdate>20130515</creationdate><title>Oleanolic acid acetate inhibits atopic dermatitis and allergic contact dermatitis in a murine model</title><author>Choi, Jin Kyeong ; Oh, Hyun-Mee ; Lee, Soyoung ; Park, Jin-Woo ; Khang, Dongwoo ; Lee, Seung Woong ; Lee, Woo Song ; Rho, Mun-Chual ; Kim, Sang-Hyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-5d14751d1081eda1a71bbb22da8be5c9dde67962a9a77dcc8f4da49a39662ebb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>60 APPLIED LIFE SCIENCES</topic><topic>ACETATES</topic><topic>Administration, Oral</topic><topic>Allergic contact dermatitis</topic><topic>Allergic diseases</topic><topic>Animals</topic><topic>Anti-Allergic Agents - administration & dosage</topic><topic>Anti-Allergic Agents - pharmacology</topic><topic>Antigens, Dermatophagoides</topic><topic>Atopic dermatitis</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>CYCLOSPORINE</topic><topic>Cytokines - metabolism</topic><topic>DERMATITIS</topic><topic>Dermatitis, Allergic Contact - genetics</topic><topic>Dermatitis, Allergic Contact - immunology</topic><topic>Dermatitis, Allergic Contact - pathology</topic><topic>Dermatitis, Allergic Contact - prevention & control</topic><topic>Dermatitis, Atopic - genetics</topic><topic>Dermatitis, Atopic - immunology</topic><topic>Dermatitis, Atopic - pathology</topic><topic>Dermatitis, Atopic - prevention & control</topic><topic>Dinitrochlorobenzene</topic><topic>Disease Models, Animal</topic><topic>ECZEMA</topic><topic>EOSINOPHILS</topic><topic>Eosinophils - drug effects</topic><topic>Eosinophils - immunology</topic><topic>Female</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Humans</topic><topic>IMMUNE REACTIONS</topic><topic>Immunopathology</topic><topic>INFLAMMATION</topic><topic>Inflammation Mediators - metabolism</topic><topic>Keratinocyte</topic><topic>Keratinocytes - drug effects</topic><topic>Keratinocytes - immunology</topic><topic>Local Lymph Node Assay</topic><topic>LYMPH NODES</topic><topic>LYMPHOKINES</topic><topic>MAP Kinase Signaling System - drug effects</topic><topic>MAST CELLS</topic><topic>Mast Cells - drug effects</topic><topic>Mast Cells - immunology</topic><topic>Medical sciences</topic><topic>MICE</topic><topic>Mice, Inbred BALB C</topic><topic>NF-kappa B - metabolism</topic><topic>Oleanolic Acid - administration & dosage</topic><topic>Oleanolic Acid - pharmacology</topic><topic>Oleanolic acid acetate</topic><topic>SKIN</topic><topic>Skin - drug effects</topic><topic>Skin - immunology</topic><topic>Skin - pathology</topic><topic>Skin allergic diseases. Stinging insect allergies</topic><topic>T-Lymphocytes - drug effects</topic><topic>T-Lymphocytes - immunology</topic><topic>Time Factors</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choi, Jin Kyeong</creatorcontrib><creatorcontrib>Oh, Hyun-Mee</creatorcontrib><creatorcontrib>Lee, Soyoung</creatorcontrib><creatorcontrib>Park, Jin-Woo</creatorcontrib><creatorcontrib>Khang, Dongwoo</creatorcontrib><creatorcontrib>Lee, Seung Woong</creatorcontrib><creatorcontrib>Lee, Woo Song</creatorcontrib><creatorcontrib>Rho, Mun-Chual</creatorcontrib><creatorcontrib>Kim, Sang-Hyun</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Toxicology and applied pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choi, Jin Kyeong</au><au>Oh, Hyun-Mee</au><au>Lee, Soyoung</au><au>Park, Jin-Woo</au><au>Khang, Dongwoo</au><au>Lee, Seung Woong</au><au>Lee, Woo Song</au><au>Rho, Mun-Chual</au><au>Kim, Sang-Hyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oleanolic acid acetate inhibits atopic dermatitis and allergic contact dermatitis in a murine model</atitle><jtitle>Toxicology and applied pharmacology</jtitle><addtitle>Toxicol Appl Pharmacol</addtitle><date>2013-05-15</date><risdate>2013</risdate><volume>269</volume><issue>1</issue><spage>72</spage><epage>80</epage><pages>72-80</pages><issn>0041-008X</issn><eissn>1096-0333</eissn><coden>TXAPA9</coden><abstract>Atopic dermatitis (AD) and allergic contact dermatitis (ACD) are common allergic and inflammatory skin diseases caused by a combination of eczema, scratching, pruritus, and cutaneous sensitization with allergens. This paper examines whether oleanolic acid acetate (OAA) modulates AD and ACD symptoms by using an existing AD model based on the repeated local exposure of mite extract (Dermatophagoides farinae extract, DFE) and 2,4-dinitrochlorobenzene to the ears of BALB/c mice. In addition, the paper uses a 2,4-dinitrofluorobenzene-sensitized local lymph node assay (LLNA) for the ACD model. The oral administration of OAA over a four-week period attenuated AD symptoms in terms of decreased skin lesions, epidermal thickness, the infiltration of immune cells (CD4+ cells, eosinophils, and mast cells), and serum IgE, IgG2a, and histamine levels. The gene expression of Th1, Th2, Th17, and Th22 cytokines was reduced by OAA in the lymph node and ear tissue, and the LLNA verified that OAA suppressed ACD. The oral administration of OAA over a three-day period attenuated ACD symptoms in terms of ear thickness, lymphocyte proliferation, and serum IgG2a levels. The gene expression of Th1, Th2, and Th17 cytokines was reduced by OAA in the thymus and ear tissue. Finally, to define the underlying mechanism, this paper uses a TNF-α/IFN-γ-activated human keratinocyte (HaCaT) model. OAA inhibited the expression of cytokines and chemokines through the downregulation of NF-κB and MAPKs in HaCaT cells. Taken together, the results indicate that OAA inhibited AD and ACD symptoms, suggesting that OAA may be effective in treating allergic skin disorders.
[Display omitted]
•OAA reduced both acute and chronic AD symptoms.•OAA had a controlling effect on the immune reaction for ACD.•The effect of OAA on allergic skin disorders was comparable to the cyclosporine A.•OAA might be a candidate for the treatment of allergic skin disorders.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>23499868</pmid><doi>10.1016/j.taap.2013.03.001</doi><tpages>9</tpages></addata></record> |
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subjects | 60 APPLIED LIFE SCIENCES ACETATES Administration, Oral Allergic contact dermatitis Allergic diseases Animals Anti-Allergic Agents - administration & dosage Anti-Allergic Agents - pharmacology Antigens, Dermatophagoides Atopic dermatitis Biological and medical sciences Cell Line CYCLOSPORINE Cytokines - metabolism DERMATITIS Dermatitis, Allergic Contact - genetics Dermatitis, Allergic Contact - immunology Dermatitis, Allergic Contact - pathology Dermatitis, Allergic Contact - prevention & control Dermatitis, Atopic - genetics Dermatitis, Atopic - immunology Dermatitis, Atopic - pathology Dermatitis, Atopic - prevention & control Dinitrochlorobenzene Disease Models, Animal ECZEMA EOSINOPHILS Eosinophils - drug effects Eosinophils - immunology Female Gene Expression Regulation - drug effects Humans IMMUNE REACTIONS Immunopathology INFLAMMATION Inflammation Mediators - metabolism Keratinocyte Keratinocytes - drug effects Keratinocytes - immunology Local Lymph Node Assay LYMPH NODES LYMPHOKINES MAP Kinase Signaling System - drug effects MAST CELLS Mast Cells - drug effects Mast Cells - immunology Medical sciences MICE Mice, Inbred BALB C NF-kappa B - metabolism Oleanolic Acid - administration & dosage Oleanolic Acid - pharmacology Oleanolic acid acetate SKIN Skin - drug effects Skin - immunology Skin - pathology Skin allergic diseases. Stinging insect allergies T-Lymphocytes - drug effects T-Lymphocytes - immunology Time Factors Toxicology |
title | Oleanolic acid acetate inhibits atopic dermatitis and allergic contact dermatitis in a murine model |
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