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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c414t-5d14751d1081eda1a71bbb22da8be5c9dde67962a9a77dcc8f4da49a39662ebb3
cites cdi_FETCH-LOGICAL-c414t-5d14751d1081eda1a71bbb22da8be5c9dde67962a9a77dcc8f4da49a39662ebb3
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container_title Toxicology and applied pharmacology
container_volume 269
creator 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
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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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><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 &amp; 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 &amp; control ; Dermatitis, Atopic - genetics ; Dermatitis, Atopic - immunology ; Dermatitis, Atopic - pathology ; Dermatitis, Atopic - prevention &amp; 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 &amp; dosage ; Oleanolic Acid - pharmacology ; Oleanolic acid acetate ; SKIN ; Skin - drug effects ; Skin - immunology ; Skin - pathology ; Skin allergic diseases. 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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 &amp; 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 &amp; control</subject><subject>Dermatitis, Atopic - genetics</subject><subject>Dermatitis, Atopic - immunology</subject><subject>Dermatitis, Atopic - pathology</subject><subject>Dermatitis, Atopic - prevention &amp; 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 &amp; 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. 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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. 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ispartof Toxicology and applied pharmacology, 2013-05, Vol.269 (1), p.72-80
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1096-0333
language eng
recordid cdi_osti_scitechconnect_22285298
source Elsevier
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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