Abstract | BACKGROUND: METHODS:
DEP were extracted with benzene/ ethanol, and the soluble organic fraction formed the DEP-OC. NC/Nga male mice received simultaneous application of DEP-OC and/or PiCl on their ears once a week for 9 or 3 weeks. We evaluated skin lesions by noting scaling, eruption, excoriation, erosion, hemorrhage, pathologic changes, production of cytokines, and IgE level in the serum. RESULTS:
PiCl application alone produced progressively severe AD-like skin lesions. The application of PiCl plus DEP-OC resulted in a marked worsening of skin lesions in the early stages of AD. Moreover, mast cell counts significantly increased in the subcutaneous tissue. Administration of PiCl combined with DEP-OC resulted in a greater increase in the local expression of interleukin-4, keratinocyte chemoattractant, and neutrophils in subcutaneous tissue compared with PiCl treatment alone. In contrast, the combination treatment produced lower levels of IFN-γ compared with PiCl treatment alone. CONCLUSIONS:
DEP-OC application to the skin aggravated PiCl-induced AD. This aggravation may be due to activation of the Th2-associated immune responses by the organic chemicals in DEP.
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Authors | Kaori Sadakane, Takamichi Ichinose, Hirohisa Takano, Rie Yanagisawa, Ken-ichiro Inoue, Hiroaki Kawazato, Aiko Yasuda, Kazuichi Hayakawa |
Journal | International archives of allergy and immunology
(Int Arch Allergy Immunol)
Vol. 162
Issue 1
Pg. 7-15
( 2013)
ISSN: 1423-0097 [Electronic] Switzerland |
PMID | 23817207
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2013 S. Karger AG, Basel. |
Chemical References |
- Organic Chemicals
- Vehicle Emissions
- Picryl Chloride
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Topics |
- Animals
- Dermatitis, Atopic
(chemically induced, immunology, physiopathology)
- Disease Models, Animal
- Gene Expression Regulation
(drug effects)
- Male
- Mast Cells
(drug effects)
- Mice
- Organic Chemicals
(toxicity)
- Picryl Chloride
- Skin
(drug effects)
- Vehicle Emissions
(analysis, toxicity)
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