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Di-(2-ethylhexyl) Phthalate Enhances Atopic Dermatitis-Like Skin Lesions in Mice
Di-(2-ethylhexyl) phthalate (DEHP) has been widely used in polyvinyl chloride products and has become ubiquitous in the developed countries. DEHP reportedly displays an adjuvant effect on immunoglobulin production. However, it has not been elucidated whether DEHP is associated with the aggravation o...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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National Institute of Environmental Health Sciences
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1552025/ https://www.ncbi.nlm.nih.gov/pubmed/16882537 http://dx.doi.org/10.1289/ehp.8985 |
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author | Takano, Hirohisa Yanagisawa, Rie Inoue, Ken-ichiro Ichinose, Takamichi Sadakane, Kaori Yoshikawa, Toshikazu |
author_facet | Takano, Hirohisa Yanagisawa, Rie Inoue, Ken-ichiro Ichinose, Takamichi Sadakane, Kaori Yoshikawa, Toshikazu |
author_sort | Takano, Hirohisa |
collection | PubMed |
description | Di-(2-ethylhexyl) phthalate (DEHP) has been widely used in polyvinyl chloride products and has become ubiquitous in the developed countries. DEHP reportedly displays an adjuvant effect on immunoglobulin production. However, it has not been elucidated whether DEHP is associated with the aggravation of atopic dermatitis. We investigated the effects of DEHP on atopic dermatitis-like skin lesions induced by mite allergen in NC/Nga mice. NC/Nga male mice were injected intradermally with mite allergen on their right ears. In the presence of allergen, DEHP (0, 0.8, 4, 20, or 100 μg) was administered by intraperitoneal injection. We evaluated clinical scores, ear thickening, histologic findings, and the protein expression of chemokines. Exposure to DEHP at a dose of 0.8–20 μg caused deterioration of atopic dermatitis-like skin lesions related to mite allergen; this was evident from macroscopic and microscopic examinations. Furthermore, these changes were consistent with the protein expression of proinflammatory molecules such as macrophage inflammatory protein-1α (MIP-1α) and eotaxin in the ear tissue in overall trend. In contrast, 100 μg DEHP did not show the enhancing effects. These results indicate that DEHP enhances atopic dermatitis-like skin lesions at hundred-fold lower levels than the no observed adverse effect level determined on histologic changes in the liver of rodents. DEHP could be at least partly responsible for the recent increase in atopic dermatitis. |
format | Text |
id | pubmed-1552025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | National Institute of Environmental Health Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-15520252006-08-29 Di-(2-ethylhexyl) Phthalate Enhances Atopic Dermatitis-Like Skin Lesions in Mice Takano, Hirohisa Yanagisawa, Rie Inoue, Ken-ichiro Ichinose, Takamichi Sadakane, Kaori Yoshikawa, Toshikazu Environ Health Perspect Research Di-(2-ethylhexyl) phthalate (DEHP) has been widely used in polyvinyl chloride products and has become ubiquitous in the developed countries. DEHP reportedly displays an adjuvant effect on immunoglobulin production. However, it has not been elucidated whether DEHP is associated with the aggravation of atopic dermatitis. We investigated the effects of DEHP on atopic dermatitis-like skin lesions induced by mite allergen in NC/Nga mice. NC/Nga male mice were injected intradermally with mite allergen on their right ears. In the presence of allergen, DEHP (0, 0.8, 4, 20, or 100 μg) was administered by intraperitoneal injection. We evaluated clinical scores, ear thickening, histologic findings, and the protein expression of chemokines. Exposure to DEHP at a dose of 0.8–20 μg caused deterioration of atopic dermatitis-like skin lesions related to mite allergen; this was evident from macroscopic and microscopic examinations. Furthermore, these changes were consistent with the protein expression of proinflammatory molecules such as macrophage inflammatory protein-1α (MIP-1α) and eotaxin in the ear tissue in overall trend. In contrast, 100 μg DEHP did not show the enhancing effects. These results indicate that DEHP enhances atopic dermatitis-like skin lesions at hundred-fold lower levels than the no observed adverse effect level determined on histologic changes in the liver of rodents. DEHP could be at least partly responsible for the recent increase in atopic dermatitis. National Institute of Environmental Health Sciences 2006-08 2006-05-15 /pmc/articles/PMC1552025/ /pubmed/16882537 http://dx.doi.org/10.1289/ehp.8985 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, ?Reproduced with permission from Environmental Health Perspectives?); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright. |
spellingShingle | Research Takano, Hirohisa Yanagisawa, Rie Inoue, Ken-ichiro Ichinose, Takamichi Sadakane, Kaori Yoshikawa, Toshikazu Di-(2-ethylhexyl) Phthalate Enhances Atopic Dermatitis-Like Skin Lesions in Mice |
title | Di-(2-ethylhexyl) Phthalate Enhances Atopic Dermatitis-Like Skin Lesions
in Mice |
title_full | Di-(2-ethylhexyl) Phthalate Enhances Atopic Dermatitis-Like Skin Lesions
in Mice |
title_fullStr | Di-(2-ethylhexyl) Phthalate Enhances Atopic Dermatitis-Like Skin Lesions
in Mice |
title_full_unstemmed | Di-(2-ethylhexyl) Phthalate Enhances Atopic Dermatitis-Like Skin Lesions
in Mice |
title_short | Di-(2-ethylhexyl) Phthalate Enhances Atopic Dermatitis-Like Skin Lesions
in Mice |
title_sort | di-(2-ethylhexyl) phthalate enhances atopic dermatitis-like skin lesions
in mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1552025/ https://www.ncbi.nlm.nih.gov/pubmed/16882537 http://dx.doi.org/10.1289/ehp.8985 |
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