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Trichloroethylene and trichloroethanol induce skin sensitization with focal hepatic necrosis in guinea pigs

OBJECTIVES: Occupational exposure to trichloroethylene (TCE) induces trichloroethylene hypersensitivity syndrome (TCEHS), which causes hypersensitivity dermatitis and hepatitis. However, whether TCE itself or its two metabolites, trichloroethanol (TCEOH) and trichloroacetic acid (TCA), are involved...

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Autores principales: Zhao, Na, Song, Xiangrong, Naito, Hisao, Li, Hongling, Huang, Yongshun, Liu, Lili, Lu, Fengrong, Cai, Tingfeng, Ito, Yuki, Kamijima, Michihiro, Huang, Hanlin, Nakajima, Tamie, Wang, Hailan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428806/
https://www.ncbi.nlm.nih.gov/pubmed/32799435
http://dx.doi.org/10.1002/1348-9585.12142
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author Zhao, Na
Song, Xiangrong
Naito, Hisao
Li, Hongling
Huang, Yongshun
Liu, Lili
Lu, Fengrong
Cai, Tingfeng
Ito, Yuki
Kamijima, Michihiro
Huang, Hanlin
Nakajima, Tamie
Wang, Hailan
author_facet Zhao, Na
Song, Xiangrong
Naito, Hisao
Li, Hongling
Huang, Yongshun
Liu, Lili
Lu, Fengrong
Cai, Tingfeng
Ito, Yuki
Kamijima, Michihiro
Huang, Hanlin
Nakajima, Tamie
Wang, Hailan
author_sort Zhao, Na
collection PubMed
description OBJECTIVES: Occupational exposure to trichloroethylene (TCE) induces trichloroethylene hypersensitivity syndrome (TCEHS), which causes hypersensitivity dermatitis and hepatitis. However, whether TCE itself or its two metabolites, trichloroethanol (TCEOH) and trichloroacetic acid (TCA), are involved in TCEHS remains unclear. Therefore, in this study we explored the allergens causing TCEHS and characterized TCEHS‐related liver injury in guinea pigs. METHOD: The guinea pig maximization test was performed using TCE, TCEOH, and TCA as candidate allergens. Skin inflammation was scored, and liver function and histopathological changes were evaluated by biochemical tests and hematoxylin and eosin staining, respectively. RESULTS: The sensitization rates for TCE, TCEOH, and TCA were 90.0%, 50.0%, and 0.0%, respectively. In the TCE and TCEOH experimental groups, the skin showed varying degrees of erythema with eosinophil granulocyte infiltration in the dermis. Additionally, serum alanine aminotransferase and γ‐glutamyl transpeptidase levels increased significantly, and histological analysis revealed focal hepatocellular necrosis with inflammatory cell infiltration in the liver. CONCLUSIONS: TCE is the main cause of allergy and TCEOH is a secondary factor for allergy in guinea pigs. TCE and TCEOH can cause immune‐mediated skin sensitization complicated by focal hepatic necrosis.
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spelling pubmed-74288062020-08-18 Trichloroethylene and trichloroethanol induce skin sensitization with focal hepatic necrosis in guinea pigs Zhao, Na Song, Xiangrong Naito, Hisao Li, Hongling Huang, Yongshun Liu, Lili Lu, Fengrong Cai, Tingfeng Ito, Yuki Kamijima, Michihiro Huang, Hanlin Nakajima, Tamie Wang, Hailan J Occup Health Original Articles OBJECTIVES: Occupational exposure to trichloroethylene (TCE) induces trichloroethylene hypersensitivity syndrome (TCEHS), which causes hypersensitivity dermatitis and hepatitis. However, whether TCE itself or its two metabolites, trichloroethanol (TCEOH) and trichloroacetic acid (TCA), are involved in TCEHS remains unclear. Therefore, in this study we explored the allergens causing TCEHS and characterized TCEHS‐related liver injury in guinea pigs. METHOD: The guinea pig maximization test was performed using TCE, TCEOH, and TCA as candidate allergens. Skin inflammation was scored, and liver function and histopathological changes were evaluated by biochemical tests and hematoxylin and eosin staining, respectively. RESULTS: The sensitization rates for TCE, TCEOH, and TCA were 90.0%, 50.0%, and 0.0%, respectively. In the TCE and TCEOH experimental groups, the skin showed varying degrees of erythema with eosinophil granulocyte infiltration in the dermis. Additionally, serum alanine aminotransferase and γ‐glutamyl transpeptidase levels increased significantly, and histological analysis revealed focal hepatocellular necrosis with inflammatory cell infiltration in the liver. CONCLUSIONS: TCE is the main cause of allergy and TCEOH is a secondary factor for allergy in guinea pigs. TCE and TCEOH can cause immune‐mediated skin sensitization complicated by focal hepatic necrosis. John Wiley and Sons Inc. 2020-08-15 /pmc/articles/PMC7428806/ /pubmed/32799435 http://dx.doi.org/10.1002/1348-9585.12142 Text en © 2020 The Authors. Journal of Occupational Health published by John Wiley & Sons Australia, Ltd on behalf of The Japan Society for Occupational Health This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Zhao, Na
Song, Xiangrong
Naito, Hisao
Li, Hongling
Huang, Yongshun
Liu, Lili
Lu, Fengrong
Cai, Tingfeng
Ito, Yuki
Kamijima, Michihiro
Huang, Hanlin
Nakajima, Tamie
Wang, Hailan
Trichloroethylene and trichloroethanol induce skin sensitization with focal hepatic necrosis in guinea pigs
title Trichloroethylene and trichloroethanol induce skin sensitization with focal hepatic necrosis in guinea pigs
title_full Trichloroethylene and trichloroethanol induce skin sensitization with focal hepatic necrosis in guinea pigs
title_fullStr Trichloroethylene and trichloroethanol induce skin sensitization with focal hepatic necrosis in guinea pigs
title_full_unstemmed Trichloroethylene and trichloroethanol induce skin sensitization with focal hepatic necrosis in guinea pigs
title_short Trichloroethylene and trichloroethanol induce skin sensitization with focal hepatic necrosis in guinea pigs
title_sort trichloroethylene and trichloroethanol induce skin sensitization with focal hepatic necrosis in guinea pigs
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428806/
https://www.ncbi.nlm.nih.gov/pubmed/32799435
http://dx.doi.org/10.1002/1348-9585.12142
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