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Pulmonary Toxicity Induced by N-Hexane in Wistar Male Rats After Oral Subchronic Exposure
Studies of pulmonary toxicity induced by oral exposure to n-hexane are very few, in contrast to those studying the exposure by inhalation. This research tackles the oral toxic effect of n-hexane solvent on the lungs after subchronic exposure of Wistar male rats at 300, 600, and 1200 mg/kg, respectiv...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194936/ https://www.ncbi.nlm.nih.gov/pubmed/30349425 http://dx.doi.org/10.1177/1559325818799560 |
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author | Bouakkaz, Imène Khelili, Kamel Rebai, Tarek Lock, Andreas |
author_facet | Bouakkaz, Imène Khelili, Kamel Rebai, Tarek Lock, Andreas |
author_sort | Bouakkaz, Imène |
collection | PubMed |
description | Studies of pulmonary toxicity induced by oral exposure to n-hexane are very few, in contrast to those studying the exposure by inhalation. This research tackles the oral toxic effect of n-hexane solvent on the lungs after subchronic exposure of Wistar male rats at 300, 600, and 1200 mg/kg, respectively, each day for 8 weeks. The pneumotoxicity observed in this study was marked by an immune toxicity in the form of a significant increase in the levels of white blood cells, lymphocytes, granulocytes, and eosinophils, as well as a significant increase in relative and absolute lung weight in both groups treated at the doses of 600 and 1200 mg/kg. n-Hexane also resulted in a significant increase in serum total proteins and acid phosphatase in the 3 doses tested daily for 8 weeks. In addition, we found a significant increase in total protein and a decrease in glutathione at 600 and 1200 mg/kg, in the pulmonary homogenate. Furthermore, the rate of lipid peroxidation increased in the 3 doses tested. Histological findings revealed a pneumonia characterized by bronchopneumonia, fibronecrotic lesions, congestion, hemorrhage, type II pneumocyte hyperplasia, alveolar lesions, bronchial epithelium degradation, and inflammation. |
format | Online Article Text |
id | pubmed-6194936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-61949362018-10-22 Pulmonary Toxicity Induced by N-Hexane in Wistar Male Rats After Oral Subchronic Exposure Bouakkaz, Imène Khelili, Kamel Rebai, Tarek Lock, Andreas Dose Response Original Article Studies of pulmonary toxicity induced by oral exposure to n-hexane are very few, in contrast to those studying the exposure by inhalation. This research tackles the oral toxic effect of n-hexane solvent on the lungs after subchronic exposure of Wistar male rats at 300, 600, and 1200 mg/kg, respectively, each day for 8 weeks. The pneumotoxicity observed in this study was marked by an immune toxicity in the form of a significant increase in the levels of white blood cells, lymphocytes, granulocytes, and eosinophils, as well as a significant increase in relative and absolute lung weight in both groups treated at the doses of 600 and 1200 mg/kg. n-Hexane also resulted in a significant increase in serum total proteins and acid phosphatase in the 3 doses tested daily for 8 weeks. In addition, we found a significant increase in total protein and a decrease in glutathione at 600 and 1200 mg/kg, in the pulmonary homogenate. Furthermore, the rate of lipid peroxidation increased in the 3 doses tested. Histological findings revealed a pneumonia characterized by bronchopneumonia, fibronecrotic lesions, congestion, hemorrhage, type II pneumocyte hyperplasia, alveolar lesions, bronchial epithelium degradation, and inflammation. SAGE Publications 2018-10-15 /pmc/articles/PMC6194936/ /pubmed/30349425 http://dx.doi.org/10.1177/1559325818799560 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Bouakkaz, Imène Khelili, Kamel Rebai, Tarek Lock, Andreas Pulmonary Toxicity Induced by N-Hexane in Wistar Male Rats After Oral Subchronic Exposure |
title | Pulmonary Toxicity Induced by N-Hexane in Wistar Male Rats After Oral Subchronic Exposure |
title_full | Pulmonary Toxicity Induced by N-Hexane in Wistar Male Rats After Oral Subchronic Exposure |
title_fullStr | Pulmonary Toxicity Induced by N-Hexane in Wistar Male Rats After Oral Subchronic Exposure |
title_full_unstemmed | Pulmonary Toxicity Induced by N-Hexane in Wistar Male Rats After Oral Subchronic Exposure |
title_short | Pulmonary Toxicity Induced by N-Hexane in Wistar Male Rats After Oral Subchronic Exposure |
title_sort | pulmonary toxicity induced by n-hexane in wistar male rats after oral subchronic exposure |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194936/ https://www.ncbi.nlm.nih.gov/pubmed/30349425 http://dx.doi.org/10.1177/1559325818799560 |
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