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...

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Main Authors: Imane Bouakkaz, Kamel Khelili, Tarek Rebai, Andreas Lock
Format: Article
Language:English
Published: SAGE Publishing 2018-10-01
Series:Dose-Response
Online Access:https://doi.org/10.1177/1559325818799560
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spelling doaj-4cec1f36f04e4cfd8017b6ed3fe2e0bd2020-11-25T03:19:16ZengSAGE PublishingDose-Response1559-32582018-10-011610.1177/1559325818799560Pulmonary Toxicity Induced by N-Hexane in Wistar Male Rats After Oral Subchronic ExposureImane Bouakkaz0Kamel Khelili1Tarek Rebai2Andreas Lock3 Animal Ecophysiology Laboratory, Faculty of Sciences, Badji Mokhtar University, Annaba, Algeria Animal Ecophysiology Laboratory, Faculty of Sciences, Badji Mokhtar University, Annaba, Algeria Histology-Embryology Laboratory, Sfax Medicine College, Sfax, Tunisia Althisia-Histology Laboratory, Troyes, FranceStudies 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.https://doi.org/10.1177/1559325818799560
collection DOAJ
language English
format Article
sources DOAJ
author Imane Bouakkaz
Kamel Khelili
Tarek Rebai
Andreas Lock
spellingShingle Imane Bouakkaz
Kamel Khelili
Tarek Rebai
Andreas Lock
Pulmonary Toxicity Induced by N-Hexane in Wistar Male Rats After Oral Subchronic Exposure
Dose-Response
author_facet Imane Bouakkaz
Kamel Khelili
Tarek Rebai
Andreas Lock
author_sort Imane Bouakkaz
title 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_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_sort pulmonary toxicity induced by n-hexane in wistar male rats after oral subchronic exposure
publisher SAGE Publishing
series Dose-Response
issn 1559-3258
publishDate 2018-10-01
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.
url https://doi.org/10.1177/1559325818799560
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AT kamelkhelili pulmonarytoxicityinducedbynhexaneinwistarmaleratsafteroralsubchronicexposure
AT tarekrebai pulmonarytoxicityinducedbynhexaneinwistarmaleratsafteroralsubchronicexposure
AT andreaslock pulmonarytoxicityinducedbynhexaneinwistarmaleratsafteroralsubchronicexposure
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