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Comparison of Biological Responses in Rats Under Various Cigarette Smoke Exposure Conditions
A variety of exposure regimens of cigarette smoke have been used in animal models of lung diseases. In this study, we compared biological responses of smoke exposure in rats, using different smoke concentrations (wet total particulate matter [WTPM]), daily exposure durations, and total days of expos...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Society of Toxicologic Pathology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695338/ https://www.ncbi.nlm.nih.gov/pubmed/23914058 http://dx.doi.org/10.1293/tox.26.159 |
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author | Tsuji, Hiroyuki Fujimoto, Hitoshi Matsuura, Daiki Nishino, Tomoki Lee, K Monica Yoshimura, Hiroyuki |
author_facet | Tsuji, Hiroyuki Fujimoto, Hitoshi Matsuura, Daiki Nishino, Tomoki Lee, K Monica Yoshimura, Hiroyuki |
author_sort | Tsuji, Hiroyuki |
collection | PubMed |
description | A variety of exposure regimens of cigarette smoke have been used in animal models of lung diseases. In this study, we compared biological responses of smoke exposure in rats, using different smoke concentrations (wet total particulate matter [WTPM]), daily exposure durations, and total days of exposure. As a range-finding acute study, we first compared pulmonary responses between SD and F344 strains after a single nose-only exposure to mainstream cigarette smoke or LPS. Secondly, F344 rats were exposed to cigarette smoke for 2 or 13 weeks under the comparable daily exposure dose (WTPM concentration x daily exposure duration; according to Haber’s rule) but at a different WTPM concentration or daily exposure duration. Blood carboxylhemoglobin was increased linearly to the WTPM concentration, while urinary nicotine plus cotinine value was higher for the longer daily exposure than the corresponding shorter exposure groups. Gamma glutamyl transferase activity in bronchoalveolar lavage fluid (BALF) was increased dose dependently after 2 and 13 weeks of cigarette smoke exposure, while the neutrophil content in BALF was not increased notably. Smoke-exposed groups showed reduced body weight gain and increased relative lung and heart weights. While BALF parameters and the relative lung weights suggest pulmonary responses, histopathological examination showed epithelial lesions mainly in the upper respiratory organs (nose and larynx). Collectively, the results indicate that, under the employed study design, the equivalent daily exposure dose (exposure concentration x duration) induces equivalent pulmonary responses in rats. |
format | Online Article Text |
id | pubmed-3695338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Japanese Society of Toxicologic Pathology |
record_format | MEDLINE/PubMed |
spelling | pubmed-36953382013-08-02 Comparison of Biological Responses in Rats Under Various Cigarette Smoke Exposure Conditions Tsuji, Hiroyuki Fujimoto, Hitoshi Matsuura, Daiki Nishino, Tomoki Lee, K Monica Yoshimura, Hiroyuki J Toxicol Pathol Original Article A variety of exposure regimens of cigarette smoke have been used in animal models of lung diseases. In this study, we compared biological responses of smoke exposure in rats, using different smoke concentrations (wet total particulate matter [WTPM]), daily exposure durations, and total days of exposure. As a range-finding acute study, we first compared pulmonary responses between SD and F344 strains after a single nose-only exposure to mainstream cigarette smoke or LPS. Secondly, F344 rats were exposed to cigarette smoke for 2 or 13 weeks under the comparable daily exposure dose (WTPM concentration x daily exposure duration; according to Haber’s rule) but at a different WTPM concentration or daily exposure duration. Blood carboxylhemoglobin was increased linearly to the WTPM concentration, while urinary nicotine plus cotinine value was higher for the longer daily exposure than the corresponding shorter exposure groups. Gamma glutamyl transferase activity in bronchoalveolar lavage fluid (BALF) was increased dose dependently after 2 and 13 weeks of cigarette smoke exposure, while the neutrophil content in BALF was not increased notably. Smoke-exposed groups showed reduced body weight gain and increased relative lung and heart weights. While BALF parameters and the relative lung weights suggest pulmonary responses, histopathological examination showed epithelial lesions mainly in the upper respiratory organs (nose and larynx). Collectively, the results indicate that, under the employed study design, the equivalent daily exposure dose (exposure concentration x duration) induces equivalent pulmonary responses in rats. Japanese Society of Toxicologic Pathology 2013-07-10 2013-06 /pmc/articles/PMC3695338/ /pubmed/23914058 http://dx.doi.org/10.1293/tox.26.159 Text en ©2013 The Japanese Society of Toxicologic Pathology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Original Article Tsuji, Hiroyuki Fujimoto, Hitoshi Matsuura, Daiki Nishino, Tomoki Lee, K Monica Yoshimura, Hiroyuki Comparison of Biological Responses in Rats Under Various Cigarette Smoke Exposure Conditions |
title | Comparison of Biological Responses in Rats Under Various Cigarette Smoke Exposure Conditions |
title_full | Comparison of Biological Responses in Rats Under Various Cigarette Smoke Exposure Conditions |
title_fullStr | Comparison of Biological Responses in Rats Under Various Cigarette Smoke Exposure Conditions |
title_full_unstemmed | Comparison of Biological Responses in Rats Under Various Cigarette Smoke Exposure Conditions |
title_short | Comparison of Biological Responses in Rats Under Various Cigarette Smoke Exposure Conditions |
title_sort | comparison of biological responses in rats under various cigarette smoke exposure conditions |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695338/ https://www.ncbi.nlm.nih.gov/pubmed/23914058 http://dx.doi.org/10.1293/tox.26.159 |
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