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A germ-free status does not protect from the lethal effects of acute lung damage caused by o,s,s,-trimethyl phosphorodithioate
To investigate whether a normal resident microbiological flora of conventional rats influences the lethality of chemical-induced lung damage, the pneumotoxin O,S,S-trimethyl phosphorodithioate (OSSMe, 75 or 100 mg/kg, s.c.) was administered to age-matched conventional and germ-free male F344 rats. M...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Ireland Ltd.
1986
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131465/ https://www.ncbi.nlm.nih.gov/pubmed/3738927 http://dx.doi.org/10.1016/0378-4274(86)90062-7 |
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author | Nemery, B. Tucker, D.K. Sparrow, S. |
author_facet | Nemery, B. Tucker, D.K. Sparrow, S. |
author_sort | Nemery, B. |
collection | PubMed |
description | To investigate whether a normal resident microbiological flora of conventional rats influences the lethality of chemical-induced lung damage, the pneumotoxin O,S,S-trimethyl phosphorodithioate (OSSMe, 75 or 100 mg/kg, s.c.) was administered to age-matched conventional and germ-free male F344 rats. Microbiological and serological examinations confirmed the germ-free state of the germ-free rats and showed that no specific lung pathogens were present in the conventional rats. As in conventional rats, clinical symptoms and death of OSSMe-treated germ-free rats resulted from respiratory failure. The germ-free rats were not more resistant, but rather more susceptible to OSSMe than conventional rats. Increases in lung weight and histological examination of lung tissue 3 days after dosing with OSSMe (75 mg/kg, s.c.) showed no differences between germ-free and conventional rats. Despite alterations in their nasopharyngeal flora, death in the conventional rats was probably not caused by bacterial superinfection. The higher susceptibility of germ-free rats to OSSMe can be partly attributed to pharmacokinetic differences, since plasma levels of OSSMe decreased more slowly in germ-free than in conventional rats. It is concluded that germ-free rats are not protected from the lethal consequences of acute chemical-induced lung damage. |
format | Online Article Text |
id | pubmed-7131465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1986 |
publisher | Published by Elsevier Ireland Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71314652020-04-08 A germ-free status does not protect from the lethal effects of acute lung damage caused by o,s,s,-trimethyl phosphorodithioate Nemery, B. Tucker, D.K. Sparrow, S. Toxicol Lett Article To investigate whether a normal resident microbiological flora of conventional rats influences the lethality of chemical-induced lung damage, the pneumotoxin O,S,S-trimethyl phosphorodithioate (OSSMe, 75 or 100 mg/kg, s.c.) was administered to age-matched conventional and germ-free male F344 rats. Microbiological and serological examinations confirmed the germ-free state of the germ-free rats and showed that no specific lung pathogens were present in the conventional rats. As in conventional rats, clinical symptoms and death of OSSMe-treated germ-free rats resulted from respiratory failure. The germ-free rats were not more resistant, but rather more susceptible to OSSMe than conventional rats. Increases in lung weight and histological examination of lung tissue 3 days after dosing with OSSMe (75 mg/kg, s.c.) showed no differences between germ-free and conventional rats. Despite alterations in their nasopharyngeal flora, death in the conventional rats was probably not caused by bacterial superinfection. The higher susceptibility of germ-free rats to OSSMe can be partly attributed to pharmacokinetic differences, since plasma levels of OSSMe decreased more slowly in germ-free than in conventional rats. It is concluded that germ-free rats are not protected from the lethal consequences of acute chemical-induced lung damage. Published by Elsevier Ireland Ltd. 1986 2002-11-21 /pmc/articles/PMC7131465/ /pubmed/3738927 http://dx.doi.org/10.1016/0378-4274(86)90062-7 Text en Copyright © 1986 Published by Elsevier Ireland Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Nemery, B. Tucker, D.K. Sparrow, S. A germ-free status does not protect from the lethal effects of acute lung damage caused by o,s,s,-trimethyl phosphorodithioate |
title | A germ-free status does not protect from the lethal effects of acute lung damage caused by o,s,s,-trimethyl phosphorodithioate |
title_full | A germ-free status does not protect from the lethal effects of acute lung damage caused by o,s,s,-trimethyl phosphorodithioate |
title_fullStr | A germ-free status does not protect from the lethal effects of acute lung damage caused by o,s,s,-trimethyl phosphorodithioate |
title_full_unstemmed | A germ-free status does not protect from the lethal effects of acute lung damage caused by o,s,s,-trimethyl phosphorodithioate |
title_short | A germ-free status does not protect from the lethal effects of acute lung damage caused by o,s,s,-trimethyl phosphorodithioate |
title_sort | germ-free status does not protect from the lethal effects of acute lung damage caused by o,s,s,-trimethyl phosphorodithioate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131465/ https://www.ncbi.nlm.nih.gov/pubmed/3738927 http://dx.doi.org/10.1016/0378-4274(86)90062-7 |
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