Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Nemery, B., Tucker, D.K., Sparrow, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ireland Ltd. 1986
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
_version_ 1783517245455990784
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
work_keys_str_mv AT nemeryb agermfreestatusdoesnotprotectfromthelethaleffectsofacutelungdamagecausedbyosstrimethylphosphorodithioate
AT tuckerdk agermfreestatusdoesnotprotectfromthelethaleffectsofacutelungdamagecausedbyosstrimethylphosphorodithioate
AT sparrows agermfreestatusdoesnotprotectfromthelethaleffectsofacutelungdamagecausedbyosstrimethylphosphorodithioate
AT nemeryb germfreestatusdoesnotprotectfromthelethaleffectsofacutelungdamagecausedbyosstrimethylphosphorodithioate
AT tuckerdk germfreestatusdoesnotprotectfromthelethaleffectsofacutelungdamagecausedbyosstrimethylphosphorodithioate
AT sparrows germfreestatusdoesnotprotectfromthelethaleffectsofacutelungdamagecausedbyosstrimethylphosphorodithioate