Cargando…

Inhalation exposure to nanosized and fine TiO(2 )particles inhibits features of allergic asthma in a murine model

BACKGROUND: Nanotechnology and engineered nanomaterials (ENM) are here to stay. Recent evidence suggests that exposure to environmental particulate matter exacerbates symptoms of asthma. In the present study we investigated the modulatory effects of titanium dioxide particle exposure in an experimen...

Descripción completa

Detalles Bibliográficos
Autores principales: Rossi, Elina M, Pylkkänen, Lea, Koivisto, Antti J, Nykäsenoja, Heli, Wolff, Henrik, Savolainen, Kai, Alenius, Harri
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3003234/
https://www.ncbi.nlm.nih.gov/pubmed/21108815
http://dx.doi.org/10.1186/1743-8977-7-35
_version_ 1782193842852724736
author Rossi, Elina M
Pylkkänen, Lea
Koivisto, Antti J
Nykäsenoja, Heli
Wolff, Henrik
Savolainen, Kai
Alenius, Harri
author_facet Rossi, Elina M
Pylkkänen, Lea
Koivisto, Antti J
Nykäsenoja, Heli
Wolff, Henrik
Savolainen, Kai
Alenius, Harri
author_sort Rossi, Elina M
collection PubMed
description BACKGROUND: Nanotechnology and engineered nanomaterials (ENM) are here to stay. Recent evidence suggests that exposure to environmental particulate matter exacerbates symptoms of asthma. In the present study we investigated the modulatory effects of titanium dioxide particle exposure in an experimental allergic asthma. METHODS: Nonallergic (healthy) and ovalbumin-sensitized (asthmatic) mice were exposed via inhalation to two different sizes of titanium dioxide particles, nanosized (nTiO(2)) and fine (fTiO(2)), for 2 hours a day, three days a week, for four weeks at a concentration of 10 mg/m(3). Different endpoints were analysed to evaluate the immunological status of the mice. RESULTS: Healthy mice elicited pulmonary neutrophilia accompanied by significantly increased chemokine CXCL5 expression when exposed to nTiO(2). Surprisingly, allergic pulmonary inflammation was dramatically suppressed in asthmatic mice which were exposed to nTiO(2 )or fTiO(2 )particles - i.e. the levels of leucocytes, cytokines, chemokines and antibodies characteristic to allergic asthma were substantially decreased. CONCLUSIONS: Our results suggest that repeated airway exposure to TiO(2 )particles modulates the airway inflammation depending on the immunological status of the exposed mice.
format Text
id pubmed-3003234
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-30032342010-12-18 Inhalation exposure to nanosized and fine TiO(2 )particles inhibits features of allergic asthma in a murine model Rossi, Elina M Pylkkänen, Lea Koivisto, Antti J Nykäsenoja, Heli Wolff, Henrik Savolainen, Kai Alenius, Harri Part Fibre Toxicol Research BACKGROUND: Nanotechnology and engineered nanomaterials (ENM) are here to stay. Recent evidence suggests that exposure to environmental particulate matter exacerbates symptoms of asthma. In the present study we investigated the modulatory effects of titanium dioxide particle exposure in an experimental allergic asthma. METHODS: Nonallergic (healthy) and ovalbumin-sensitized (asthmatic) mice were exposed via inhalation to two different sizes of titanium dioxide particles, nanosized (nTiO(2)) and fine (fTiO(2)), for 2 hours a day, three days a week, for four weeks at a concentration of 10 mg/m(3). Different endpoints were analysed to evaluate the immunological status of the mice. RESULTS: Healthy mice elicited pulmonary neutrophilia accompanied by significantly increased chemokine CXCL5 expression when exposed to nTiO(2). Surprisingly, allergic pulmonary inflammation was dramatically suppressed in asthmatic mice which were exposed to nTiO(2 )or fTiO(2 )particles - i.e. the levels of leucocytes, cytokines, chemokines and antibodies characteristic to allergic asthma were substantially decreased. CONCLUSIONS: Our results suggest that repeated airway exposure to TiO(2 )particles modulates the airway inflammation depending on the immunological status of the exposed mice. BioMed Central 2010-11-25 /pmc/articles/PMC3003234/ /pubmed/21108815 http://dx.doi.org/10.1186/1743-8977-7-35 Text en Copyright ©2010 Rossi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Rossi, Elina M
Pylkkänen, Lea
Koivisto, Antti J
Nykäsenoja, Heli
Wolff, Henrik
Savolainen, Kai
Alenius, Harri
Inhalation exposure to nanosized and fine TiO(2 )particles inhibits features of allergic asthma in a murine model
title Inhalation exposure to nanosized and fine TiO(2 )particles inhibits features of allergic asthma in a murine model
title_full Inhalation exposure to nanosized and fine TiO(2 )particles inhibits features of allergic asthma in a murine model
title_fullStr Inhalation exposure to nanosized and fine TiO(2 )particles inhibits features of allergic asthma in a murine model
title_full_unstemmed Inhalation exposure to nanosized and fine TiO(2 )particles inhibits features of allergic asthma in a murine model
title_short Inhalation exposure to nanosized and fine TiO(2 )particles inhibits features of allergic asthma in a murine model
title_sort inhalation exposure to nanosized and fine tio(2 )particles inhibits features of allergic asthma in a murine model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3003234/
https://www.ncbi.nlm.nih.gov/pubmed/21108815
http://dx.doi.org/10.1186/1743-8977-7-35
work_keys_str_mv AT rossielinam inhalationexposuretonanosizedandfinetio2particlesinhibitsfeaturesofallergicasthmainamurinemodel
AT pylkkanenlea inhalationexposuretonanosizedandfinetio2particlesinhibitsfeaturesofallergicasthmainamurinemodel
AT koivistoanttij inhalationexposuretonanosizedandfinetio2particlesinhibitsfeaturesofallergicasthmainamurinemodel
AT nykasenojaheli inhalationexposuretonanosizedandfinetio2particlesinhibitsfeaturesofallergicasthmainamurinemodel
AT wolffhenrik inhalationexposuretonanosizedandfinetio2particlesinhibitsfeaturesofallergicasthmainamurinemodel
AT savolainenkai inhalationexposuretonanosizedandfinetio2particlesinhibitsfeaturesofallergicasthmainamurinemodel
AT aleniusharri inhalationexposuretonanosizedandfinetio2particlesinhibitsfeaturesofallergicasthmainamurinemodel