Connective tissue mast cells are the target of formaldehyde to induce tracheal hyperresponsiveness in rats: Putative role of leukotriene B(4) and nitric oxide


Autoria(s): LINO-DOS-SANTOS-FRANCO, Adriana; SHIA, Mey Kuang; DOMINGOS, Helori Vanni; BREITHAUPT-FALOPPA, Ana Cristina; OLIVEIRA, Ana Paula Ligeiro de; OLIVEIRA-FILHO, Ricardo Martins; VARGAFTIG, B. Boris; TAVARES-DE-LIMA, Wothan
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Formaldehyde (FA) exposure induces upper airways irritation and respiratory abnormalities, but its mechanisms are not understood. Since mast cells are widely distributed in the airways, we hypothesized that FA might modify the airways reactivity by mechanism involving their activation. Tracheal rings of rats were incubated with Dulbecco`s modified medium culture containing FA (0.1 ppm) in 96-well plastic microplates in a humid atmosphere. After 30 min, 6 h, and 24-72 h, the rings were suspended in an organ bath and dose-response curve to methacholine (MCh) were determined. incubation with FA caused a transient tracheal hyperresponsiveness to MCh that was independent from tracheal epithelium integrity. Connective tissue mast cell depletion caused by compound 48/80 or mast cell activation by the allergic reaction, before exposure of tracheal rings to FA prevented the increased responsiveness to MCh. LTB(4) concentrations were increased in the culture medium of tracheas incubated with FA for 48 h, whereas the LTB(4)-receptor antagonist MK886 (1 mu M) added before FA exposure rendered the tracheal rings normoreactive to MCh. In addition, FA exposure did not cause hyperresponsiveness in tracheal segments incubated with L-arginine (1 mu M). We suggest that airway connective tissue mast cells constitute the target and may provide the increased LTB(4) generation as well as an elevated consumption of NO leading to tracheal hyperresponsiveness to MCh. (C) 2009 Elsevier Ireland Ltd. All rights reserved.

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundacao de Amparo Pesquisa do Estado de Sao Paulo (FAPESP)[02/06606-3]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundacao de Amparo Pesquisa do Estado de Sao Paulo (FAPESP)[01/11417-2]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundacao de Amparo Pesquisa do Estado de Sao Paulo (FAPESP)[08/50766-1]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Conselho Nacional de Pesquisa (CNPq)

Identificador

TOXICOLOGY LETTERS, v.192, n.2, p.85-90, 2010

0378-4274

http://producao.usp.br/handle/BDPI/28700

10.1016/j.toxlet.2009.10.006

http://dx.doi.org/10.1016/j.toxlet.2009.10.006

Idioma(s)

eng

Publicador

ELSEVIER IRELAND LTD

Relação

Toxicology Letters

Direitos

restrictedAccess

Copyright ELSEVIER IRELAND LTD

Palavras-Chave #Formaldehyde #Connective tissue mast cells #Methacholine #Leukotriene B(4) #Nitric oxide #Airway responsiveness #Rat #S-NITROSOGLUTATHIONE REDUCTASE #COMPOUND 48/80 #SMOOTH-MUSCLE #INFLAMMATION #MEDIATORS #RESPONSES #RELEASE #ASTHMA #BRONCHOCONSTRICTION #STIMULATION #Toxicology
Tipo

article

original article

publishedVersion