Endothelial dysfunction in the pulmonary artery induced by concentrated fine particulate matter exposure is associated with local but not systemic inflammation


Autoria(s): Davel, Ana Paula Couto; Lemos, Miriam; Pastro, Luciana Manfre; Pedro, Sibelli Silva Cosme; André, Paulo Afonso de; Duarte, Cristina Bichels Hebeda; Farsky, Sandra Helena Poliselli; Saldiva, Paulo Hilario Nascimento; Rossoni, Luciana Venturini
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

30/10/2013

30/10/2013

02/08/2013

Resumo

Clinical evidence has identified the pulmonary circulation as an important target of air pollution. It was previously demonstrated that in vitro exposure to fine particulate matter (aerodynamic diameter <= 2.5 mu m, PM2.5) induces endothelial dysfunction in isolated pulmonary arteries. We aimed to investigate the effects of in vivo exposure to urban concentrated PM2.5 on rat pulmonary artery reactivity and the mechanisms involved. For this, adult Wistar rats were exposed to 2 weeks of concentrated Sao Paulo city air PM2.5 at an accumulated daily dose of approximately 600 mu g/m(3). Pulmonary arteries isolated from PM2.5-exposed animals exhibited impaired endothelium-dependent relaxation to acetylcholine without significant changes in nitric oxide donor response compared to control rats. PM2.5 caused vascular oxidative stress and enhanced protein expression of Cu/Zn- and Mn-superoxide dismutase in the pulmonary artery. Protein expression of endothelial nitric oxide synthase (eNOS) was reduced, while tumor necrosis factor (TNF)-alpha was enhanced by PM2.5 inhalation in pulmonary artery. There was a significant positive correlation between eNOS expression and maximal relaxation response (E-max) to acetylcholine. A negative correlation was found between vascular TNF-alpha expression and E-max to acetylcholine. Plasma cytokine levels, blood cells count and coagulation parameters were similar between control and PM2.5-exposed rats. The present findings showed that in vivo daily exposure to concentrated urban PM2.5 could decrease endothelium-dependent relaxation and eNOS expression on pulmonary arteries associated with local high TNF-alpha level but not systemic pro-inflammatory factors. Taken together, the present results elucidate the mechanisms underlying the trigger of cardiopulmonary diseases induced by urban ambient levels of PM2.5. (C) 2012 Elsevier Ireland Ltd. All rights reserved.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [02/09804-0, 08/54212-0]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) (Brazil)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Brazil

Identificador

TOXICOLOGY, CLARE, v. 295, n. 41334, supl. 1, Part 3, pp. 39-46, MAY 16, 2012

0300-483X

http://www.producao.usp.br/handle/BDPI/36796

10.1016/j.tox.2012.02.004

http://dx.doi.org/10.1016/j.tox.2012.02.004

Idioma(s)

eng

Publicador

ELSEVIER IRELAND LTD

CLARE

Relação

TOXICOLOGY

Direitos

closedAccess

Copyright ELSEVIER IRELAND LTD

Palavras-Chave #PARTICULATE MATTER #PULMONARY ARTERY #INFLAMMATORY CYTOKINES #OXIDATIVE STRESS #NITRIC OXIDE #NITRIC-OXIDE SYNTHASE #DIESEL EXHAUST INHALATION #NECROSIS-FACTOR-ALPHA #AIR-POLLUTION #SAO-PAULO #OXIDATIVE STRESS #DEPENDENT RELAXATION #CORONARY-ARTERIES #VASCULAR-DISEASE #NAD(P)H OXIDASE #PHARMACOLOGY & PHARMACY #TOXICOLOGY
Tipo

article

original article

publishedVersion