Modulation of Lung Allergic Response by Renal Ischemia and Reperfusion Injury


Autoria(s): Campanholle, Gabriela; Silva, Reinaldo C.; Martins, Joilson de Oliveira; Landgraf, Maristella A.; Paiva, Vanessa N.; Ferreira, Renaide R.; Amano, Mariane T.; Hiyane, Meire I.; Cenedeze, Marcos A.; Pacheco-Silva, Alvaro; Câmara, Niels Olsen Saraiva; Landgraf, Richardt G.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

06/11/2013

06/11/2013

2012

Resumo

The Th1/Th2 balance represents an important factor in the pathogenesis of renal ischemia-reperfusion injury (IRI). In addition, IRI causes a systemic inflammation that can affect other tissues, such as the lungs. To investigate the ability of renal IRI to modulate pulmonary function in a specific model of allergic inflammation, C57Bl/6 mice were immunized with ovalbumin/albumen on days 0 and 7 and challenged with an ovalbumin (OA) aerosol on days 14 and 21. After 24 h of the second antigen challenge, the animals were subjected to 45 minutes of ischemia. After 24 h of reperfusion, the bronchoalveolar lavage (BAL) fluid, blood and lung tissue were collected for analysis. Serum creatinine levels increased in both allergic and non-immunized animals subjected to IRI. However, BAL analysis showed a reduction in the total cells (46%) and neutrophils (58%) compared with control allergic animals not submitted to IRI. In addition, OA challenge induced the phosphorylation of ERK and Akt and the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) in lung homogenates. After renal IRI, the phosphorylation of ERK and expression of COX-2 and iNOS were markedly reduced; however, there was no difference in the phosphorylation of Akt between sham and ischemic OA-challenged animals. Mucus production was also reduced in allergic mice after renal IRI. IL-4, IL-5 and IL-13 were markedly down-regulated in immunized/challenged mice subjected to IRI. These results suggest that renal IRI can modulate lung allergic inflammation, probably by altering the Th1/Th2 balance and, at least in part, by changing cellular signal transduction factors. Copyright (C) 2012 S. Karger AG, Basel

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Fundacao de Auxilio aos Docentes e Alunos-UNIFESP (FADA)

Fundacao de Auxilio aos Docentes e AlunosUNIFESP (FADA)

Complex Fluids INCT

Complex Fluids INCT

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [07/07139-3, 10/01404-0]

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

Identificador

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, BASEL, v. 29, n. 41367, p. 523-532, SEP 28, 2012

1015-8987

http://www.producao.usp.br/handle/BDPI/42264

10.1159/000338506

http://dx.doi.org/10.1159/000338506

Idioma(s)

eng

Publicador

KARGER

BASEL

Relação

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Direitos

openAccess

Copyright KARGER

Palavras-Chave #ASTHMA #RENAL ISCHEMIA AND REPERFUSION #TH1/TH2 BALANCE #LUNG ALLERGIC INFLAMMATION #IRI #NITRIC-OXIDE SYNTHASE #SCHISTOSOMA-MANSONI INFECTION #ISCHEMIA/REPERFUSION INJURY #EOSINOPHIL INFILTRATION #MOUSE STRAINS #MURINE ASTHMA #MODEL #FAILURE #AIRWAY #KINASE #CELL BIOLOGY #PHYSIOLOGY
Tipo

article

original article

publishedVersion