Intestinal Lymph-Borne Factors Induce Lung Release of Inflammatory Mediators and Expression of Adhesion Molecules After an Intestinal Ischemic Insult


Autoria(s): Faloppa, Ana Cristina Breithaupt; Vitoretti, Luana Beatriz; Cavriani, Gabriela; Franco, Adriana Lino dos Santos; Hayashi, Lia Siguemi Sudo; Filho, Ricardo Martins de Oliveira; Vargaftig, Bernardo Boris Jorge; Lima, Wothan Tavares de
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

06/11/2013

06/11/2013

2012

Resumo

Background. Intestinal ischemia and reperfusion (I/R) is a documented cause of acute lung injury (ALI) and systemic inflammation. We previously reported that obstruction of thoracic lymphatic flow during intestinal I/R blunts pulmonary neutrophil recruitment and microvascular injury and decreases the systemic levels of tumor necrosis factor. Here, we consider the existence of a gut-lung axis promoting the induction of systemic inflammation, whereby drained intestinal lymph stimulates lung expression of adhesion molecules and matrix components and generation of inflammatory mediators. Material and Methods. Upon administration of anesthesia, male Wistar rats were subjected to occlusion of the superior mesenteric artery for 45 min, followed by 2 h of intestinal reperfusion (I/R); groups of rats were subjected to I/R with or without thoracic lymphatic duct ligation immediately before the procedure. The non-manipulated rats were used to investigate basal parameters. Results. Obstruction of thoracic lymphatic flow before intestinal I/R decreased the ability of cultured lung tissue explants to release IL-1 beta, IL-10, and VEGF. In contrast, lymphatic obstruction normalized the elevated lung expression of PECAM-1 caused by intestinal I/R. On the other hand, lung E-selectin expression was significantly reduced, whereas fibronectin expression and collagen synthesis were not affected. Lymph levels of LTB4 and TXB2 were found to be significantly increased. Conclusions. These data suggest that lymph factors drained from the intestine during ischemic trauma stimulate the lung to generate inflammatory mediators and alter the expression of adhesion molecules. Disturbances in lung homeostasis mediated by lymph might contribute to the spread of inflammatory processes, thereby accounting for the systemic inflammation induced by intestinal I/R. (C) 2012 Elsevier Inc. All rights reserved.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [FAPESP: 02/06606, 05/02271-5, 2007/07139-3, 2009/54823-2]

Conselho Nacional de Pesquisa (CNPq)

Conselho Nacional de Pesquisa (CNPq)

Identificador

JOURNAL OF SURGICAL RESEARCH, SAN DIEGO, v. 176, n. 1, supl. 4, Part 1-2, pp. 195-201, JUL, 2012

0022-4804

http://www.producao.usp.br/handle/BDPI/42584

10.1016/j.jss.2011.06.074

http://dx.doi.org/10.1016/j.jss.2011.06.074

Idioma(s)

eng

Publicador

ACADEMIC PRESS INC ELSEVIER SCIENCE

SAN DIEGO

Relação

JOURNAL OF SURGICAL RESEARCH

Direitos

closedAccess

Copyright ACADEMIC PRESS INC ELSEVIER SCIENCE

Palavras-Chave #INTESTINAL ISCHEMIA/REPERFUSION #LYMPHATIC SYSTEM #LUNG INFLAMMATION #INFLAMMATORY MEDIATORS #ADHESION MOLECULES #RAT #RESPIRATORY-DISTRESS-SYNDROME #NECROSIS-FACTOR-ALPHA #HEMORRHAGIC-SHOCK #MESENTERIC LYMPH #DUCT LIGATION #NITRIC-OXIDE #LEUKOCYTE ADHESION #THROMBOXANE A(2) #THORACIC-DUCT #INJURY #SURGERY
Tipo

article

original article

publishedVersion