Literature DB >> 14633514

Enhancement of the endotoxin recognition pathway by ventilation with a large tidal volume in rabbits.

Kiyoshi Moriyama1, Akitoshi Ishizaka, Morio Nakamura, Hiroshi Kubo, Toru Kotani, Shinichi Yamamoto, Eileen N Ogawa, Osamu Kajikawa, Charles W Frevert, Yoshifumi Kotake, Hiroshi Morisaki, Hidefumi Koh, Sadatomo Tasaka, Thomas R Martin, Junzo Takeda.   

Abstract

Ventilation with a small tidal volume (V(t)) is associated with better clinical outcomes than with a large V(t), particularly in critical settings, including acute lung injury. To determine whether V(t) influences the lipopolysaccaharide (LPS) recognition pathway, we studied CD14 expression in rabbit lungs and the release of TNF-alpha by cultured alveolar macrophages after 240 min of ventilation with a large (20 ml/kg) vs. a small (5 ml/kg) V(t). We also applied small or large V(t) to lungs instilled with 50 microg/kg of LPS. The alveolar macrophages collected after large V(t) ventilation revealed a 20-fold increase in LPS-induced TNF-alpha release compared with those collected after small V(t) ventilation, whereas TNF-alpha was undetectable without LPS stimulation. In animals ventilated with a large V(t), the expression of CD14 mRNA in whole lung homogenates and the expression of CD14 protein on alveolar macrophages, assessed by immunohistochemistry, were both significantly increased in the absence of LPS stimulation. A large V(t) applied to LPS-instilled lungs increased the pulmonary albumin permeability and TNF-alpha release into the plasma. These results suggest that mechanical stress caused by a large V(t) sensitizes the lungs to endotoxin, a phenomenon that may occur partially via the upregulation of CD14.

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Year:  2003        PMID: 14633514     DOI: 10.1152/ajplung.00296.2003

Source DB:  PubMed          Journal:  Am J Physiol Lung Cell Mol Physiol        ISSN: 1040-0605            Impact factor:   5.464


  22 in total

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Authors:  Pierre Emmanuel Charles; Saber Davide Barbar
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Review 2.  Innate immunity in the lungs.

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3.  Effects of age on the synergistic interactions between lipopolysaccharide and mechanical ventilation in mice.

Authors:  Lincoln S Smith; Sina A Gharib; Charles W Frevert; Thomas R Martin
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4.  Role of the pulmonary epithelium and inflammatory signals in acute lung injury.

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5.  Mechanical ventilation modulates Toll-like receptor signaling pathway in a sepsis-induced lung injury model.

Authors:  Jesús Villar; Nuria Cabrera; Milena Casula; Carlos Flores; Francisco Valladares; Mercedes Muros; Lluis Blanch; Arthur S Slutsky; Robert M Kacmarek
Journal:  Intensive Care Med       Date:  2010-04-16       Impact factor: 17.440

6.  The NLRP3 inflammasome is required for the development of hypoxemia in LPS/mechanical ventilation acute lung injury.

Authors:  Heather D Jones; Timothy R Crother; Romer A Gonzalez-Villalobos; Madhulika Jupelli; Shuang Chen; Jargalsaikhan Dagvadorj; Moshe Arditi; Kenichi Shimada
Journal:  Am J Respir Cell Mol Biol       Date:  2014-02       Impact factor: 6.914

7.  Mechanical ventilation modulates TLR4 and IRAK-3 in a non-infectious, ventilator-induced lung injury model.

Authors:  Jesús Villar; Nuria E Cabrera; Milena Casula; Carlos Flores; Francisco Valladares; Lucio Díaz-Flores; Mercedes Muros; Arthur S Slutsky; Robert M Kacmarek
Journal:  Respir Res       Date:  2010-03-03

8.  Toll-like receptor 4 mediates neutrophil sequestration and lung injury induced by endotoxin and hyperinflation.

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Journal:  Crit Care Med       Date:  2010-01       Impact factor: 7.598

9.  Interactions between mechanical and biological processes in acute lung injury.

Authors:  Thomas R Martin
Journal:  Proc Am Thorac Soc       Date:  2008-04-15

10.  Reduction in alveolar macrophages attenuates acute ventilator induced lung injury in rats.

Authors:  Fabien G Eyal; Charles R Hamm; James C Parker
Journal:  Intensive Care Med       Date:  2007-04-28       Impact factor: 17.440

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