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Pulmonary Effects of Adjusting Tidal Volume to Actual or Ideal Body Weight in Ventilated Obese Mice

Obese patients could be more susceptible to mechanical ventilation (MV)-induced lung injury than non-obese patients due to weight-dependent changes in lung properties. The aim of this study was therefore to evaluate the pulmonary effects of 2 hours low V(T) MV in a diet-induced obese mice model, wit...

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Detalles Bibliográficos
Autores principales: Guivarch, Elise, Voiriot, Guillaume, Rouzé, Anahita, Kerbrat, Stéphane, Tran Van Nhieu, Jeanne, Montravers, Philippe, Maitre, Bernard, Mekontso Dessap, Armand, Desmard, Mathieu, Boczkowski, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915403/
https://www.ncbi.nlm.nih.gov/pubmed/29691422
http://dx.doi.org/10.1038/s41598-018-24615-5
Descripción
Sumario:Obese patients could be more susceptible to mechanical ventilation (MV)-induced lung injury than non-obese patients due to weight-dependent changes in lung properties. The aim of this study was therefore to evaluate the pulmonary effects of 2 hours low V(T) MV in a diet-induced obese mice model, with V(T) calculated on either the actual body weight (V(T)aw) or the ideal body weight (V(T)iw) . First, we hypothesized that a MV with V(T)aw would be associated with altered lung mechanics and an increased lung inflammation. Second, we hypothesised that a MV with a V(T)iw would preserve lung mechanics and limit lung inflammation. We analyzed lung mechanics and inflammation using bronchoalveolar lavage (BAL) cell counts, flow cytometry tissue analysis and histology. Lung mechanics and inflammation were comparable in control and obese mice receiving V(T)iw. By contrast, obese mice receiving V(T)aw had significantly more alterations in lung mechanics, BAL cellularity and lung influx of monocytes as compared to control mice. Their monocyte expression of Gr1 and CD62L was also increased. Alveolar neutrophil infiltration was significantly increased in all obese mice as compared to controls. In conclusion, our findings suggest that protective MV with a V(T)aw is deleterious, with a marked alteration in lung mechanics and associated lung inflammation as compared to lean mice. With V(T)iw, lung mechanics and inflammation were close to that of control mice, except for an increased alveolar infiltrate of polymorphonuclear neutrophils. This inflammation might be attenuated by a blunted recruitment of inflammatory cells associated with obesity.