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Critical Care 2011
Injurious mechanical ventilation affects neuronal activation in ventilated ratsDOI: 10.1186/cc10230 Abstract: Male Sprague Dawley rats were randomized to three groups: 1) Basal: anesthetized unventilated animals, 2) low Vt (LVt): MV for three hours with Vt 8 ml/kg and zero positive end-expiratory pressure (ZEEP), and 3) high Vt (HVt) MV for three hours with Vt 30 ml/kg and ZEEP. We measured lung mechanics, mean arterial pressure (MAP), arterial blood gases, and plasma and lung levels of cytokines. We used immunohistochemistry to examine c-fos as a marker of neuronal activation. An additional group of spontaneously breathing rats was added to discriminate the effect of surgical procedure and anesthesia in the brain.After three hours on LVt, PaO2 decreased and PaCO2 increased significantly. MAP and compliance remained stable in MV groups. Systemic and pulmonary inflammation was higher in MV rats than in unventilated rats. Plasma TNFα was significantly higher in HVt than in LVt. Immunopositive cells to c-fos in the retrosplenial cortex and thalamus increased significantly in HVt rats but not in LVt or unventilated rats.MV promoted brain activation. The intensity of the response was higher in HVt animals, suggesting an iatrogenic effect of MV on the brain. These findings suggest that this novel cross-talking mechanism between the lung and the brain should be explored in patients undergoing MV.Acute lung injury (ALI) and the acute respiratory distress syndrome (ARDS) are associated with high morbidity and mortality [1], and ARDS survivors present significant long-term cognitive impairment [2]. These consequences may result from complex interactions between different clinical protocols and endogenous factors occurring simultaneously in critically ill patients [3]. In this context, mechanical ventilation (MV) is a lifesaving procedure but not without complications. Even in healthy lungs, MV may contribute to a positive feedback loop that starts with mechanotransduction (in lungs) at the epithelial and endothelial levels leading to a deleterious inflammatory cascade that might affe
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