Prolonged hypercapnia is commonly encountered during the treatment of acute respiratory distress syndrome and acute respiratory failure attributable to other causes with protective ventilation strategies. In these circumstances, compensatory renal buffering returns pH to normal establishing a condition of buffered hypercapnia. It is also common intensive care practice to correct the pH more rapidly using bicarbonate infusions. Although it is well-established that hypercapnic acidosis has potent anti-inflammatory and protective effects, the effect of buffered hypercapnia on acute lung injury and acute respiratory distress syndrome is unknown. We therefore wished to determine the effects of buffered hypercapnia on acute lung injury induced by endotoxin or Escherichia coli infection in vivo.
Prospective, randomized animal study.
University research laboratory.
Adult male Sprague-Dawley rats.
We established buffered hypercapnia by exposing rats to a hypercapnic environment for 3 days before the induction of lung injury. Buffered hypercapnia rats (initial pH >7.35, FiCO2 = 0.05) and normocapnic controls (initial pH >7.35, FiCO2 = 0.00) were then anesthetized, mechanically ventilated, and lung injury induced by intra-tracheal inoculation of endotoxin (series I) or Escherichia coli (series II).
Buffered hypercapnia significantly increased both endotoxin and Escherichia coli-induced lung injury when compared to normocapnic controls, as assessed by arterial oxygenation, lung compliance, pro-inflammatory pulmonary cytokine concentrations, and measurements of structural lung damage. In additional in vitro experiments buffered hypercapnia did not alter neutrophil phagocytosis ability but did impaired epithelial wound healing.
Our results demonstrate that infection-induced injury in vivo is worsened after renal buffering of hypercapnic acidosis independently of any changes in tidal volume. These findings have important implications for our understanding of the pathogenesis of infection-induced lung injury during the use protective ventilation strategies that permits buffered hypercapnia and during infective exacerbations of chronic lung diseases associated with sustained hypercapnia.
From the School of Medicine and Medical Sciences (ADN, DFO, KH, FN, CO, PM), Conway Institute, University, College Dublin, Ireland; Department of Anaesthesia (JB), St. Vincent's University Hospital, Dublin, Ireland; Department of Anaesthesia (DO, JGL), Clinical Sciences Institute, National University of Ireland, Galway, and University College Hospital, Galway, Ireland.
Supported, in part, by grants from the Program for Research in Third Level Institutions, the Intensive Care Society of Ireland, the College of Anaesthetists Ireland, through its Abbott scholarship. A. Nichol was supported by an Embark Scholarship from the Irish Research Council for Science, Engineering, and Technology.
The authors have not disclosed any potential conflicts of interest.
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