Abstract

BackgroundPulmonary edema is a hallmark of acute respiratory distress syndrome (ARDS). Smoke inhalation causes ARDS, thus significantly increasing the mortality of burn patients. Adipose-derived stem cells (ASCs) exert potent anti-inflammatory properties. The goal of the present study was to test the safety and ecfficacy of ASCs, in a well-characterized clinically relevant ovine model of ARDS.MethodsFemale sheep were surgically prepared. ARDS was induced by cooled cotton smoke inhalation. Following injury, sheep were ventilated, resuscitated with lactated Ringer’s solution, and cardiopulmonary hemodynamics were monitored for 48 hours in a conscious state. Pulmonary microvascular hyper-permeability was assessed by measuring lung lymph flow, extravascular lung water content, protein content in plasma and lung lymph fluid. Sheep were randomly allocated to two groups: 1) ASCs: infused with 200 million of ASCs in 200mL of PlasmaLyteA starting 1 hours post-injury, n = 5; 2) control, treated with 200mL of PlasmaLyteA in a similar pattern, n = 5.ResultsLung lymph flow increased 9-fold in control sheep as compared to baseline. Protein in the plasma was significantly decreased, while it was increased in the lung lymph. The treatment with ASCs significantly attenuated these changes. Treatment with ASCs almost led to the reversal of increased pulmonary vascular permeability and lung water content. Pulmonary gas exchange was significantly improved by ASCs. Infusion of the ASCs did not negatively affect pulmonary artery pressure and other hemodynamic variables.ConclusionsASCs infusion was well tolerated. The results suggest that intravenous ASCs modulate pulmonary microvascular hyper-permeability and prevent the onset of ARDS in our experimental model.

Highlights

  • Treatment with Adipose-derived stem cells (ASCs) almost led to the reversal of increased pulmonary vascular permeability and lung water content

  • Pulmonary gas exchange was significantly improved by ASCs

  • The results suggest that intravenous ASCs modulate pulmonary microvascular hyper-permeability and prevent the onset of Acute respiratory distress syndrome (ARDS) in our experimental model

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Summary

Introduction

Acute respiratory distress syndrome (ARDS) is a severe form of acute lung injury caused by sepsis, pneumonia, trauma, severe burn, and smoke inhalation injury [1]. Pathophysiological changes in the lungs after smoke inhalation injury are characterized by increased pulmonary microvascular permeability, edema formation, and airway obstruction. Neurogenic inflammation results in narrowing of airway lumina, which is attributable to airway mucosal hyperaemia, formation of obstructive casts in the airway, and bronchospasm. These changes result in severe impairment of respiratory gas exchange [3]. Smoke inhalation causes ARDS, significantly increasing the mortality of burn patients. The goal of the present study was to test the safety and ecfficacy of ASCs, in a well-characterized clinically relevant ovine model of ARDS

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