Abstract

BackgroundPostoperative acute lung injury (ALI) is a severe complication after liver transplantation, which influences patient survival rate obviously. However, its mechanisms are unclear and effective therapies are still lacking. The current study focused on effects of propofol on liver transplantation-induced ALI and whether its underlying mechanism was relative with connexin43 (Cx43) alternation. The authors postulated that endotoxin induced enhancement of Cx43 gap junction (GJ) plays a critical role in mediating post liver transplantation ALI and that pretreatment with the anesthetic propofol, known to inhibit gap junction, can confer effective protection.MethodsMale Sprague–Dawley rats underwent autologous orthotopic liver transplantation (AOLT) in the absence or presence of treatments with the selective Cx43 inhibitor, enanthol (0.1 mg/kg) and propofol (50 mg/kg), a commonly used anesthetic in clinical anesthesia. In vitro study, BEAS-2B cells, a kind of lung epithelial cell line expressing Cx43, exposed to lipopolysaccharide (LPS), which mainly contributed to ALI. Function of Cx43 GJ was regulated by Cx43 specific inhibitors, gap26 (300 μM) or enhancer, retinoic acid (10 μM) and two specific siRNAs.ResultsCompared with the sham group, AOLT results in ALI obviously with plasma endotoxin increase. Cx43 inhibition decreased ALI through inflammatory reaction reduction. In vitro studies, LPS-induced BEAS-2B cells damage was attenuated by Cx43 function inhibition, but amplified by enhancement. Another important finding was propofol reduced Cx43 function and protected against LPS-mediated BEAS-2B cells damage or AOLT-induced ALI, mechanisms of which were also associated with inflammatory reaction decrease.ConclusionCx43 plays a vital role in liver transplantation-induced ALI. Propofol decreased Cx43 function and protected against ALI in vivo and in vitro. This finding provide a new basis for targeted intervention of organ protection in liver transplantation, even in other kinds of operations.

Highlights

  • Postoperative acute lung injury (ALI) is a severe complication after liver transplantation, which influences patient survival rate obviously

  • ALI contributed to mortality of patients suffering from liver transplantation, because patients with ALI prone to develop acute respiratory distress syndrome (ARDS), mortality rate among of which could be as high as 76.5 % [6, 7]

  • Inhibition gap junction (GJ) composed of Cx43 alleviated ALI followed autologous orthotopic liver transplantation (AOLT) Rat AOLT model was established to explore effects of liver transplantation on lungs

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Summary

Introduction

Postoperative acute lung injury (ALI) is a severe complication after liver transplantation, which influences patient survival rate obviously. The current study focused on effects of propofol on liver transplantation-induced ALI and whether its underlying mechanism was relative with connexin (Cx43) alternation. ALI contributed to mortality of patients suffering from liver transplantation, because patients with ALI prone to develop acute respiratory distress syndrome (ARDS), mortality rate among of which could be as high as 76.5 % [6, 7]. Mechanisms of this complication are still unclear and effective therapies are lacking. That is one of the key point in our investigation

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