Vaporized perfluorocarbon confers protection against acute lung injury by inhibiting MMP-9 expression without protective effects in other organs

J Int Med Res. 2012;40(1):115-25. doi: 10.1177/147323001204000112.

Abstract

Objective: Vaporized perfluorocarbon (PFC) is a treatment for lung injury; this study investigated its mode of action and potential protective effects on other organs, which are unclear.

Methods: Acute lung injury was induced by lung lavage with artificial seawater in 32 female New Zealand White rabbits. Animals received either conventional mechanical ventilation (CMV), positive end-expiratory pressure under CMV (PEEP), vaporized PFC ventilation, or positive end-expiratory pressure with vaporized PFC ventilation (PEEP+PFC). Histopathology of the lung, small intestine, liver and kidney were investigated. Matrix metalloproteinase (MMP)-9 mRNA levels in the lung were analysed.

Results: Pathological injury of the lung was significantly alleviated in the PEEP, PFC and PEEP+PFC groups compared with the CMV group. Tissue damage in the liver, kidney and small intestine was similar between all groups. MMP-9 mRNA levels in the PEEP, PFC and PEEP+PFC groups were significantly lower than those in the CMV group.

Conclusions: Vaporized PFC ventilation can significantly alleviate lung injury but has no significant protective effect on other organs. Alleviation of lung injury may be associated with MMP-9 inhibition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury / enzymology*
  • Acute Lung Injury / pathology
  • Acute Lung Injury / physiopathology
  • Acute Lung Injury / prevention & control*
  • Animals
  • Disease Models, Animal
  • Female
  • Fluorocarbons / pharmacology*
  • Gene Expression Regulation, Enzymologic
  • Matrix Metalloproteinase 9 / genetics
  • Matrix Metalloproteinase 9 / metabolism
  • Matrix Metalloproteinase Inhibitors*
  • Organ Specificity / drug effects*
  • Oxygen / metabolism
  • Positive-Pressure Respiration
  • Protective Agents / pharmacology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rabbits
  • Respiration, Artificial
  • Volatilization / drug effects

Substances

  • Fluorocarbons
  • Matrix Metalloproteinase Inhibitors
  • Protective Agents
  • RNA, Messenger
  • Matrix Metalloproteinase 9
  • Oxygen