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Neutrophil endopeptidase inhibitor improves pulmonary function during reperfusion after eighteen-hour preservation
- Source :
- The Journal of thoracic and cardiovascular surgery. 112(3)
- Publication Year :
- 1996
-
Abstract
- Background: Reperfusion injury remains a significant problem after lung transplantation and is thought to be in part mediated by neutrophils. Ulinastatin inhibits release of elastase and cathepsin G from neutrophil granules. We hypothesized that inhibition of these neutrophil endopeptidases (proteases) would attenuate pulmonary reperfusion injury. Methods: With an isolated, whole blood–perfused, ventilated rabbit lung model, we studied the effects of ulinastatin. All lungs were flushed with cold Euro-Collins solution, harvested en bloc, stored inflated at 4° C for 18 hours, and reperfused with whole blood. The 18-hour control lungs ( n = 8) were stored and reperfused. Low-dose ( n = 8) and high-dose ( n = 7) groups were treated with total doses of ulinastatin of 25,000 and 50,000 units, respectively, during flush and reperfusion. An additional control group of lungs ( n = 8) was harvested, flushed, and immediately reperfused. Results: The pulmonary artery pressure was significantly lower in the high-dose group than in the 18-hour control group (36.7 ± 1.8 vs 44.8 ± 2.9 mm Hg, p = 0.034). The percentage decrease in dynamic airway compliance was significantly less in the high-dose group than in the 18-hour control group (-13.8% ± 4.4% vs -25.1% ± 3.7%, p = 0.032). Both low-dose and high-dose ulinastatin treatments did not result in a significant improvement in oxygenation with respect to the 18-hour control group (72.2 ± 25.8 vs 32.5 ± 4.9 mm Hg, p = 0.21). Conclusions: Ulinastatin diminishes reperfusion injury after 18 hours of hypothermic pulmonary ischemia, with resultant improvements in pulmonary artery pressure and airway compliance. Improvement in pulmonary function after preservation and reperfusion with a neutrophil endopeptidase inhibitor confirms the role of endopeptidases in reperfusion injury and suggests an intervention to reduce their detrimental effects on early graft function. (J THORAC CARDIOVASC SURG 1996;112:607-13)
- Subjects :
- Male
Cathepsin G
Neutrophils
medicine.medical_treatment
Hypertonic Solutions
Blood Pressure
030204 cardiovascular system & hematology
Pulmonary function testing
chemistry.chemical_compound
0302 clinical medicine
Hypothermia, Induced
Lung Compliance
Pancreatic Elastase
Elastase
Serine Endopeptidases
Organ Preservation
3. Good health
medicine.anatomical_structure
030220 oncology & carcinogenesis
Anesthesia
Reperfusion Injury
Female
Rabbits
Cardiology and Cardiovascular Medicine
Trypsin Inhibitors
Lung Transplantation
Pulmonary and Respiratory Medicine
Serine Proteinase Inhibitors
Pulmonary Artery
03 medical and health sciences
Oxygen Consumption
medicine.artery
medicine
Lung transplantation
Animals
Protease Inhibitors
Glycoproteins
Lung
business.industry
medicine.disease
Ulinastatin
Cathepsins
chemistry
Pulmonary artery
Reperfusion
Surgery
business
Leukocyte Elastase
Reperfusion injury
Subjects
Details
- ISSN :
- 00225223
- Volume :
- 112
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- The Journal of thoracic and cardiovascular surgery
- Accession number :
- edsair.doi.dedup.....d04c55cd2f61010d05002635bd15c79c