Pulmonary Capillary Endothelium-Bound Angiotensin-Converting Enzyme Activity in Acute Lung Injury

Author:

Orfanos Stylianos E.1,Armaganidis Apostolos1,Glynos Constantinos1,Psevdi Ekaterini1,Kaltsas Panagiotis1,Sarafidou Paulina1,Catravas John D.1,Dafni Urania G.1,Langleben David1,Roussos Charis1

Affiliation:

1. From the Critical Care Department, Evangelismos Hospital, University of Athens Medical School (S.E.O., A.A., C.G., E.P., P.K., P.S., C.R.), and Department of Nursing, University of Athens (U.G.D.), Greece; the Vascular Biology Center, Medical College of Georgia, Augusta (J.D.C.); and the Division of Cardiology, Jewish General Hospital, McGill University, Montreal, Quebec, Canada (D.L.).

Abstract

Background—Pulmonary capillary endothelium-bound (PCEB) angiotensin-converting ectoenzyme (ACE) activity alteration is an early, sensitive, and quantifiable lung injury index in animal models. We hypothesized that (1) PCEB-ACE alterations can be found in patients with acute lung injury (ALI) and (2) PCEB-ACE activity correlates with the severity of lung injury and may be used as a quantifiable marker of the underlying pulmonary capillary endothelial dysfunction.Methods and Results—Applying indicator-dilution techniques, we measured single-pass transpulmonary hydrolysis of the synthetic ACE substrate3H-benzoyl-Phe-Ala-Pro (BPAP) in 33 mechanically ventilated, critically ill patients with a lung injury score (LIS) ranging from 0 (no lung injury) to 3.7 (severe lung injury) and calculated the kinetic parameter Amax/Km. Both parameters decreased early during the ALI continuum and were inversely related to APACHE II score and LIS. Hydrolysis decreased with increasing cardiac output (CO), whereas 2 different patterns were observed between CO and Amax/Km.Conclusions—PCEB-ACE activity decreases early during ALI, correlates with the clinical severity of both the lung injury and the underlying disease, and may be used as a quantifiable marker of underlying pulmonary capillary endothelial dysfunction.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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