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Originally Published 30 March 1999
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Pulmonary Capillary Endothelium-Bound Angiotensin-Converting Enzyme Activity in Humans

Stylianos E. Orfanos, David Langleben, Joseph Khoury, Robert D. Schlesinger, Leonidas Dragatakis, Charis Roussos, James W. Ryan, and John D. CatravasAuthor Info & Affiliations
Circulation
Volume 99, Number 12
https://doi.org/10.1161/01.CIR.99.12.1593
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Abstract

Background—Pulmonary endothelium has metabolic functions including the conversion of angiotensin I to angiotensin II by angiotensin-converting ectoenzyme (ACE). In this study, we have validated an indicator-dilution technique that provides estimations of dynamically perfused capillary surface area (DPCSA) in humans, and we have characterized pulmonary endothelial ACE in vivo.
Methods and Results—In 12 adults, single-pass transpulmonary (one or both lungs) hydrolysis of the specific ACE substrate 3H-benzoyl-Phe-Ala-Pro (3H-BPAP) was measured and expressed as % metabolism (%M) and v=−ln(1−M). We also calculated Amax/Km, an index of DPCSA. %M (70.1±3.2 vs 67.9±3.1) and v (1.29±0.14 vs 1.20±0.12) were similar in both lungs and the right lung, respectively, whereas Amax/Km//body surface area decreased from 2460±193 to 1318±115 mL/min per square meter.
Conclusions—Pulmonary endothelial ACE activity can be assessed in humans at the bedside by means of indicator-dilution techniques. Our data suggest homogeneous pulmonary capillary ACE concentrations and capillary transit times (tc) in both human lungs, and similar tc within the normal range of cardiac index. Amax/Km in the right lung is 54% of total Amax/Km in both lungs, suggesting that Amax/Km is a reliable and quantifiable index of DPCSA in humans.
The pulmonary vascular endothelium participates in important physiological and pharmacokinetic processes, including synthesis and degradation of vasoactive peptides.1 2 Ectoenzymes responsible for these functions are located on the luminal surface of the endothelium.3 Because these enzymes are directly accessible to blood-borne substrates, their activities may be measured in vivo by means of indicator-dilution techniques.4 5 6 In humans, endothelium-bound angiotensin-converting enzyme (ACE; kininase II; EC 3.4.15.1) is responsible for the conversion of angiotensin I to angiotensin II and for bradykinin inactivation and is thus a major regulator of blood pressure in health and disease.3
Pulmonary endothelial ACE activity may be assessed in vivo by monitoring the hydrolysis of a synthetic substrate in plasma during a single passage through the lungs.5 Unlike natural angiotensin I and bradykinin, synthetic substrates of ACE do not alter vessel tone and are not metabolized by other endogenous peptidases and when hydrolyzed by ACE yield products that are easily separated from the parent compound by organic extraction.6 The first and most widely used ACE substrate to date is the highly specific tripeptide benzoyl-Phe-Ala-Pro (BPAP).6
ACE molecules are uniformly distributed along the luminal pulmonary endothelial surface, including the membrane caveolae,3 suggesting that in addition to its biological activity, pulmonary capillary endothelium-bound ACE (PCEB-ACE) may be a useful indicator of endothelial function and allow estimation of the perfused capillary surface area under physiological conditions.2 5 7 Moreover, PCEB-ACE dysfunction is an early and sensitive index of lung vascular injury.8 9 Thus monitoring of PCEB-ACE activity in humans might be used to estimate changes in perfused capillary surface area, to quantify the degree of endothelial dysfunction, and as a biochemical marker to identify early vascular lung injury.
In this study, we have for the first time validated the PCEB-ACE indicator-dilution technique at the bedside with human subjects and correlated it with pulmonary hemodynamics to identify patterns of PCEB-ACE activity under normal lung conditions and obtain insights into human pulmonary endothelial physiology and pharmacology.

Methods

Subjects

Twelve volunteers, 9 men and 3 women (age 34 to 79 years, body surface area [BSA] 1.5 to 2.1 m2), without pulmonary disease or heart failure and undergoing cardiac catheterization for coronary artery disease assessment, participated in a protocol approved by the Research Ethics Committee. Written informed consent was obtained. They were not receiving ACE inhibitor treatment. No patient had an anatomic shunt or patent foramen ovale detectable by 2-dimensional Doppler echocardiography by use of agitated saline as a contrast agent.
Femoral venous and femoral arterial sheaths were inserted as part of the routine cardiac catheterization procedure. A 5-lumen 8F thermodilution catheter (Abbott) was advanced into the pulmonary artery. Cardiac output was measured by the thermodilution technique.
For estimation of the single-pass transpulmonary hydrolysis of 3H-BPAP, all patients received 2 rapid bolus injections through the pulmonary artery catheter, 10 minutes apart. In injection A (both lungs), the bolus was injected through the proximal port of the catheter into the right atrium and was thus distributed throughout the vascular bed of both lungs. In injection B (one lung), the bolus was injected through the distal port of the catheter into either the left or the right main pulmonary artery and was carried with the blood flow into the entire vascular bed of one lung, as confirmed by angiographic dye injection and fluoroscopy. In all but 1 subject (No. 5), the distal end of the catheter had passed into the right pulmonary artery. The order of injections was randomly selected before the beginning of each patient study. Cardiac output (CO) was determined immediately before each injection. Blood flow to one lung was estimated as 53% of the corresponding CO when the injection was made into the right pulmonary artery (all subjects except subject 5, see Table) and as 47% of the corresponding CO of subject 5, in whom the injection was made into the left pulmonary artery.10
To validate our method and to provide a basis for comparison, 9 other patients with precapillary pulmonary hypertension (primary pulmonary hypertension, 2; collagen disease, 3; anorexigen-related, 1; repaired atrial septal defect, 1; sarcoidosis, 2; age range 22 to 68 years, mean pulmonary artery pressure 47.2±13.5 mm Hg) were also studied. These patients had a single injection of substrate into the right atrium, distributed to both lungs.

Determination of Pulmonary Endothelial ACE Activity

One milliliter of a solution of 3H-BPAP (30 μCi/1.2 mL 0.9% saline; 22.2 Ci/mmol) was used for each injection, followed by a 5-mL saline flush. Simultaneously, arterial blood was withdrawn through the femoral artery sheath (40 mL/min, Coleman Instruments peristaltic pump) into a fraction collector (Gilson), advancing at 1 tube per 1.2 seconds (0.8 mL blood/tube, 39 tubes). The tubes contained 1.75 mL of normal saline with 5 mmol/L EDTA and 6.8 mmol/L 8-hydroxyquinoline 5-sulfonic acid to prevent further activity of blood ACE and heparin 1000 IU/L. After centrifugation (3000 rpm, 10 minutes), 0.5 mL of the supernatant was transferred into a scintillation vial containing 5 mL Ecolite, and total 3H radioactivity was measured (3H total). For the determination of the radioactivity associated with metabolites, another 0.5 mL of the supernatant was transferred into a scintillation vial containing 2.5 mL HCl (0.12N). After addition of 3 mL of 0.4% Omnifluor in toluene and mixing by inversion, the radioactivity (3H toluene) was measured after 48 hours of undisturbed equilibration in the dark. With this technique, ≈60% of the 3H-BPAP metabolite 3H-Benzoyl-Phe (3H-BPhe, fp) and <10% of the parent 3H-BPAP (fs) were extracted in the organic phase of the mixture (ie, toluene). The precise values were calculated by identically processing separate standard tubes containing substrate or previously synthesized product.
After correcting for background radioactivity, radioactivity from the product 3H-BPhe was calculated as
\[^{\mathrm{3}}\mathrm{H-BPhe{=}(}^{\mathrm{3}}\mathrm{H\ toluene-f}_{\mathrm{s}}\mathrm{{\times}}^{\mathrm{3}}\mathrm{H\ total)/(f}_{\mathrm{p}}\mathrm{-f}_{\mathrm{s}}\mathrm{)}\]
where fs and fp are the fractional extractions of substrate (3H-BPAP) and product (3H-BPhe), respectively, into the toluene layer.

Calculations of ACE Activity Parameters

Under first-order reaction conditions ([S]≪Km), the Henri-Michaelis-Menten equation becomes11
\[\mathrm{-d{[}S{]}/dt{=}V{=}(V}_{\mathrm{max}}\mathrm{/K}_{\mathrm{m}}\mathrm{){\times}{[}S{]}}\]
with Km, V, and Vmax being the Michaelis-Menten constant, the reaction velocity, and maximal velocity, respectively. Because of the minimal contribution of both the extracapillary endothelium-bound9 and the plasma soluble ACE to substrate conversion,9 the reaction time is in practical terms equal to tc (ie, capillary transit time). By integrating from time 0 to tc and from [S0] (ie, initial substrate concentration) to [S] (ie, surviving substrate concentration at time t) and rearranging,
\[\mathrm{V}_{\mathrm{max}}\mathrm{/K}_{\mathrm{m}}\mathrm{{\times}t}_{\mathrm{c}}\mathrm{{=}ln({[}S}_{\mathrm{o}}\mathrm{{]}/{[}S{]})}\]
since by definition Vmax=[E]×kcat, Equation 3 becomes
\[\mathrm{{[}E{]}{\times}t}_{\mathrm{c}}\mathrm{{\times}k}_{\mathrm{cat}}\mathrm{/K}_{\mathrm{m}}\mathrm{{=}ln({[}S}_{\mathrm{o}}\mathrm{{]}/{[}S{]}){=}v}\]
with [E] and kcat being the capillary enzyme concentration and catalytic rate constant, respectively. [So] and [S] reflect the initial and final substrate concentrations in the effluent arterial plasma estimated in dpm/mL, where [So] is [3H-BPAP]+[3H-BPhe] and [S] is the surviving substrate concentration, that is, [3H-BPAP]. Expressing 3H-BPAP hydrolysis as v has the advantage of being directly proportional to the 3 kinetic parameters that determine enzyme activity.8 Equation 4 applies when all enzyme molecules are equally reactive. Since BPAP exists in 2 different conformational forms (cis and trans)12 with the cis isomer being nonreactive, Equation 4 was further modified to the applied Equation 57 13 to incorporate the nonreactive fraction (nrf=7%) of BPAP13 :
\[\mathrm{v{=}ln{\{}(1-nrf)/(({[}S{]}/{[}S}_{\mathrm{o}}\mathrm{{]})-nrf){\}}{=}{[}E{]}{\times}t}_{\mathrm{c}}\mathrm{{\times}k}_{\mathrm{cat}}\mathrm{/K}_{\mathrm{m}}\]
We additionally calculated the percent transpulmonary 3H-BPAP metabolism (%M),14 which was also corrected for the cis isomer nonreactive fraction:
\[\mathrm{\%M{=}100{\times}{\{}({[}S}_{\mathrm{o}}\mathrm{{]}-{[}S{]})/({[}S}_{\mathrm{o}}\mathrm{{]}{\times}(1-nrf)){\}}}\]
Data were further analyzed with the use of the integrated Henri-Michaelis-Menten equation as modified by Catravas and White14 :
\[\mathrm{A}_{\mathrm{max}}\mathrm{/K}_{\mathrm{m}}\mathrm{{=}E{\times}k}_{\mathrm{cat}}\mathrm{/K}_{\mathrm{m}}\mathrm{{=}F}_{\mathrm{p}}\mathrm{{\times}v}\]
where
\[\mathrm{A}_{\mathrm{max}}\mathrm{{=}E{\times}k}_{\mathrm{cat}}\mathrm{{=}V}_{\mathrm{max}}\mathrm{{\times}Q}_{\mathrm{cap}}\]
with E, Fp, and Qcap being total enzyme mass, pulmonary plasma flow (=CO×[1−Hct]), and capillary plasma volume, respectively. Since kcat/Km is the second-order rate constant, Amax/Km is proportional to the available enzyme mass and hence to the surface area of the perfused capillary vascular bed.5 7
Mean 3H transit time (¯t) and volume of 3H distribution (Q3H) for the substrate were calculated as
\[\mathrm{{\bar}t{=}}\ {\int_{o}^{t}}t{[}S_{o}{]}dt\left/{\int_{o}^{t}}{[}S_{o}{]}dt\right.\]
and
\[\mathrm{Q}_{\mathrm{3H}}\mathrm{{=}F}_{\mathrm{p}}\mathrm{{\times}{\bar}t}\]
where ¯t calculations were corrected for catheter transit time.

Statistics

Data are presented as mean±SEM. To compare means and individual values, the paired t test, Student’s t test, and Pearson r test were used where appropriate. Correlations were determined with the use of least-squares linear regression. A value of P<0.05 was considered significant.

Results

All subjects (Table) had atherosclerotic coronary artery disease with the exception of subject 2, who had a normal coronary angiogram. Cardiac indexes (CI), arterial blood pH, Pco2, and Po2 values were within the normal range.
Representative arterial outflow concentration curves of total-3H and the surviving 3H-BPAP after a single passage through both lungs and the corresponding hydrolysis (v) of 3H-BPAP by ACE are presented in Figure 1. Sample-to-sample substrate hydrolysis (v) fluctuates slightly around 1.47, denoting that in this particular individual, ≈77% of the injected BPAP was metabolized to BPhe.

ACE Activity in One Versus Both Lungs

No differences were observed between injections A (both lungs) and B (one lung) in CO (5.73±0.28 vs 6.21±0.34 L/min, respectively) or Fp (3.62±0.20 vs 3.91±0.22 L/min). There were no differences (Figure 2) in either 3H-BPAP %M (70.1±3.2% vs 67.9±3.1%) or v (1.29±0.14 vs 1.20±0.12), whereas a 46% reduction occurred in Amax/Km when 3H-BPAP was injected into the right lung (2449±249 mL/min) versus both lungs (4564±425, P<0.01). An identical 46% difference was observed between the right lung and both lungs when Amax/Km values were normalized to the BSA of each subject (2460±193 vs 1318±115 mL/min per square meter, P<0.01).

ACE Activity and Hemodynamics in Both Lungs

As Amax/Km/BSA (Figure 3) increased from 1639 to 3793 mL/min per square meter, 3H-BPAP %M increased linearly from 57.9% to 91.7%, with a strong positive correlation between the two parameters (r=0.89, P<0.01).
3H-BPAP %M and v (Figure 4) correlated inversely with mean pulmonary artery pressure (mPAP) (r=0.68, P<0.05 and r=0.644, P<0.05, respectively), whereas Amax/Km/BSA was not related to mPAP (r=0.42, P=NS). In addition, 3H-BPAP transpulmonary hydrolysis expressed as %M and v, as well as Amax/Km/BSA, were independent of both CI and pulmonary vascular resistance index (PVRI). The independence of Amax/Km/BSA versus mPAP, CI, and PVRI was maintained even when Amax/Km was not normalized to BSA (data not shown). Similar patterns were observed in the aforementioned relations when the enzyme activity parameters were plotted against PVR instead of PVRI (data not shown).
There was a trend toward a negative linear relation between transit time and CI (Figure 5, r=0.51). There was no correlation between Q3H and CI (r=0.17).

Patients with Pulmonary Hypertension

In the pulmonary hypertension patient group (Figure 6), mean values for %M (37%±9%), v (0.47±0.13), and Amax/Km/BSA (641±297) were markedly reduced as compared with the 12 subjects with normal pulmonary arterial pressures (P<0.01 in all cases).

Discussion

In this study, pulmonary endothelium–bound ACE activity and mass have been estimated in vivo and correlated with pulmonary hemodynamic parameters in the normal human lung. We also present data from patients with pulmonary hypertension for comparison purposes. ACE function was assessed with indicator-dilution techniques and study of the transpulmonary utilization of the synthetic ACE substrate BPAP. PCEB-ACE dysfunction has been an early and sensitive finding in animal models of lung injury,8 9 and, under physiological conditions, PCEB-ACE assays estimate enzyme mass5 and perfused vascular surface area.7 15 Although ACE is present on all endothelial cells, microvessels, principally capillaries, are responsible for the great majority of single-pass transpulmonary hydrolysis,9 whereas the contribution of plasma ACE is minimal.9 Thus in our studies, measurement of pulmonary ACE activity represents in practical terms PCEB-ACE activity. ACE inhibitors inhibit endothelium-bound ACE,16 and our subjects were carefully questioned about ACE inhibitor usage. Binding of BPAP to serum albumen would also affect the assay.17 However, BPAP binding by albumen does not necessarily predict similar binding by native serum proteins, and serum protein binding of BPAP does not appear to be a factor limiting BPAP hydrolysis in vivo.18
The sample-to-sample variability in BPAP hydrolysis (Figure 1) reflects ACE activity within individual groups of capillaries and may be influenced by substrate transit time, enzyme concentration, and the enzyme kinetic constants, as in Equation 5. The pattern observed suggests the presence of mild heterogeneity in capillary transit times, since capillary enzyme concentrations and ACE catalytic properties should remain unchanged.
The lack of difference in 3H-BPAP hydrolysis or %M between one and both lungs (Figure 2) indicates homogeneous PCEB-ACE activity between the two lungs. The relatively wide range of individual values may be explained in part by greater population heterogeneity in humans than the average, typically inbred, animal group. PCEB-ACE activity was independent of age (data not shown). Our patients had coronary atherosclerosis, and this might have contributed to the variability, since endothelial dysfunction, an early feature of atherosclerosis, might also affect the lung circulation. Hyperlipidemia might also contribute.19 However, there was no overt evidence of pulmonary vascular disease as assessed by hemodynamics. Subject 2 in our study had angiographically normal coronary arteries, yet her data were similar to the rest of the group. Furthermore, PCEB-ACE activity in healthy lung donors20 and patients with lung carcinoma,21 conditions in which pulmonary endothelial dysfunction is less likely, is similar to that of our coronary disease group. Thus as in other studies,22 23 our “normal” population with coronary disease presents a standard to be used in future studies of patients with lung dysfunction. By comparison, our patients with pulmonary vascular disease had markedly reduced PCEB-ACE activity.
3H-BPAP %M and v were independent of CI, consistent with similar capillary transit times among individuals within the normal range of pulmonary blood flow at rest.3 H-BPAP hydrolysis, expressed as %M and v, decreased with increasing mPAP values. This negative correlation might be related to subtle endothelial dysfunction from the atherosclerosis in our population, manifested by a slight rise in PAP and causing mild decreases in PCEB-ACE activity. The mPAP reflects systolic characteristics of the large pulmonary arteries and diastolic microvascular resistance, representing the pressure characteristics of the entire lung circulation. There was no relation of %M with PVRI. However, PVRI is a derived value (mPAP−PAWP [mean pulmonary artery wedge pressure])/CI. Because 3H-BPAP metabolism was independent of CI, it would also be independent of the calculated PVRI regardless of any relation between %M and mPAP.
Amax/Km has been used as an index of PCEB-ACE mass and consequently dynamically perfused capillary surface area (DPCSA).5 6 7 This assumption is based on Equation 7: when kcat and Km remain constant, changes in Amax/Km reflect changes in E (ie, enzyme mass). For enzymes evenly distributed along the luminal endothelial surface, such as ACE, changes in E should reflect changes in DPCSA. Under normal conditions, kcat and Km are not affected by changes in flow and do remain constant.2 5 Amax/Km is an index of DPCSA only (ie, capillaries through which blood is flowing allowing substrate-enzyme interaction) and not of capillaries that are nonperfused or transiently filled with “stagnant” blood.
Amax/Km and Amax/Km/BSA were reduced by 46% when 3H-BPAP was injected into the right lung instead of both lungs (Figure 2). No change in CO, which could contribute to this decrease, was noted between the two injections. There was an almost identical pattern between Amax/Km values obtained in the right lung, being 54% of those obtained in both lungs, and the corresponding fraction of lung perfusion reported in supine humans (53% to the right lung and 47% to the left).10 Amax/Km thus appears to be a sensitive and quantifiable DPCSA index in humans, as it is in other animals. We used Amax/Km/BSA because, unlike experimental animal groups, human populations have great variability in BSA and consequently in lung capillary surface area. Normalizing Amax/Km to BSA reveals the homogeneity of the human population (Figure 2), allowing better comparisons of different human groups in future studies. Amax/Km/BSA has been shown to be a sensitive index of DPCSA changes induced by cardiac output elevations in humans.24
It has been suggested that Amax/Km cannot be used as a quantitative index of perfused capillary surface area because of the presence of the nonreactive cis isomer BPAP fraction.15 25 This fraction was estimated to be ≈15% in buffer solution,26 whereas in vivo it appears to represent 7% of all BPAP,13 probably because of the presence of natural isomerases in plasma. However, studies done with different substrates concurrently injected, or correcting for the nonreactive fraction, confirm that Amax/Km is a quantifiable index of perfused lung capillaries.5 7 13
Assessing PCEB-ACE activity in humans with pulmonary vascular pathologies, such as acute lung injury–adult respiratory distress syndrome or pulmonary hypertension, may help distinguish between abnormalities secondary to endothelial dysfunction per se and decreased pulmonary vascular surface area. If endothelial dysfunction is related either to decreased enzyme mass and consequently decreased enzyme concentrations or to kinetic constant alteration, then substrate hydrolysis would be altered (Equation 5). In such a case, Amax/Km should be viewed as an index of functional capillary surface area, related to both enzyme quantity and functional integrity. The data from our 9 patients with precapillary pulmonary hypertension show decreased substrate hydrolysis and Amax/Km, suggesting some combination of endothelial dysfunction and loss of DPCSA. If, on the other hand, loss of DPCSA occurs with neither endothelial dysfunction nor changes in capillary transit times, substrate hydrolysis would remain unchanged, whereas Amax/Km would decrease, since the enzyme mass available for reaction would be decreased (Equation 7). Dupuis et al27 28 have provided evidence that the DPCSA available for ACE substrate reaction and norepinephrine and serotonin uptake increases during exercise in dogs in a parallel fashion, which confirms the consistency and validity of the techniques and demonstrates capillary recruitment. Similar studies should be performed in exercising normal humans. Moreover, a failure to increase DPCSA during exercise might prove to be an early and subtle marker of pulmonary vascular disease.
Mean 3H transit time is an approximation of mean lung transit time because it also includes the time needed for the blood to travel from the left atrium to the tip of the femoral arterial sheath. Similar considerations apply to the volume of 3H distribution. The trend toward a negative correlation among ¯t and CI (Figure 5) confirms that the transpulmonary passage of the probe tends to be quicker when CI is higher. The fact that the CI-related decreases in ¯t are combined with unchanged 3H-BPAP %M and v suggests that higher cardiac outputs are accommodated through recruitment of unperfused capillaries with similar tc. The absence of correlation among Q3H and CI may relate to differences in lung blood volume and subsequently Q3H being blunted by BSA normalizations within the range of normal resting pulmonary blood flows. In fact, when Q3H is plotted against CO, the pattern becomes more linear (data not shown) Additional factors may be the differences in hematocrit and the plasma volume inside the aorta.
In summary, our studies demonstrate that pulmonary endothelial ACE activity may be assessed in humans at the bedside by means of indicator-dilution techniques and that it provides a reliable and quantifiable index of DPCSA. Our data establish the metabolic activity values for humans without overt pulmonary vascular disease. Studies performed with other markers, such as the clearance of prostaglandin E1, norepinephrine, propranolol, serotonin, and endothelin-1, have contributed greatly to the understanding of normal pulmonary endothelial function and of endothelial dysfunction in various pulmonary vascular diseases.4 22 23 27 28 With the use of the techniques we describe, the assessment of PCEB-ACE activity in these and other disease states will further our understanding of pulmonary vascular metabolism and pathophysiology.
Figure 1. Femoral arterial plasma concentration curves of total tritium (3H, •) and 3H-BPAP (▪) after injection into the right atrium of a representative male subject. BPAP hydrolysis (v, ♦) was estimated from samples in which total radioactivity dpm >10×background dpm.
Figure 2. Transpulmonary BPAP %M and BPAP hydrolysis (v) through both and one lung (left) and corresponding Amax/Km given in absolute values and normalized per BSA (Amax/Km/BSA, right). Individual values and corresponding mean±SEM values are shown. Each subject is represented by a different symbol given in the Table. **P<0.01 vs both lungs.
Figure 3. Correlation of individual Amax/Km/BSA values with corresponding BPAP %M in the 12 subjects.
Figure 4. Relations of mPAP (left), CI (center), and PVRI (right) with BPAP %M (top) and with v (middle) and plot of mPAP with Amax/Km/BSA (bottom) in the 12 study subjects. Lines denote significant linear relation. r, Pearson r value.
Figure 5. Top, Plot of 3H transit time with CI. Bottom, Plot of volume of 3H distribution with CI. Symbols as in Figure 4.
Figure 6. BPAP %M, v, and Amax/Km/BSA in 9 patients with precapillary pulmonary hypertension.
Table 1. Characteristics and Hemodynamic Parameters of the 12 Study Volunteers
SubjectSymbolAge, ySexHctSAP, mm Hg PAP, mm Hg PAWP; TPG, mm HgCI, L · min−1 · m−2PVRI, dyne · s−1 · cm−5 · m−2
     Sys/DiasMeanSys/DiasMean   
1+71M0.384106 /566718 /494; 52.61153.1
2Δ34F0.377140 /709331 /101710; 73.30169.5
3○44M0.372105 /708227 /101610; 63.25147.5
4✚58M0.403140 /769719 /101310; 33.4170.3
5▴52M0.378188 /8011620 /10134; 92.55282
6•62F0.365150 /709739 /192519; 63.39141.4
7▿55M0.368108 /668020 /8128; 42.86111.8
8⋄74F0.313135 /608535 /182415; 92.73263.4
9□58M0.421118 /658320 /494; 52.64151.3
10♦43M0.366138 /759637 /162315; 83.49183.2
11▪48M0.38134 /668934 /142113; 83.38189.1
12⊕79M0.305138 /588537 /10195; 143.77296.7
Hct indicates hematocrit; SAP, systemic arterial pressure; PAP, pulmonary arterial pressure; Sys, systolic; Dias, diastolic; PAWP, mean pulmonary artery wedge pressure; TPG, transpulmonary gradient (mPAP−PAWP); CI, cardiac index; and PVRI, pulmonary vascular resistance index. Symbols represent each patient shown in Figure 2.

Acknowledgments

This study was supported by Fonds de la Recherche en Santé du Quebec (Dr Langleben, Chercheur-Boursier Clinicien), the Thorax Foundation, the European Union and the Greek General Secretariat of Research and Technology-PENED 1997, and the National Institutes of Health (HL-31422).

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Published In

Go to Circulation
Circulation
Volume 99 • Number 12 • 30 March 1999
Pages: 1593 - 1599
PubMed: 10096936

Copyright

Copyright © 1999 by American Heart Association.

History

Received: 22 September 1998
Revision received: 20 November 1998
Accepted: 18 December 1998
Published online: 30 March 1999
Published in print: 30 March 1999

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Keywords

  1. lung
  2. endothelium
  3. circulation
  4. angiotensin
  5. enzymes
  6. hypertension, pulmonary

Authors

Affiliations

Stylianos E. Orfanos
MD, PhD
From the Division of Cardiology, Jewish General Hospital, McGill University, Montreal, Canada (S.E.O., D.L., J.K., R.D.S., L.D.); the Critical Care Department, Evangelismos Hospital, University of Athens Medical School, Athens, Greece (S.E.O., C.R.); and the Vascular Biology Center, Medical College of Georgia, Augusta (J.W.R., J.D.C.).
View all articles by this author
David Langleben
MD
From the Division of Cardiology, Jewish General Hospital, McGill University, Montreal, Canada (S.E.O., D.L., J.K., R.D.S., L.D.); the Critical Care Department, Evangelismos Hospital, University of Athens Medical School, Athens, Greece (S.E.O., C.R.); and the Vascular Biology Center, Medical College of Georgia, Augusta (J.W.R., J.D.C.).
View all articles by this author
Joseph Khoury
MSc
From the Division of Cardiology, Jewish General Hospital, McGill University, Montreal, Canada (S.E.O., D.L., J.K., R.D.S., L.D.); the Critical Care Department, Evangelismos Hospital, University of Athens Medical School, Athens, Greece (S.E.O., C.R.); and the Vascular Biology Center, Medical College of Georgia, Augusta (J.W.R., J.D.C.).
View all articles by this author
Robert D. Schlesinger
MD
From the Division of Cardiology, Jewish General Hospital, McGill University, Montreal, Canada (S.E.O., D.L., J.K., R.D.S., L.D.); the Critical Care Department, Evangelismos Hospital, University of Athens Medical School, Athens, Greece (S.E.O., C.R.); and the Vascular Biology Center, Medical College of Georgia, Augusta (J.W.R., J.D.C.).
View all articles by this author
Leonidas Dragatakis
MD
From the Division of Cardiology, Jewish General Hospital, McGill University, Montreal, Canada (S.E.O., D.L., J.K., R.D.S., L.D.); the Critical Care Department, Evangelismos Hospital, University of Athens Medical School, Athens, Greece (S.E.O., C.R.); and the Vascular Biology Center, Medical College of Georgia, Augusta (J.W.R., J.D.C.).
View all articles by this author
Charis Roussos
MD, PhD
From the Division of Cardiology, Jewish General Hospital, McGill University, Montreal, Canada (S.E.O., D.L., J.K., R.D.S., L.D.); the Critical Care Department, Evangelismos Hospital, University of Athens Medical School, Athens, Greece (S.E.O., C.R.); and the Vascular Biology Center, Medical College of Georgia, Augusta (J.W.R., J.D.C.).
View all articles by this author
James W. Ryan
MD, DPhil
From the Division of Cardiology, Jewish General Hospital, McGill University, Montreal, Canada (S.E.O., D.L., J.K., R.D.S., L.D.); the Critical Care Department, Evangelismos Hospital, University of Athens Medical School, Athens, Greece (S.E.O., C.R.); and the Vascular Biology Center, Medical College of Georgia, Augusta (J.W.R., J.D.C.).
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John D. Catravas
PhD
From the Division of Cardiology, Jewish General Hospital, McGill University, Montreal, Canada (S.E.O., D.L., J.K., R.D.S., L.D.); the Critical Care Department, Evangelismos Hospital, University of Athens Medical School, Athens, Greece (S.E.O., C.R.); and the Vascular Biology Center, Medical College of Georgia, Augusta (J.W.R., J.D.C.).
View all articles by this author

Notes

Correspondence to Dr David Langleben, Division of Cardiology, Jewish General Hospital, 3755, Chemin de la Cote Ste-Catherine, Room E-258, Montreal, P.Q. H3T 1E2, Canada. E-mail [email protected]

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Pulmonary Capillary Endothelium-Bound Angiotensin-Converting Enzyme Activity in Humans
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