Density-dependent reduction of nitric oxide diffusing capacity after pneumonectomy

2003 ◽  
Vol 94 (5) ◽  
pp. 1926-1932 ◽  
Author(s):  
Connie C. W. Hsia ◽  
Xiao Yan ◽  
D. Merrill Dane ◽  
Robert L. Johnson

Airway lengthening after pneumonectomy (PNX) may increase diffusive resistance to gas mixing (1/DG); the effect is accentuated by increasing acinar gas density but is difficult to detect from lung CO-diffusing capacity (Dl CO). Because lung NO-diffusing capacity (Dl NO) is three- to fivefold that of Dl CO, whereas 1/DG for NO and CO are similar, we hypothesized that a density-dependent fractional reduction would be greater for Dl NO than for Dl CO. We measured Dl NOand Dl CO at two tidal volumes (Vt) and with three background gases [helium (He), nitrogen (N2), and sulfur hexafluoride (SF6)] in immature dogs 3 and 9 mo after right PNX (5 and 11 mo of age). At maturity (11 mo), background gas density had no effect on Dl NO, Dl CO, or Dl NO-to-Dl CO ratio in sham controls. In PNX animals, Dl NO declined 25–50% in SF6 relative to He and N2, and Dl NO/Dl CO declined ∼50% in SF6 relative to He at a Vt of 15 ml/kg, consistent with a significant 1/DG. At 5 mo of age, Dl NO/Dl CO declined 25–45% in SF6 relative to He and N2 in both groups, but Dl CO increased paradoxically in SF6 relative to N2 or He by 20–60%. Findings suggest that SF6, besides increasing 1/DG, may redistribute ventilation and/or enhance acinar penetration of the convective front.

2014 ◽  
Vol 116 (1) ◽  
pp. 32-41 ◽  
Author(s):  
Colin Borland ◽  
Fiona Bottrill ◽  
Aled Jones ◽  
Chris Sparkes ◽  
Alain Vuylsteke

The lung nitric oxide (NO) diffusing capacity (DlNO) mainly reflects alveolar-capillary membrane conductance (Dm). However, blood resistance has been shown in vitro and in vivo. To explore whether this resistance lies in the plasma, the red blood cell (RBC) membrane, or in the RBC interior, we measured the NO diffusing capacity (Dno) in a membrane oxygenator circuit containing ∼1 liter of horse or human blood exposed to 14 parts per million NO under physiological conditions on 7 separate days. We compared results across a 1,000-fold change in extracellular diffusivity using dextrans, plasma, and physiological salt solution. We halved RBC surface area by comparing horse and human RBCs. We altered the diffusive resistance of the RBC interior by adding sodium nitrite converting oxyhemoglobin to methemoglobin. Neither increased viscosity nor reduced RBC size reduced Dno. Adding sodium nitrite increased methemoglobin and was associated with a steady fall in Dno ( P < 0.001). Similar results were obtained at NO concentrations found in vivo. The RBC interior appears to be the site of the blood resistance.


2009 ◽  
Vol 103 (12) ◽  
pp. 1892-1897 ◽  
Author(s):  
I. van der Lee ◽  
H.A. Gietema ◽  
P. Zanen ◽  
R.J. van Klaveren ◽  
M. Prokop ◽  
...  

1982 ◽  
Vol 53 (4) ◽  
pp. 930-939 ◽  
Author(s):  
M. F. Petrini ◽  
B. T. Peterson ◽  
R. W. Hyde ◽  
V. Lam ◽  
M. J. Utell ◽  
...  

To evaluate the rate of gas mixing in human lungs during rebreathing maneuvers used to measure pulmonary tissue volume (Vt) and pulmonary capillary blood flow (Qc), we devised a method to determine the dead space during rebreathing (VRD). Required measurements are initial concentration of a foreign inert insoluble gas in the rebreathing bag, first mixed expired concentration, equilibrated concentration, volume inspired, and volume of the first expired breath. In subjects breathing rapidly at 30 breaths/min with inspired volumes in excess of 2 liters, VRD had values three or more times greater than the predicted anatomical dead space (VD). Breath holding after the first inspiration progressively diminished VRD so that after 10–15 s, it approximately equaled predicted VD. VRD measured with helium was smaller than VRD measured with sulfur hexafluoride. The reported degree of uneven ventilation from gravitational forces in normal humans can account for only about one-third of the difference between VRD and VD. These findings support the concept that mixing by diffusion between peripheral parallel airways is incomplete at normal breathing rates in humans and can result in errors as high as 25% in Vt and Qc.


2019 ◽  
Vol 5 (2) ◽  
pp. 00260-2018 ◽  
Author(s):  
Martina Nassif ◽  
Reindert P. van Steenwijk ◽  
Ivo van der Lee ◽  
Peter J. Sterk ◽  
Frans H.C. de Jongh ◽  
...  

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