Nitric oxide synthesis in the lung. Regulation by oxygen through a kinetic mechanism.

RA Dweik, D Laskowski, HM Abu-Soud… - The Journal of …, 1998 - Am Soc Clin Investig
RA Dweik, D Laskowski, HM Abu-Soud, F Kaneko, R Hutte, DJ Stuehr, SC Erzurum
The Journal of clinical investigation, 1998Am Soc Clin Investig
In this study, we show that oxygen regulates nitric oxide (NO) levels through effects on NO
synthase (NOS) enzyme kinetics. Initially, NO synthesis in the static lung was measured in
bronchiolar gases during an expiratory breath-hold in normal individuals. NO accumulated
exponentially to a plateau, indicating balance between NO production and consumption in
the lung. Detection of NO2-, NO3-, and S-nitrosothiols in lung epithelial lining fluids
confirmed NO consumption by chemical reactions in the lung. Interestingly, alveolar gas NO …
In this study, we show that oxygen regulates nitric oxide (NO) levels through effects on NO synthase (NOS) enzyme kinetics. Initially, NO synthesis in the static lung was measured in bronchiolar gases during an expiratory breath-hold in normal individuals. NO accumulated exponentially to a plateau, indicating balance between NO production and consumption in the lung. Detection of NO2-, NO3-, and S-nitrosothiols in lung epithelial lining fluids confirmed NO consumption by chemical reactions in the lung. Interestingly, alveolar gas NO (estimated from bronchiolar gases at end-expiration) was near zero, suggesting NO in exhaled gases is not derived from circulatory/systemic sources. Dynamic NO levels during tidal breathing in different airway regions (mouth, trachea, bronchus, and bronchiole) were similar. However, in individuals breathing varying levels of inspired oxygen, dynamic NO levels were notably dependent on O2 concentration in the hypoxic range (KmO2 190 microM). Purified NOS type II enzyme activity in vitro was similarly dependent on molecular oxygen levels (KmO2 135 microM), revealing a means by which oxygen concentration affects NO levels in vivo. Based upon these results, we propose that NOS II is a mediator of the vascular response to oxygen in the lung, because its KmO2 allows generation of NO in proportion to the inspired oxygen concentration throughout the physiologic range.
The Journal of Clinical Investigation