Effective diffusion distance of nitric oxide in the microcirculation
Departments of 1 Chemical Engineering and 2 Medical Physiology, Texas A & M University, College Station, Texas 77843; and 3 Department of Chemical Engineering, University of California, Los Angeles, California 90095-1592 Despite its well-documented importance, the mechanism for nitric oxide (...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 1998-05, Vol.274 (5), p.H1705-H1714 |
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Zusammenfassung: | Departments of 1 Chemical
Engineering and 2 Medical
Physiology, Texas A & M University, College Station, Texas 77843;
and 3 Department of Chemical
Engineering, University of California, Los Angeles, California
90095-1592
Despite its well-documented importance, the
mechanism for nitric oxide (NO) transport in vivo is still unclear. In
particular, the effect of hemoglobin-NO interaction and the range of NO
action have not been characterized in the microcirculation, where blood flow is optimally regulated. Using a mathematical model and
experimental data on NO production and degradation rates, we
investigated factors that determine the effective diffusion distance of
NO in the microcirculation. This distance is defined as the distance
within which NO concentration is greater than the equilibrium
dissociation constant (0.25 µM) of soluble guanylyl cyclase, the
target enzyme for NO action. We found that the size of the vessel is an
important factor in determining the effective diffusion distance of NO.
In ~30- to 100-µm-ID microvessels the luminal NO concentrations and
the abluminal effective diffusion distance are maximal. Furthermore,
the model suggests that if the NO-erythrocyte reaction rate is as fast
as the rate reported for the in vitro NO-hemoglobin reaction, the NO
concentration in the vascular smooth muscle will be insufficient to
stimulate smooth muscle guanylyl cyclase effectively. In addition, the
existence of an erythrocyte-free layer near the vascular wall is
important in determining the effective NO diffusion distance. These
results suggest that 1 ) the range of
NO action may exhibit significant spatial heterogeneity in vivo,
depending on the size of the vessel and the local chemistry of NO
degradation, 2 ) the NO
binding/reaction constant with hemoglobin in the red blood cell may be
much smaller than that with free hemoglobin, and
3 ) the microcirculation is the
optimal site for NO to exert its regulatory function. Because NO
exhibits vasodilatory function and antiatherogenic activity, the high
NO concentration and its long effective range in the microcirculation
may serve as intrinsic factors to prevent the development of systemic
hypertension and atherosclerotic pathology in microvessels.
mathematical model; reaction kinetics; hemoglobin; endothelium; mass transport |
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ISSN: | 0363-6135 0002-9513 1522-1539 |
DOI: | 10.1152/ajpheart.1998.274.5.H1705 |