Cited by 82Nitric Oxide and Endothelin EffectsCardiovascular Health and Disease PreventionRedox biology and oxidative stress

Theoretical analysis of biochemical pathways of nitric oxide release from vascular endothelial cells

Chen, Kejing, Popel, Aleksander S.·2006·Free Radical Biology and Medicine

Abstract

Vascular endothelium expressing endothelial nitric oxide synthase (eNOS) produces nitric oxide (NO), which has a number of important physiological functions in the microvasculature. The rate of NO production by the endothelium is a critical determinant of NO distribution in the vascular wall. We have analyzed the biochemical pathways of NO synthesis and formulated a model to estimate NO production by the microvascular endothelium under physiological conditions. The model quantifies the NO produced by eNOS based on the kinetics of NO synthesis and the availability of eNOS and its intracellular substrates. The predicted NO production from microvessels was in the range of 0.005-0.1 microM/s. This range of predicted values is in agreement with some experimental values but is much lower than other rates previously measured or estimated from experimental data with the help of mathematical modeling. Paradoxical discrepancies between the model predictions and previously reported results based on experimental measurements of NO concentration in the vicinity of the arteriolar wall suggest that NO can also be released through eNOS-independent mechanisms, such as catalysis by neuronal NOS (nNOS). We also used our model to test the sensitivity of NO production to substrate availability, eNOS concentration, and potential rate-limiting factors. The results indicated that the predicted low level of NO production can be attributed primarily to a low expression of eNOS in the microvascular end…

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Crossref · 10.1016/j.freeradbiomed.2006.05.009

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  • Reports for the maximum rate of NO production by NOS vary from 1 nM/s to 70 μM/s.

    “Unfortunately, the reports for the maximum rate of NO production by NOS vary from 1 nM/s to 70 μM/s [39–41].”

    From Mechanisms of nitrite bioactivation (2014) · cites this paper as [41]

  • With a concentration of 0.05 μM eNOS in an arteriole, the rate of nitrite reduction to NO by eNOS in anoxia would be 0.18 nM/sec.

    “With a concentration of 0.05 μM in an arteriole [41], the rate of nitrite reduction to NO by eNOS in anoxia would be 0.18 nM/sec.”

    From Mechanisms of nitrite bioactivation (2014) · cites this paper as [41]

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References 67 · Cited by 82

Authors
Chen, K., & Popel, A. S.
Affiliations
Johns Hopkins University (US)
Corresponding author
Chen, Kejing
Venue
Free Radical Biology and Medicine
Publisher
Elsevier BV
Published
2006-08
Volume
41
Issue
4
Pages
668-680
ISSN
0891-5849 (ISSN-L)
OpenAlex
W2030903898
Cited by
82
References
67
Citations by year
2025: 3 · 2024: 1 · 2023: 1 · 2022: 3 · 2021: 1 · 2020: 6 · 2019: 2 · 2018: 1 · 2017: 8 · 2016: 4 · 2015: 5 · 2014: 2 · 2013: 5 · 2012: 6
FWCI
3.53
Type
journal article
Language
en
Open access
closed
Locations
  • Free Radical Biology and Medicine (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institutes of Health (HL 18292, HL 79087)
Topics
  • Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Health and Disease Prevention
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
Keywords
nitric oxide, endothelial nitric oxide synthase, vascular endothelium, microvascular endothelial cells, neuronal nitric oxide synthase, substrate availability, rate-limiting factor
MeSH terms
Endothelium, Vascular, Humans, Nitric Oxide, Substrate Specificity, Nitric Oxide Synthase Type I, Nitric Oxide Synthase Type III

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