The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.
On the mechanism by which vascular endothelial cells regulate their oxygen consumption
Open accessAbstract
Two enzymes, soluble guanylyl cyclase and cytochrome c oxidase, have been shown to be exquisitely sensitive to nitric oxide (NO) at low physiological concentrations. Activation of the soluble guanylyl cyclase by endogenous NO and the consequent increase in the second messenger cyclic GMP are now known to control a variety of biological functions. Cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, is inhibited by NO. However, it is not clear whether NO produced by the constitutive NO synthase interacts with cytochrome c oxidase, nor is it known what the biological consequences of such an interaction might be. We now show that NO generated by vascular endothelial cells under basal and stimulated conditions modulates the respiration of these cells in response to acute changes in oxygen concentration. This action occurs at the cytochrome c oxidase and depends on influx of calcium. Thus, NO plays a physiological role in adjusting the capacity of this enzyme to use oxygen, allowing endothelial cells to adapt to acute changes in their environment.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Rotenone or amobarbital (a reversible inhibitor of complex I) given just before the onset of cardiac ischemia resulted in improved oxidative phosphorylation and retention of cytochrome c in mitochondria isolated during ischemia or on reperfusion (82, 85).”
From Mitochondrial reactive oxygen species production in excitable cells: Modulators of mitochondrial and cell function (2009) · cites this paper as [85]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor
Palmer, R. M. J., Ferrige, A. G., & Moncada, S. (1987) · Nature · doi:10.1038/327524a0 · Cited by 10,704
Self-citationCleeter, M. W. J., Cooper, J. M., Darley-Usmar, V. M., Moncada, S., & Schapira, A. H. V. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)00424-2 · Cited by 1,241
Self-citationOxygen sensing and molecular adaptation to hypoxia
Bunn, H. F., & Poyton, R. Ο. (1996) · Physiological Reviews · doi:10.1152/physrev.1996.76.3.839 · Cited by 1,185
Brown, G. C., & Cooper, C. E. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)01290-3 · Cited by 1,055
Self-citationClementi, E., Brown, G. C., Feelisch, M., & Moncada, S. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.13.7631 · Cited by 863
Self-citationMethods in Nitric Oxide Research
Young, J. (1997) · Physiological Measurement · doi:10.1088/0967-3334/18/1/008 · Cited by 749
Mitochondrial calcium transport: physiological and pathological relevance
Gunter, T. E., Gunter, K. K., Sheu, S. S., & Gavin, C. E. (1994) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1994.267.2.c313 · Cited by 698
García‐Cardeña, G., Oh, P., Liu, J., Schnitzer, J. E., & Sessa, W. C. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.13.6448 · Cited by 679
Production of Nitric Oxide by Mitochondria
Giulivi, C., Poderoso, J. J., & Boveris, A. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.18.11038 · Cited by 572
Nitric oxide synthase activity in mitochondria
Ghafourifar, P., & Richter, C. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)01397-5 · Cited by 567
Nitric oxide regulates mitochondrial respiration and cell functions by inhibiting cytochrome oxidase
Brown, G. C. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)00763-y · Cited by 540
Self-citationBolaños, J. P., Almeida, Á., Stewart, V. C., Peuchen, S., Land, J. M., Clark, J. B., & Heales, S. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.68062227.x · Cited by 519
Nitric Oxide Potently and Reversibly Deenergizes Mitochondria at Low Oxygen Tension
Schweizer, M., & Richter, C. (1994) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1994.2441 · Cited by 331
Role of nitric oxide in the regulation of oxygen consumption in conscious dogs.
Shen, W., Xu, X., Ochoa, M., Zhao, G., Wolin, M. S., & Hintze, T. H. (1994) · Circulation Research · doi:10.1161/01.res.75.6.1086 · Cited by 317
Control of mitochondrial and cellular respiration by oxygen
Gnaiger, E., Steinlechner-Maran, R., Méndez, G., Eberl, T., & Margreiter, R. (1995) · Journal of Bioenergetics and Biomembranes · doi:10.1007/bf02111656 · Cited by 316
Intracellular diffusion gradients of O2 and ATP
Jones, D. P. (1986) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1986.250.5.c663 · Cited by 268
Shen, W., Hintze, T. H., & Wolin, M. S. (1995) · Circulation · doi:10.1161/01.cir.92.12.3505 · Cited by 264
Xie, Y.-W., Shen, W., Zhao, G., Xu, X., Wolin, M. S., & Hintze, T. H. (1996) · Circulation Research · doi:10.1161/01.res.79.3.381 · Cited by 229
Gryglewski, R. J., Moncada, S., & Palmer, R. M. J. (1997) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1997.tb06839.x · Cited by 226
Self-citationMills, E., & Jöbsis, F. F. (1972) · Journal of Neurophysiology · doi:10.1152/jn.1972.35.4.405 · Cited by 221
Functional implications of nitric oxide produced by mitochondria in mitochondrial metabolism
Giulivi, C. (1998) · Biochemical Journal · doi:10.1042/bj3320673 · Cited by 213
Mitochondrial function in type I cells isolated from rabbit arterial chemoreceptors.
Duchen, M. R., & Biscoe, T. J. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp019114 · Cited by 207
Gryglewski, R. J., Moncada, S., & Palmer, R. M. J. (1986) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1986.tb14586.x · Cited by 200
Self-citationNitric oxide regulates oxygen uptake and hydrogen peroxide release by the isolated beating rat heart
Poderoso, J. J., Peralta, J. G., Lisdero, C. L., Carreras, M. C., Radisic, M., Schopfer, F. J., Cadenas, E., & Boveris, A. (1998) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1998.274.1.c112 · Cited by 194
A Role for Calcium Influx in the Regulation of Mitochondrial Calcium in Endothelial Cells
Lawrie, A. M., Rizzuto, R., Pozzan, T., & Simpson, A. W. M. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.18.10753 · Cited by 184
Clementi, E., Scheer, H., Zacchetti, D., Fasolato, C., Pozzan, T., & Meldolesi, J. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)45858-9 · Cited by 169
Self-citation[20] Regulation of mitochondrial respiration by adenosine diphosphate, oxygen, and nitric oxide
Boveris, A., Costa, L. E., Cadenas, E., & Poderoso, J. J. (1999) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(99)01082-4 · Cited by 137
Nitric oxide production in human endothelial cells stimulated by histamine requires Ca2+ influx
Lantoine, F., Iouzalen, L., Devynck, M., Brussel, E. M., & David‐Dufilho, M. (1998) · Biochemical Journal · doi:10.1042/bj3300695 · Cited by 124
Wilson, D. F., Mokashi, A., Chugh, D. K., Vinogradov, S. A., Osanai, S., & Lahiri, S. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)00887-6 · Cited by 122
López-Jaramillo, P. A., Gonzalez, M. C., Palmer, R. M. J., & Moncada, S. (1990) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1990.tb12735.x · Cited by 120
Self-citationTamura, M., Hazeki, O., Nioka, S., & Chance, B. (1989) · Annual Review of Physiology · doi:10.1146/annurev.ph.51.030189.004121 · Cited by 111
Cornfield, D. N., Stevens, T., McMurtry, I. F., Abman, S. H., & Rodman, D. M. (1994) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.1994.266.4.l469 · Cited by 103
Wang, Y., Shin, W. S., Kawaguchi, H., Inukai, M., Kato, M., Sakamoto, A., Uehara, Y., Miyamoto, M., Shimamoto, N., Korenaga, R., et al. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.10.5647 · Cited by 99
Oxygen dependence of mitochondrial function in isolated rat cardiac myocytes
Kennedy, F. G., & Jones, D. P. (1986) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1986.250.3.c374 · Cited by 97
Cellular energy utilization and supply during hypoxia in embryonic cardiac myocytes
Budinger, G. R. S., Chandel, N. S., Shao, Z. H., Li, C. Q., Melmed, A., Becker, L., & Schumacker, P. T. (1996) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.1996.270.1.l44 · Cited by 78
Xu, X. P., Pollock, J. S., Tanner, M. A., & Myers, P. R. (1995) · Cardiovascular Research · doi:10.1016/s0008-6363(95)00117-4 · Cited by 76
Regulation of Ca(2+)-dependent nitric oxide synthase in bovine aortic endothelial cells
Buckley, B. J., Mirza, Z., & Whorton, A. R. (1995) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1995.269.3.c757 · Cited by 62
In vivo comparison of cytochrome aa3 redox state and tissue PO2 in transient anoxia
Kariman, K., Hempel, F. G., & Jöbsis, F. F. (1983) · Journal of Applied Physiology · doi:10.1152/jappl.1983.55.4.1057 · Cited by 31
Research works printed but not linked: 3
- D N Cornfield, T Stevens, I F McMurtry, S H Abman, D M Rodman Am J Physiol 266, L469–L475 (1994).
- Boveris A. Costa L. Cadenas E. & Poderoso J. J. (1999) Methods. Enzymol. in press.
- G R Budinger, N Chandel, Z H Sha, C Q Li, A Melmed, L B Becker, P T Schumacker Am J Physiol 270, L44–L53 (1996).
Cited by
Sorted by citations
Oxidative Phosphorylation as an Emerging Target in Cancer Therapy
Ashton, T. M., McKenna, W. G., Kunz‐Schughart, L. A., & Higgins, G. S. (2018) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-17-3070 · Cited by 1,177
Physiology of Nitric Oxide in Skeletal Muscle
Stamler, J. S., & Meissner, G. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.1.209 · Cited by 1,080
Butow, R. A., & Avadhani, N. G. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00179-0 · Cited by 882
Does nitric oxide modulate mitochondrial energy generation and apoptosis?
Moncada, S., & Erusalimsky, J. D. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm762 · Cited by 794
Self-citationCooper, C. E., & Brown, G. C. (2008) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-008-9166-6 · Cited by 746
Self-citation
Metadata
- Authors
- Clementi, E., Brown, G. C., Foxwell, N., & Moncada, S.
- Affiliations
- University College London (GB)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1999-02-16
- Volume
- 96
- Issue
- 4
- Pages
- 1559-1562
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC15516
- OpenAlex
- W2067637944
- Cited by
- 296
- References
- 38
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 5 · 2023: 1 · 2022: 3 · 2021: 5 · 2020: 4 · 2019: 2 · 2018: 4 · 2017: 5 · 2016: 8 · 2015: 9 · 2014: 8 · 2013: 11 · 2012: 7
- FWCI
- 14.54
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) (submittedVersion, other-oa)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Wellcome Trust
- Consiglio Nazionale delle Ricerche
- Directorate for Biological Sciences
- Biotechnology and Biological Sciences Research Council
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Keywords
- nitric oxide, vascular endothelial cells, oxygen consumption, cytochrome c oxidase, soluble guanylate cyclase, cyclic GMP, nitric oxide synthase, mitochondrial respiration, calcium influx, oxygen sensing
- MeSH terms
- Animals, Aorta, Thoracic, Bradykinin, Calcium, Cells, Cultured, Egtazic Acid, Endothelium, Vascular, Nitric Oxide, Oxygen Consumption, Swine, omega-N-Methylarginine, NG-Nitroarginine Methyl Ester
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review