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Oxidation of the zinc-thiolate complex and uncoupling of endothelial nitric oxide synthase by peroxynitrite
Open accessAbstract
Nitric oxide (NO) is produced by NO synthase (NOS) in many cells and plays important roles in the neuronal, muscular, cardiovascular, and immune systems.In various disease conditions, all three types of NOS (neuronal, inducible, and endothelial) are reported to generate oxidants through unknown mechanisms.We present here the first evidence that peroxynitrite (ONOO -) releases zinc from the zinc-thiolate cluster of endothelial NOS (eNOS) and presumably forms disulfide bonds between the monomers.As a result, disruption of the otherwise SDS-resistant eNOS dimers occurs under reducing conditions.eNOS catalytic activity is exquisitely sensitive to ONOO -, which decreases NO synthesis and increases superoxide anion (O 2 .-)production by the enzyme.The reducing cofactor tetrahydrobiopterin is not oxidized, nor does it prevent oxidation of eNOS by the same low concentrations of OONO -.Furthermore, eNOS derived from endothelial cells exposed to elevated glucose produces more O 2 .-,and, like eNOS purified from diabetic LDL receptor-deficient mice, contains less zinc and fewer SDS-resistant dimers.Hence, eNOS exposure to oxidants including ONOO -causes increased enzymatic uncoupling and generation of O 2 .-indiabetes, contributing further to endothelial cell oxidant stress.Regulation of the zinc-thiolate center of NOS by ONOO -provides a novel mechanism for modulation of the enzyme function in disease.
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“Mitochondrial hydrogen peroxide can oxidize the catalytic subunit of AMP kinase, leading to its autophosphorylation and subsequent activation to modulate metabolism within the cell (481, 1067).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [1067]
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Cites
Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly
Beckman, J. S., & Koppenol, W. H. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.271.5.c1424 · Cited by 5,513
Regulation of biosynthesis of nitric oxide.
Nathan, C., & Xie, Q. W. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)36703-0 · Cited by 1,669
Superoxide generation by endothelial nitric oxide synthase: The influence of cofactors
Vásquez-Vivar, J., Kalyanaraman, B., Martásek, P., Hogg, N., Masters, B. S. S., Karoui, H., Tordo, P., & Pritchard, K. A. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.16.9220 · Cited by 1,484
Nitric oxide synthase structure and mechanism
Marletta, M. A. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)31375-9 · Cited by 1,338
Mechanisms Underlying Endothelial Dysfunction in Diabetes Mellitus
Hink, U., Li, H., Mollnau, H., Oelze, M., Matheis, E., Hartmann, M., Skatchkov, M. P., Thaiss, F., Stahl, R. A. K., Warnholtz, A., et al. (2001) · Circulation Research · doi:10.1161/01.res.88.2.e14 · Cited by 1,191
Nitric oxide synthases: which, where, how, and why?
Michel, T. M., & Féron, O. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119750 · Cited by 1,024
Oxidative Damage and Tyrosine Nitration from Peroxynitrite
Beckman, J. S. (1996) · Chemical Research in Toxicology · doi:10.1021/tx9501445 · Cited by 993
Pollock, J. S., Förstermann, U., Mitchell, J. A., Warner, T. D., Schmidt, H. H. H. W., Nakane, M., & Murad, F. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.23.10480 · Cited by 979
Activation of molecular oxygen by flavins and flavoproteins.
Massey, V. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)31664-2 · Cited by 823
Cosentino, F., Hishikawa, K., Katušić, Z. S., & Lüscher, T. F. (1997) · Circulation · doi:10.1161/01.cir.96.1.25 · Cited by 762
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Items 401–494 of 494
Is tetrahydrobiopterin a therapeutic option in diabetic hypertensive patients?
Rubio-Guerra, A. F. (2010) · Integrated Blood Pressure Control · doi:10.2147/ibpc.s7479 · Cited by 15
Oates, J. C., Farrelly, L. W., Hofbauer, A. F., Wang, W., & Gilkeson, G. S. (2007) · Arthritis & Rheumatism · doi:10.1002/art.22955 · Cited by 14
Nikrad, N., Shakarami, A., Tousi, A. Z., Farhangi, M. A., Ardekani, A. M., & Jafarzadeh, F. (2023) · BMC Endocrine Disorders · doi:10.1186/s12902-023-01392-5 · Cited by 13
Spotlight on endothelial progenitor cell inhibitors: short review
Thum, T., & Bauersachs, J. K. (2005) · Vascular Medicine · doi:10.1177/1358836x0501000109 · Cited by 13
Tinahones, F. J., Cardona, F., Rojo‐Martínez, G., Almaraz, M. C., Cardona, I., Vázquez‐Mellado, J., Garrido‐Sánchez, L., Collantes‐Estévez, E., & Soriguer, F. (2007) · British Journal Of Nutrition · doi:10.1017/s0007114507787470 · Cited by 13
Nutraceutical Prevention of Diabetic Complications—Focus on Dicarbonyl and Oxidative Stress
McCarty, M. F., DiNicolantonio, J. J., & O’Keefe, J. H. (2022) · Current Issues in Molecular Biology · doi:10.3390/cimb44090297 · Cited by 13
Gao, S.-Q., Shi, J., Xue-Wang, Miao, S.-H., Li, T., Gao, C.-C., Han, Y., Qiu, J.-Y., Zhuang, Y.-S., & Zhou, M. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.10.318 · Cited by 12
Vorotnikov, A. V., Khapchaev, A. Y., Nickashin, A. V., & Shirinsky, V. P. (2022) · Biomedicines · doi:10.3390/biomedicines10123181 · Cited by 13
Additive renoprotective effect of candesartan and tetrahydrobiopterin in rats after 5/6 nephrectomy
Podjarny, E., Bernheim, J., Hasdan, G., Karsh, D. E., Rashid, G., Green, J., Katz, B., & Bernheim, J. (2007) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfm129 · Cited by 12
Oxidative Inactivation of Nitric Oxide and Peroxynitrite Formation in the Vasculature
Subelzú, N., Bartesaghi, S., Bem, A. F. D., & Radí, R. (2015) · ACS symposium series · doi:10.1021/bk-2015-1200.ch004 · Cited by 12
Sato, A., Yumita, Y., Kagami, K., Ishinoda, Y., Kimura, T., Osaki, A., Toya, T., Namba, T., Endo, S., Ido, Y., et al. (2022) · Journal of the American Heart Association · doi:10.1161/jaha.122.027538 · Cited by 11
Chemoproteomic Profiling Maps Zinc-Dependent Cysteine Reactivity
Qiu, N., Pechalrieu, D., Abegg, D., & Adibekian, A. (2024) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.3c00416 · Cited by 10
Mitophagy: A Potential Target for Pressure Overload‐Induced Cardiac Remodelling
Shao, R., Li, J., Qu, T., Liao, Y., & Chen, M. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/2849985 · Cited by 11
Jelinic, M., Leo, C. H., Marshall, S. A., Senadheera, S. N., Parry, L. J., & Tare, M. (2017) · Microcirculation · doi:10.1111/micc.12371 · Cited by 11
CaMKII in Vascular Signalling: “Friend or Foe”?
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Future outlook for drug eluting stents
Vedantham, K., Chaterji, S., Kitsongsermthon, J., Park, K., & GARNER, J. (2010) · Elsevier eBooks · doi:10.1533/9781845697488.2.118 · Cited by 11
Pereira, A., Olivon, V. C., & de Oliveira, A. M. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.05.051 · Cited by 11
Münzel, T. F., & Daiber, A. (2018) · Cardiovascular Research · doi:10.1093/cvr/cvy118 · Cited by 11
Hasan Anıl, K. U. R. T., Demirci, E., & Alan, C. (2022) · Disease Markers · doi:10.1155/2022/3661822 · Cited by 10
Peroxynitrite Formation and Detection in Living Cells
Ríos, N., Prolo, C., Álvarez, M. N., Piacenza, L., & Radí, R. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804273-1.00021-1 · Cited by 10
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Alban, F. T. E., Gyamfi, D., van Golen, R. F., & Heger, M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-803951-9.00008-2 · Cited by 11
Diabetes mellitus, oxidative stress and endothelial dysfunction
Sydow, K., & Münzel, T. F. (2003) · International Congress Series · doi:10.1016/s0531-5131(02)01280-3 · Cited by 11
Slyvka, Y., Wang, Z., Yee, J., Inman, S. R., & Nowak, F. V. (2010) · Nitric Oxide · doi:10.1016/j.niox.2010.11.004 · Cited by 10
Hekimoğlu, A., Bilgin, H. M., Kurçer, Z., & Ocak, A. R. (2009) · Archives of Gynecology and Obstetrics · doi:10.1007/s00404-009-1044-x · Cited by 9
Gonzalez-Vazquez, A., Aguilar-Peralta, A. K., Tomás-Sanchez, C., Blanco-Álvarez, V. M., Martínez‐Fong, D., González-Barrios, J. A., Treviño, S., Peña, L. M.-P., Alatriste, V., Soto-Rodríguez, G., et al. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/6696538 · Cited by 9
Suvorava, T., Pick, S., & Kojda, G. (2016) · Journal of Hypertension · doi:10.1097/hjh.0000000000001127 · Cited by 9
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Palm, F., Nordquist, L., Wilcox, C. S., & Hansell, P. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-857-7_29 · Cited by 9
Horn, A. G., White, Z. J., Hall, S. E., Morrison, K. J., Schulze, K. M., Muller‐Delp, J. M., Poole, D. C., & Behnke, B. J. (2025) · The Journal of Physiology · doi:10.1113/jp287451 · Cited by 8
Effect of secondary hyperparathyroidism serum on endothelial cells and intervention with Klotho
Chen, C., Mao, H., Yu, X., Sun, B., ZENG, M., Zhao, X., Qian, J., Liu, J., & Xing, C. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.3606 · Cited by 8
Liu, J., Huang, Z., Ma, W., Peng, S., Li, Y., Miranda, K. M., Tian, J., & Zhang, Y. (2018) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2018.10.006 · Cited by 8
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Fleming, I. (2008) · Comprehensive physiology · doi:10.1002/cphy.cp020403 · Cited by 7
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Sun, X., Caceres, S. M., Yegambaram, M., Lü, Q., Pokharel, M. D., Boehme, J. B., Datar, S. A., Aggarwal, S., Wang, T., Fineman, J. R., et al. (2024) · Nitric Oxide · doi:10.1016/j.niox.2024.09.009 · Cited by 7
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Kuo, L., Thengchaisri, N., & Hein, T. W. (2012) · Molecular Medicine & Therapeutics · doi:10.4172/2324-8769.1000101 · Cited by 7
Nitrosation of N‐Terminally Blocked Tryptophan and Tryptophan‐Containing Peptides by Peroxynitrite
Peyrot, F., & Ducrocq, C. (2006) · ChemBioChem · doi:10.1002/cbic.200600385 · Cited by 7
Wang, X., Zeng, C., Gong, H., He, H., Wang, M., Hu, Q., & Yang, F. (2014) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmu073 · Cited by 7
Lee, J. W., Ovadia, B., Azakie, A., Salas, S., Goerke, J., Fineman, J. R., & Gutierrez, J. A. (2004) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00271.2003 · Cited by 7
Les espèces réactives de l’azote : bénéfiques ou délétères ?
Massion, P. B., Preiser, J., & Balligand, J. (2002) · Nutrition Clinique et Métabolisme · doi:10.1016/s0985-0562(02)00167-x · Cited by 7
End-organ susceptibility as a determinant of renal disease in hypertension
Raij, L. R. (2003) · Kidney International · doi:10.1046/j.1523-1755.2003.00291.x · Cited by 7
Ogata, M., & YAMAZAKI, Y. (1979) · PubMed · doi:10.18926/amo/32049 · Cited by 7
Thromboxane-dependent coronary vasoconstriction in obese mice: Role of peroxynitrite
Villa, E., López-Vaquera, S. R., Alvarado-Coutiño, L. K., Gámez-Méndez, A. M., Rı́os, A., & Escalante, B. (2022) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2022.106631 · Cited by 6
Acetylcholine acutely modifies nitric oxide synthase function in the human coronary circulation
Miner, S. E. S., Al‐Hesayen, A., Nield, L. E., Gori, T., & Parker, J. D. (2010) · Experimental Physiology · doi:10.1113/expphysiol.2010.053926 · Cited by 6
Münzel, T. F., & Daiber, A. (2017) · British Journal of Pharmacology · doi:10.1111/bph.13827 · Cited by 5
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Rafikov, R., Kumar, S., Aggarwal, S., Pardo, D., Fonseca, F. V., Ransom, J., Rafikova, O., Chen, Q., Springer, M. L., & Black, S. M. (2014) · Redox Biology · doi:10.1016/j.redox.2013.12.015 · Cited by 5
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Signorello, M. G., & Leoncini, G. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26041421 · Cited by 4
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Barbeiro, H. V., Barbeiro, D. F., Debbas, V., de Souza, H. P., Laurindo, F. R. M., Velasco, I. T., & Soriano, F. G. (2009) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x2009005000029 · Cited by 4
Xie, L., Hu, D., Qin, H., Zhang, W., Zhang, S., Feng, Y., Yao, H., Xiao, Y., Yao, K., & Huang, X. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.01.026 · Cited by 4
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Schulz, E., & Keaney, J. F. (2003) · Current Opinion in Endocrinology & Diabetes · doi:10.1097/00060793-200308000-00002 · Cited by 4
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Wihastuti, T. A., Sargowo, D., Soeharto, S., Heriansyah, T., & Widyasih, G. R. (2015) · Journal of Medical and Bioengineering · doi:10.12720/jomb.4.5.342-349 · Cited by 3
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Li, M., Shen, A., Gao, X., Lin, C., Huang, Z., Lv, Q., Tang, J., Ma, X., Ni, J., Tian, J., et al. (2025) · Advanced Science · doi:10.1002/advs.202510298 · Cited by 2
Zou, M., & Wu, S. (2021) · Cardiology Discovery · doi:10.1097/cd9.0000000000000009 · Cited by 2
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Camp, O. G., Goud, A. P., Goud, P. T., Bai, D., Awonuga, A. O., & Abu‐Soud, H. M. (2023) · F&S Science · doi:10.1016/j.xfss.2023.02.002 · Cited by 2
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(2005) · CRC Press eBooks · doi:10.1201/9781420030853.pt3 · Cited by 1
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Ahmed, I. O., & Ogunlade, O. (2022) · Research Square · doi:10.21203/rs.3.rs-2316306/v1 · Cited by 1
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Ng, D. S. (2006) · Wiley-VCH eBooks · doi:10.1002/3527600906.mcb.200400011
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VanGilder, R. L. (2009) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.4544
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Marvar, P. J. (2006) · doi:10.33915/etd.4246
Li, Z., Zhang, L., Zhou, L., Li, X., Zhao, Y., & Wang, J. (2023) · Biosurface and Biotribology · doi:10.1049/bsb2.12060
Mekrungruangwong, T., Patumraj, S., & Viboolvorakul, S. (2019) · doi:10.58837/chula.the.2019.368
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Biology of Nitric Oxide Synthases
Fleming, I. (1984) · Comprehensive physiology · doi:10.1002/j.2040-4603.1984.tb01012.x
Bahadoran, Z., Hosseinpanah, F., Dehghan, P., & Azizi, F. (2026) · Cardiovascular Toxicology · doi:10.1007/s12012-026-10146-3
Metadata
- Authors
- Zou, M.-H., Shi, C., & Cohen, R. A.
- Affiliations
- Boston University (US)
- Corresponding author
- Zou, Ming-Hui
- Venue
- Journal of Clinical Investigation
- Published
- 2002-03-15
- Volume
- 109
- Issue
- 6
- Pages
- 817-826
- ISSN
- 0021-9738 (ISSN-L)
- OpenAlex
- W4254181710
- Cited by
- 494
- References
- 48
- Citations by year
- 2026: 1 · 2025: 10 · 2024: 7 · 2023: 12 · 2022: 19 · 2021: 12 · 2020: 17 · 2019: 15 · 2018: 19 · 2017: 23 · 2016: 15 · 2015: 22 · 2014: 22 · 2013: 22 · 2012: 29
- FWCI
- 17.56
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Investigation (publishedVersion)
- Funders
- American Heart Association
- National Institutes of Health (PO1 HL)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Keywords
- peroxynitrite, endothelial nitric oxide synthase, superoxide production, tetrahydrobiopterin, disulfide bonds, oxidative stress, diabetes mellitus, endothelial cells, nitric oxide production
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 ›
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