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Circulating plasma xanthine oxidase contributes to vascular dysfunction in hypercholesterolemic rabbits.
Open accessAbstract
Reactive oxygen species play a central role in vascular inflammation and atherogenesis, with enhanced superoxide (O2.-) production contributing significantly to impairment of nitric oxide (.NO)-dependent relaxation of vessels from cholesterol-fed rabbits. We investigated potential sources of O2.- production, which contribute to this loss of endothelium-dependent vascular responses. The vasorelaxation elicited by acetylcholine (ACh) in phenylephrine-contracted, aortic ring segments was impaired by cholesterol feeding. Pretreatment of aortic vessels with either heparin, which competes with xanthine oxidase (XO) for binding to sulfated glycosaminoglycans, or the XO inhibitor allopurinol resulted in a partial restoration (36-40% at 1 muM ACh) of ACh-dependent relaxation. Furthermore, O2.(-)-dependent lucigenin chemiluminescence, measured in intact ring segments from hypercholesterolemic rabbits, was decreased by addition of heparin, allopurinol or a chimeric, heparin-binding superoxide dismutase. XO activity was elevated more than two-fold in plasma of hypercholesterolemic rabbits. Incubation of vascular rings from rabbits on a normal diet with purified XO (10 milliunits/ml) also impaired .NO-dependent relaxation but only in the presence of purine substrate. As with vessels from hypercholesterolemic rabbits, this effect was prevented by heparin and allopurinol treatment. We hypothesize that increases in plasma cholesterol induce the release of XO into the circulation, where it binds to endothelial cell glycosaminoglycans. Only in hypercholesterolemic vessels is sufficient substrate available to sustain the production of O2.- and impair NO-dependent vasorelaxation. Chronically, the continued production of peroxynitrite, (ONOO-) which the simultaneous generation of NO and O2.- implies, may irreversibly impair vessel function.
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“In addition, BH4 plays a critical role in the catalytic cycle of NOS (87, 204, 377, 904, 933, 1000, 1007).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [1007]
In the citing paper
“Thus, not only is the NO synthesis completely abolished but the protein also becomes an oxidase, generating superoxide instead of NO (191, 972, 1007) (Table 6).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [1007]
In the citing paper
“Mechanistically, when NOS binds BH2 instead of BH4, the ferrous/oxy heme cannot hydroxylate l-arginine to NG-hydroxy-l-arginine, NO synthesis is blocked, and the oxygen is eventually oxidized to superoxide.”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [1007]
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Cites
PROTEOGLYCANS: STRUCTURES AND INTERACTIONS
Kjellén, L., & Lindahl, U. (1991) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.60.070191.002303 · Cited by 1,900
Hypercholesterolemia increases endothelial superoxide anion production.
Ohara, Y., Peterson, T. E., & Harrison, D. G. (1993) · Journal of Clinical Investigation · doi:10.1172/jci116491 · Cited by 1,765
Proteoglycans: Structures And Interactions
Kjellén, L. (1991) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.60.1.443 · Cited by 1,602
Extensive Nitration of Protein Tyrosines in Human Atherosclerosis Detected by Immunohistochemistry
Beckman, J. S., Ye, Y. Z., Anderson, P. G., Chen, J., Accavitti, M. A., Tarpey, M. M., & White, C. R. (1994) · Biological Chemistry Hoppe-Seyler · doi:10.1515/bchm3.1994.375.2.81 · Cited by 1,122
Self-citationDoes superoxide underlie the pathogenesis of hypertension?
Nakazono, K., Watanabe, N., Matsuno, K., Sasaki, J., Sato, T., & Inoue, M. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.22.10045 · Cited by 746
Superoxide and peroxynitrite inatherosclerosis.
White, C. R., Brock, T. A., Chang, L. Y., Crapo, J. D., BRISCOE, P. M., Ku, D. D., Bradley, W. A., Gianturco, S. H., Gore, J. Z., & Freeman, B. Α. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.3.1044 · Cited by 684
Self-citationMünzel, T. F., Sayegh, H. S., Freeman, B. Α., Tarpey, M. M., & Harrison, D. G. (1995) · Journal of Clinical Investigation · doi:10.1172/jci117637 · Cited by 652
Self-citationNitric oxide and oxygen radicals: a question of balance
Darley-Usmar, V. M., Wiseman, H., & Halliwell, B. B. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)00764-z · Cited by 557
Self-citationBossaller, C., Habib, G. B., Yamamoto, H., Williams, C., Wells, S., & Henry, P. D. (1987) · Journal of Clinical Investigation · doi:10.1172/jci112779 · Cited by 531
Pritchard, K. A., Groszek, L., Smalley, D. M., Sessa, W. C., Wu, M., Villalon, P., Wolin, M. S., & Stemerman, M. B. (1995) · Circulation Research · doi:10.1161/01.res.77.3.510 · Cited by 470
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Serum uric acid as a cardiovascular risk factor for heart disease
Alderman, M. H. (2001) · Current Hypertension Reports · doi:10.1007/s11906-001-0036-4 · Cited by 44
Atherosclerosis and the Hypercholesterolemic AGE–RAGE Axis
Qureshi, M., Prasad, K., Pearce, C., & McNair, E. (2016) · International Journal of Angiology · doi:10.1055/s-0035-1570754 · Cited by 44
Kurose, I., Wolf, R. E., Grisham, M. B., & Granger, D. N. (1998) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.18.10.1583 · Cited by 42
Reactive oxygen species and the control of vasomotor tone
Somers, M. J., & Harrison, D. G. (1999) · Current Hypertension Reports · doi:10.1007/s11906-999-0080-z · Cited by 41
Probucol Protects against Hypochlorite-induced Endothelial Dysfunction
Witting, P. K., Wu, B. J., Raftery, M. J., Southwell‐Keely, P. T., & Stocker, R. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m414256200 · Cited by 39
Restoring the Dysfunctional Endothelium
Osto, E., Coppolino, G., Volpe, M., & Cosentino, F. (2007) · Current Pharmaceutical Design · doi:10.2174/138161207780487566 · Cited by 39
Veerareddy, S., Cooke, C. M., Baker, P. N., & Davidge, S. T. (2004) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01179.2003 · Cited by 39
Go, Y., Levonen, A., Moellering, D. R., Ramachandran, A., Patel, R. P., Jo, H., & Darley-Usmar, V. M. (2001) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2001.281.6.h2705 · Cited by 39
Self-citationSerum Xanthine Oxidase: Origin, Regulation, and Contribution to Control of Trypanosome Parasitemia
Wang, J., Praagh, A. D. G. V., Hamilton, E., Wang, Q. L., Zou, B.-X., Muranjan, M., Murphy, N. B., & Black, S. J. (2002) · Antioxidants and Redox Signaling · doi:10.1089/152308602753625933 · Cited by 39
Whitsett, J., Pavel Martasek, E., Zhao, H., Schauer, D. W., Hatakeyama, K., Kalyanaraman, B., & Vasquez-Vivar, J. M. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2006.02.001 · Cited by 39
Peri/Epicellular Thiol Oxidoreductases as Mediators of Extracellular Redox Signaling
Tanaka, L. Y., Oliveira, P., & Laurindo, F. R. M. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2019.8012 · Cited by 37
Is ceruloplasmin an important catalyst for S-nitrosothiol generation in hypercholesterolemia?
Moriel, P., Pereira, I. R. O., Bertolami, M. C., & Abdalla, D. S. P. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00467-6 · Cited by 37
Diet and Atherosclerosis in Apolipoprotein E-Deficient Mice
Imaizumi, K. (2011) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.110059 · Cited by 35
Martínez‐Hervás, S., Real, J. T., Ivorra, C., Priego, A., Chaves, F. J., Pallardó, F. V., Vinã, J. R., Redón, J., Carmena, R., & Ascaso, J. F. (2009) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2009.06.003 · Cited by 35
Sega, F. V. D., Aquila, G., Fortini, F., Vaccarezza, M., Secchiero, P., Rizzo, P., & Campo, G. C. (2017) · BioFactors · doi:10.1002/biof.1359 · Cited by 35
UNRAVELING PEROXYNITRITE FORMATION IN BIOLOGICAL SYSTEMS
Radí, R., Peluffo, G., ALVAREZ, M. N., Naviliat, M., & Cayota, A. (2001) · Elsevier eBooks · doi:10.1016/b978-0-444-50957-4.50038-7 · Cited by 32
Oyagbemi, A. A., Azeez, O. I., & Saba, A. B. (2009) · PubMed · Cited by 34
A Computational Model for Free Radicals Transport in the Microcirculation
Kavdia, M. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2006.8.1103 · Cited by 33
Hayashi, T., Arockia, J. R. P., Fukatsu, A., Matsui‐Hirai, H., Osawa, M., Miyazaki, A., Tsunekawa, T., Kano-Hayashi, H., Iguchi, A., Sumi, D., et al. (2004) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2003.12.034 · Cited by 33
Oxidases and Oxygenases in Regulation of Vascular Nitric Oxide Signaling and Inflammatory Responses
Aslan, M., & Freeman, B. Α. (2002) · Immunologic Research · doi:10.1385/ir:26:1-3:107 · Cited by 32
Self-citationWhite, C. R., Moellering, D. R., Patel, R. P., KIRK, M. C., Barnes, S., & Darley-Usmar, V. M. (1997) · Biochemical Journal · doi:10.1042/bj3280517 · Cited by 32
Self-citationKhambata, R. S., Ghosh, S. M., & Ahluwalia, A. (2015) · Antioxidants and Redox Signaling · doi:10.1089/ars.2015.6254 · Cited by 30
Nitric Oxide and Low-Density Lipoprotein Oxidation
Hogg, N., & Kalyanaraman, B. (1998) · Free Radical Research · doi:10.3109/10715769809065815 · Cited by 30
Xanthine Oxidoreductase Function Contributes to Normal Wound Healing
Madigan, M. C., McEnaney, R. M., Shukla, A. J., Hong, G., Kelley, E. E., Tarpey, M. M., Gladwin, M. T., Zuckerbraun, B. S., & Tzeng, E. (2015) · Molecular Medicine · doi:10.2119/molmed.2014.00191 · Cited by 28
Self-citationRole of cholesterol-enriched diet and the mevalonate pathway in cardiac nitric oxide synthesis
Giricz, Z., Csonka, C., �nody, A., Csont, T., & Ferdinandy, P. (2003) · Basic Research in Cardiology · doi:10.1007/s00395-003-0412-0 · Cited by 29
Clark, S., Coffey, M. J., Maclean, R., Collins, P. W., LEWIS, M. J., Cross, A. R., & O’Donnell, V. B. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.10.5889 · Cited by 27
Falco, L., Tessitore, V., Ciccarelli, G., D’Aquino, M. M. C., D’Andrea, A., Imbalzano, E., Golino, P., & Russo, V. (2023) · Antioxidants · doi:10.3390/antiox12061185 · Cited by 29
Kelley, E. E. (2015) · Archives of Toxicology · doi:10.1007/s00204-015-1523-8 · Cited by 30
Heck, D. E. (2001) · Antioxidants and Redox Signaling · doi:10.1089/152308601300185205 · Cited by 26
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Foresman, E. L., & Miller, F. J. (2013) · Redox Biology · doi:10.1016/j.redox.2013.04.003 · Cited by 24
Li, H., Zhang, C., Zhang, H., & Li, H. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174270 · Cited by 24
Girault, I., Karu, A. E., Schaper, M., Barcellos‐Hoff, M. H., Hagen, T. M., Vogel, D. S., Ames, B. N., Christen, S., & Shigenaga, M. K. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00712-2 · Cited by 23
Pacheco, J. T., Daleprame, J. B., & Boaventura, G. T. (2011) · PubMed · doi:10.1590/s0212-16112011000400019 · Cited by 23
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Jeong, H. Y., Jeong, H. Y., & Kim, C. D. (2003) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2003.10.004 · Cited by 23
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Washio, K., Kusunoki, Y., Tsunoda, T., Osugi, K., Ohigashi, M., Murase, T., Nakamura, T., Matsuo, T., Konishi, K., Katsuno, T., et al. (2019) · Acta Diabetologica · doi:10.1007/s00592-019-01362-1 · Cited by 22
Yaghoubi, M., Oliver-Krasinski, J. M., Cayatte, A. J., & Cohen, R. A. (2000) · Journal of Cardiovascular Pharmacology · doi:10.1097/00005344-200012000-00010 · Cited by 22
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Bult, H., Matthys, K. E., & Kockx, M. M. (2000) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-57077-3_23 · Cited by 21
Nitric Oxide and Blood Pressure in Mice Lacking Extracellular-Superoxide Dismutase
Jönsson, L., Rees, D. D., Edlund, H., & Marklund, S. L. (2002) · Free Radical Research · doi:10.1080/10715760290032629 · Cited by 22
Minami, M., Ishiyama, A., Takagi, M., Omata, M., & Atarashi, K. (2005) · Blood Pressure · doi:10.1080/08037050510008878 · Cited by 21
Deckert, V., Duverneuil, L., Poupon, S., Monier, S., Guern, N. L., Lizard, G., Masson, D., & Lagrost, L. (2002) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0704920 · Cited by 21
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Mitani, H., Egashira, K., Ohashi, N., Yoshikawa, M., Niwa, S., Nonomura, K., Nakashima, A., & Kimura, M. (2003) · Pharmacology · doi:10.1159/000070169 · Cited by 19
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Dambrova, M., Uhlén, S., Welch, C. J., & Wikberg, J. E. S. (1998) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.1998.2570178.x · Cited by 18
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Ferraris, S., van der Merwe, J., der Veeken, L. V., Prados, F., Iglesias, J. E., Melbourne, A., Lorenzi, M., Marc Modat, A., Gsell, W., Deprest, J. A., et al. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.06.029 · Cited by 17
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Strålin, P., Jacobsson, H., & Marklund, S. L. (2002) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/s0304-4165(02)00419-1 · Cited by 18
Latourte, A., Bardin, T., Clerson, P., Ea, H., Flipo, R., & Richette, P. (2017) · Arthritis Care & Research · doi:10.1002/acr.23347 · Cited by 17
Simonet, S., Rupin, A., Badier‐Commander, C., Coumailleau, S., Behr‐Roussel, D., & Verbeuren, T. J. (2004) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2004.03.052 · Cited by 16
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da Luz, P. L., Chagas, A. C. P., Dourado, P. M. M., & Laurindo, F. R. M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812348-5.00033-7 · Cited by 16
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Webb, A., & Ahluwalia, A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-373866-0.00017-4 · Cited by 15
Ghouleh, I. A., & Magder, S. A. (2008) · Shock · doi:10.1097/shk.0b013e318157ebc8 · Cited by 15
Daghini, E., Chade, A., Krier, J. D., Versari, D., Lerman, A., & Lerman, L. O. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00436.2005 · Cited by 15
Schwemmer, M., Sommer, O., & Bassenge, E. (2000) · Cardiovascular Drugs and Therapy · doi:10.1023/a:1007838809551 · Cited by 15
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Multiple organ dysfunction syndrome: Role of xanthine oxidase and nitric oxide
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Self-citationLópez‐Cruz, R. I., Pérez-Milicua, M. B., Crocker, D. E., Gaxiola‐Robles, R., Bernal-Vertiz, J. A., de la Rosa, A., Vázquez‐Medina, J. P., & Zenteno‐Savín, T. (2014) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2014.02.007 · Cited by 12
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White, C. R., Parks, D. A., Patel, R. P., Shelton, J. E., Tarpey, M. M., Freeman, B. Α., & Darley-Usmar, V. M. (2004) · FEBS Letters · doi:10.1016/s0014-5793(04)00137-1 · Cited by 12
Self-citationYun, M. R., Im, D., Lee, J., Son, S. M., Sung, S., Bae, S. S., & Kim, C. D. (2005) · Life Sciences · doi:10.1016/j.lfs.2005.10.044 · Cited by 12
Yeh, G. C., Henderson, J. P., Byun, J., d’Avignon, D. A., & Heinecke, J. W. (2003) · Archives of Biochemistry and Biophysics · doi:10.1016/s0003-9861(03)00256-x · Cited by 12
Medina, J. S., Muñoz, M., Rodríguez, C., Contreras, C., Sánchez, A., Coronado, M. J., Ramil, E., Santos, M., Carballido, J., & Prieto, D. (2022) · Cells · doi:10.3390/cells11152306 · Cited by 11
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Jani, N. V., Ziogas, J., Angus, J. A., Schiesser, C. H., Macdougall, P. E., Grange, R. L., & Wright, C. E. (2012) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2012.08.003 · Cited by 10
Ashry, N. A., Abdelaziz, R. R., Suddek, G. M., & Saleh, M. A. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119731 · Cited by 10
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Zeng, C., Wang, X., Hu, X., Chen, J.-Z., & Wang, L. (2006) · Medical Hypotheses · doi:10.1016/j.mehy.2006.09.062 · Cited by 10
Vasilyeva, A. D., Yurina, L. V., Ivanov, V. S., Azarova, D. Y., Gavrilina, E. S., Indeykina, M. I., Bugrova, A. E., Kononikhin, A. S., Nikolaev, E., & Rosenfeld, M. A. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.02.128 · Cited by 9
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Metadata
- Authors
- White, C. R., Darley-Usmar, V, Berrington, W. R., McAdams, M., Gore, J. Z., Thompson, J. A., Parks, D. A., Tarpey, M. M., & Freeman, B. A.
- Affiliations
- University of Alabama at Birmingham (US)
- Department of Medicine, University of Alabama at Birmingham 35294, USA.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1996-08-06
- Volume
- 93
- Issue
- 16
- Pages
- 8745-8749
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC38744
- OpenAlex
- W2012018808
- Cited by
- 367
- References
- 39
- Citations by year
- 2026: 1 · 2025: 1 · 2023: 2 · 2022: 6 · 2021: 5 · 2020: 7 · 2019: 6 · 2018: 12 · 2017: 12 · 2016: 9 · 2015: 10 · 2014: 17 · 2013: 7 · 2012: 5
- FWCI
- 9.59
- 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)
- Funders
- American Heart Association
- National Institutes of Health (5k08hl003457-04, 5p01hl048676-05, 5r01hl051245-05)
- National Heart, Lung, and Blood Institute (P01 HL 48676, R01 HL 51245, KO8-HL03457)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Health Sciences › Medicine › Nephrology › Gout, Hyperuricemia, Uric Acid
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Keywords
- xanthine oxidase, hypercholesterolemia, reactive oxygen species, superoxide, endothelial dysfunction, allopurinol, heparin, glycosaminoglycans, peroxynitrite, atherosclerosis, acetylcholine, cholesterol-fed rabbits
- MeSH terms
- Acetylcholine, Animals, Endothelium, Vascular, Glycosaminoglycans, Hypercholesterolemia, Luminescent Measurements, Muscle, Smooth, Vascular, Nitric Oxide, Rabbits, Superoxides, Vasodilation, Xanthine Oxidase, In Vitro Techniques
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