Cited by 302Nitric Oxide and Endothelin EffectsNeutrophil, Myeloperoxidase and Oxidative MechanismsRedox biology and oxidative stress

The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.

An NADPH oxidase superoxide-generating system in the rabbit aorta

Pagano, P. J., Ito, Y., Tornheim, K., Gallop, P. M., Tauber, A. I., Cohen, R. A.·1995·American Journal of Physiology-Heart and Circulatory Physiology

DOI 10.1152/ajpheart.1995.268.6.h2274

Open this paper in CoChat — free account

Abstract

Superoxide anion can modulate vascular smooth muscle tone and potentially affect the growth response in vascular disease. The present studies were undertaken to characterize the source of superoxide in rabbit aorta. Rings of aorta (5 mm) were incubated in physiological salt solution (PSS) for 30 min at 37 degrees C in the presence of 10 mM diethyldithiocarbamate (DDC) with or without inhibitors of superoxide-generating systems. Rings were then placed in PSS containing 250 microM lucigenin at 37 degrees C in the presence or absence of inhibitors, and changes in amounts of superoxide were determined by measuring chemiluminescence (units). The inhibitors of xanthine oxidase, oxypurinol (300 microM), and of mitochondrial NADH dehydrogenase, rotenone (50 microM), had no significant effect on superoxide levels. An inhibitor of NADPH oxidase, iodonium thiophen, caused a concentration-dependent inhibition of superoxide anion (12.49 +/- 1.48 vs 5.27 +/- 1.81 and 2.30 +/- 0.36 units, control vs 7 microM and 70 microM iodonium thiopen, respectively). A structurally related iodonium compound, diphenyleneiodonium (20 microM), caused a 78% reduction in basal and DDC-evoked superoxide levels. In the presence or absence of DDC, exogenous administration of NADPH (10 microM-1 mM), but not NADP (1 mM), elicited a concentration-dependent rise in superoxide levels that was inhibited by iodonium thiophen. Particulate fractions of whole aortic tissue exhibited NADPH-dependent superoxide production that was inhibited by 1 microM diphenyleneiodonium.(ABSTRACT TRUNCATED AT 250 WORDS)

Integrity signals

Registry

Crossref · 10.1152/ajpheart.1995.268.6.h2274

Cites

24 of 24 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

Superoxide Dismutase
McCord, J. M., & Fridovich, I. (1969) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)63504-5 · Cited by 12,952
Superoxide anion is involved in the breakdown of endothelium-derived vascular relaxing factor
Gryglewski, R. J., Palmer, R. M. J., & Moncada, S. (1986) · Nature · doi:10.1038/320454a0 · Cited by 2,400
Human fibroblasts release reactive oxygen species in response to interleukin-1 or tumour necrosis factor-α
Meier, B., Radeke, H. H., Selle, S., Younes, M., Sies, H., Resch, K., & Habermehl, G. (1989) · Biochemical Journal · doi:10.1042/bj2630539 · Cited by 650
Modulation of fibroblast proliferation by oxygen free radicals
Murrell, G. A. C., Francis, M. J. O., & Bromley, L. (1990) · Biochemical Journal · doi:10.1042/bj2650659 · Cited by 625
NADH oxidoreductase is a major source of superoxide anion in bovine coronary artery endothelium
Mohazzab, K. M., Kaminski, P. M., & Wolin, M. S. (1994) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1994.266.6.h2568 · Cited by 536
Inhibition of macrophage and endothelial cell nitric oxide synthase by diphenyleneiodonium and its analogs 1
Stuehr, D. J., Fasehun, O. A., Kwon, N. S., Gross, S. S., Gonzalez, J. A., Levi, R., & Nathan, C. (1991) · The FASEB Journal · doi:10.1096/fasebj.5.1.1703974 · Cited by 465
A redox-based O2 sensor in rat pulmonary vasculature.
Archer, S. L., Huang, J., Henry, T., Peterson, D., & Weir, E. K. (1993) · Circulation Research · doi:10.1161/01.res.73.6.1100 · Cited by 362
Lucigenin chemiluminescence in the assessment of neutrophil superoxide production
Gyllenhammar, H. (1987) · Journal of Immunological Methods · doi:10.1016/0022-1759(87)90461-3 · Cited by 355
The particulate superoxide-forming system from human neutrophils. Properties of the system and further evidence supporting its participation in the respiratory burst.
BABIOR, B. M., Curnutte, J. T., & McMurrich, B. J. (1976) · Journal of Clinical Investigation · doi:10.1172/jci108553 · Cited by 348
Release of intact endothelium-derived relaxing factor depends on endothelial superoxide dismutase activity
Mügge, A., Elwell, J. H., Peterson, T. E., & Harrison, D. G. (1991) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1991.260.2.c219 · Cited by 314

Show all 24 references

Sorted by citations

Items 201–300 of 302

Chronic ethanol consumption increases vascular oxidative stress and the mortality induced by sub-lethal sepsis: Potential role of iNOS
Ceron, C. S., do Vale, G. T., Simplicio, J. A., Ricci, S. T., Martinis, B. S. D., de Freitas, A., & Tirapelli, C. R. (2018) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2018.02.008 · Cited by 27
Reactive oxygen species cause endothelial dysfunction in chronic flow overload
Lu, X., Guo, X., Wassall, C. D., Kemple, M. D., Unthank, J. L., & Kassab, G. S. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00786.2009 · Cited by 27
Effect of chronic apocynin treatment on nitric oxide and reactive oxygen species production in borderline and spontaneous hypertension
Pecháňová, O., Jendeková, L., & Vranková, S. (2009) · Pharmacological Reports · doi:10.1016/s1734-1140(09)70013-1 · Cited by 27
Electron spin resonance detection of extracellular superoxide anion released by cultured endothelial cells
Souchard, J., Barbacanne, M.-A., Margeat, E., Maret, A., Nepveu, F., & Arnal, J. (1998) · Free Radical Research · doi:10.1080/10715769800300491 · Cited by 27
Nitric oxide attenuates insulin- or IGF-I-stimulated aortic smooth muscle cell motility by decreasing H2O2levels: essential role of cGMP
Zhuang, D., Ceacareanu, A. C., Lin, Y., Ceacareanu, B., Dixit, M., Chapman, K. E., Waters, C. M., Rao, G. N., & Hassid, A. (2004) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01118.2003 · Cited by 27
Felodipine Inhibits Free-Radical Production by Cytokines and Glucose in Human Smooth Muscle Cells
Hishikawa, K., & Lüscher, T. F. (1998) · Hypertension · doi:10.1161/01.hyp.32.6.1011 · Cited by 27
Complications of type 1 diabetes: new molecular findings
Stirban, A. O., Rosen, P., & Tschoepe, D. (2008) · Mount Sinai Journal of Medicine A Journal of Translational and Personalized Medicine · doi:10.1002/msj.20057 · Cited by 26
Melatonin prevents overproduction of reactive oxygen species and vascular dysfunction induced by cyclophosphamide
Pimenta, G. F., Awata, W. M. C., Orlandin, G. G., da Silva-Neto, J. A., Assis, V. O., da Costa, R. M., Bruder-Nascimento, T. B., Tostes, R. C., & Tirapelli, C. R. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122361 · Cited by 25
Sildenafil Protects Endothelial Cells From Radiation-Induced Oxidative Stress
Wortel, R. C., Mizrachi, A., Li, H., Markovsky, E., Enyedi, B., Jacobi, J. M., Brodsky, O., Cao, J., Lippert, A. R., Incrocci, L., et al. (2019) · The Journal of Sexual Medicine · doi:10.1016/j.jsxm.2019.08.015 · Cited by 25
Tyrosine nitration in blood vessels occurs with increasing nitric oxide concentration
Amirmansour, C., Vallance, P. J., & Bogle, R. (1999) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0702590 · Cited by 25
The Presence and Localization of Melatonin Receptors in the Rat Aorta
Schepelmann, M., Molčan, Ľ., Uhrova, H., Zeman, M., & Ellinger, I. (2011) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-011-9727-9 · Cited by 24
NADPH-Induced Contractions of Mouse Aorta Do Not Involve NADPH Oxidase: A Role for P2X Receptors
Judkins, C. P., Sobey, C. G., Dang, T. T., Miller, A. A., Dusting, G. J., & Drummond, G. R. (2006) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.105.096610 · Cited by 24
Antioxidants prevent high-d-glucose-enhanced endothelial Ca2+/cGMP response by scavenging superoxide anions
Graier, W. F., Simecek, S., Hoebel, B. G., Wascher, T. C., Dittrich, P., & Kostner, G. M. (1997) · European Journal of Pharmacology · doi:10.1016/s0014-2999(96)00989-2 · Cited by 23
Oxidative Stress and Vascular Disease
Behrendt, D., & Ganz, P. (2007) · Wiley eBooks · doi:10.1002/9780470988473.ch10 · Cited by 23
NAD(P)H Oxidases in Coronary Artery Disease
Arora, S., Vaishya, R., Dabla, P. K., & Singh, B. M. (2010) · Advances in clinical chemistry · doi:10.1016/s0065-2423(10)50004-0 · Cited by 22
Modulatory role of the adventitia on noradrenaline and angiotensin II responsesRole of endothelium and AT2 receptors
Somoza, B., González, M. B. V., GONZALEZ, J., Abderrahim, F., Arribas, S. M., & Fernández‐Alfonso, M. S. (2004) · Cardiovascular Research · doi:10.1016/j.cardiores.2004.10.007 · Cited by 22
Superoxide generation of phagocytes and nonphagocytic cells
Meier, B. (2001) · PROTOPLASMA · doi:10.1007/bf01289420 · Cited by 21
Prevention of Impairment of Cerebral Blood Flow Autoregulation During Acute Stage of Subarachnoid Hemorrhage by Gene Transfer of Cu/Zn SOD-1 to Cerebral Vessels
Shin, H. K., Lee, J. H., Kim, C. D., Kim, Y. K., Hong, J. Y., & Hong, K. W. (2003) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200301000-00011 · Cited by 19
Superoxide Anion Generation, Superoxide Dismutase Activity, and Nitric Oxide Release in Human Internal Mammary Artery and Saphenous Vein Segments
Schmalfuss, C. M., Chen, L. Y., Bott, J. N., Staples, E. D., & Mehta, J. L. (1999) · Journal of Cardiovascular Pharmacology and Therapeutics · doi:10.1177/107424849900400406 · Cited by 18
Pulmonary reduction of an intravascular redox polymer
Audi, S. H., Bongard, R. D., Okamoto, Y., Merker, M. P., Roerig, D. L., & DAWSON, C. A. (2001) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.2001.280.6.l1290 · Cited by 18
Effects of Hyperglycemia on Vascular Smooth Muscle Ca2+Signaling
El‐Najjar, N., Kulkarni, R., Nader, N., Hodeify, R. F., & Machaca, K. (2017) · BioMed Research International · doi:10.1155/2017/3691349 · Cited by 17
A Review of the Actions of Endogenous and Exogenous Vasoactive Substances during the Estrous Cycle and Pregnancy in Rats
Jaimes, L., Vinet, R., Knox, M., Morales, B., Benites, J. F., Laurido, C., & Martínez, J. L. (2019) · Animals · doi:10.3390/ani9060288 · Cited by 18
Lung Injury and Oxidoreductases
Hoidal, J. R., Xu, P., Huecksteadt, T. P., Sanders, K. A., Pfeffer, K. D., & Sturrock, A. (1998) · Environmental Health Perspectives · doi:10.1289/ehp.98106s51235 · Cited by 17
Inhibition of geranylgeranyltransferase I decreases generation of vascular reactive oxygen species and increases vascular nitric oxide production1
Zuckerbraun, B. S., Barbato, J. E., Hamilton, A. D., Sebti, S. M., & Tzeng, E. (2004) · Journal of Surgical Research · doi:10.1016/j.jss.2004.10.022 · Cited by 17
Multiple actions of lysophosphatidylcholine in human Jurkat T cells1
Im, Y.-J., Lee, Y.-K., Chung, H., & Im, D. (2006) · Acta Pharmacologica Sinica · doi:10.1111/j.1745-7254.2006.00339.x · Cited by 17
Relationship between Phospholipase D Activation and Endothelial Vasomotor Dysfunction in Rabbit Aorta
Cox, D. A., & Cohen, M. L. (1997) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)36994-0 · Cited by 17
Role of superoxide and thromboxane receptors in acute angiotensin II-induced vasoconstriction of rabbit vessels
Pfister, S. L., Nithipatikom, K., & Campbell, W. B. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01135.2010 · Cited by 16
Enhanced vascular production of superoxide in OLETF rat after the onset of hyperglycemia
Kim, I. J., Kim, Y. K., Son, S. M., Hong, K. W., & Kim, C. D. (2003) · Diabetes Research and Clinical Practice · doi:10.1016/s0168-8227(02)00278-4 · Cited by 16
Apocynin alters redox signaling in conductance and resistance vessels of spontaneously hypertensive rats
Graton, M. E., Potje, S. R., Troiano, J. A., do Vale, G. T., Perassa, L. A., Nakamune, A. C. D. M. S., Tirapelli, C. R., Bendhack, L. M., & Antoniali, C. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.12.026 · Cited by 16
In human hypercholesterolemia increased reactivity of vascular smooth muscle cells is due to altered subcellular Ca2+ distribution
Fleischhacker, E., Esenabhalu, V. E., Holzmann, S., Skrabal, F., Koidl, B., Kostner, G. M., & Graier, W. F. (2000) · Atherosclerosis · doi:10.1016/s0021-9150(99)00290-7 · Cited by 16
Gene transfer of Cu/Zn SOD to cerebral vessels prevents FPI-induced CBF autoregulatory dysfunction
Kim, C. D., Shin, H. K., Lee, H. S., Lee, J. H., Lee, T. H., & Hong, K. W. (2002) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00590.2001 · Cited by 16
Ethanol consumption favors pro-contractile phenotype of perivascular adipose tissue: A role for interleukin-6
Simplicio, J. A., Dourado, T. M. H., Awata, W. M. C., do Vale, G. T., Dias, V. R., Barros, P. R., Martinis, B. S. D., Tostes, R. C., & Tirapelli, C. R. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121526 · Cited by 15
Ethanol and cyclophosphamide induce similar nephrotoxic effects: possible role for Nox4 and superoxide
Sousa, A. H., do Vale, G. T., da Silva, C. B. P., Awata, W. M. C., Pinheiro, L. C., & Tirapelli, C. R. (2020) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2020-0246 · Cited by 15
Oxidative stress, nitric oxide and prostaglandin E2 levels in the gastrointestinal tract of aging rats
Mármol, F., Sánchez, J., López, D., Martínez, N., Mitjavila, M. T., & Puig‐Parellada, P. (2009) · Journal of Pharmacy and Pharmacology · doi:10.1211/jpp.61.02.0009 · Cited by 15
Role of NADPH Oxidase in Cytomegalovirus-Induced Proliferation of Human Coronary Artery Smooth Muscle Cells
Dhaunsi, G. S., Kaur, J., & Turner, R. B. (2003) · Journal of Biomedical Science · doi:10.1007/bf02256111 · Cited by 15
Maniçoba, a quercetin-rich Amazonian dish
Kubo, I., Masuoka, N., Nihei, K., & Burgheim, B. (2006) · Journal of Food Composition and Analysis · doi:10.1016/j.jfca.2006.02.007 · Cited by 15
Endothelial Function: Strategies for Early Intervention
Verhaar, M. C., & Rabelink, T. J. (1998) · Cardiovascular Drugs and Therapy · doi:10.1023/a:1007737412395 · Cited by 15
Cellfood™ improves respiratory metabolism of endothelial cells and inhibits hypoxia-induced reactive oxygen species (ros) generation.
Ferrero, E., Fulgenzi, A., Belloni, D., Foglieni, C., & Ferrero, M. E. (2011) · PubMed · Cited by 14
Free radical production in aortic rings from rats fed a fish oil-rich diet
López, D., Caballero, C., Sánchez, J., Puig‐Parellada, P., & Mitjavila, M. T. (2001) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2001.280.6.h2929 · Cited by 14
Essential role of protein kinase G and decreased cytoplasmic Ca2+levels in NO-induced inhibition of rat aortic smooth muscle cell motility
Zhuang, D., Ceacareanu, A. C., Ceacareanu, B., & Hassid, A. (2004) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01031.2004 · Cited by 13
Angiotensin receptor antagonists delay nitric oxide-deficient stroke in stroke-prone rats
Ahmad, S. (1997) · European Journal of Pharmacology · doi:10.1016/s0014-2999(97)01089-3 · Cited by 12
Ethanol withdrawal increases blood pressure and vascular oxidative stress: a role for angiotensin type 1 receptors
Gonzaga, N. A., do Vale, G. T., Parente, J. M., Yokota, R., Martinis, B. S. D., Casarini, D. E., de Castro, M. M., & Tirapelli, C. R. (2018) · Journal of the American Society of Hypertension · doi:10.1016/j.jash.2018.03.012 · Cited by 12
The Etiology of Hypertension in the Metabolic Syndrome Part Three: The Regulation and Dysregulation of Blood Pressure
Publisher, B. S. P. B. S. (2006) · Current Vascular Pharmacology · doi:10.2174/157016106778521643 · Cited by 12
Oxidative stress and the endothelium
Wadsworth, R. M. (2007) · Experimental Physiology · doi:10.1113/expphysiol.2007.038687 · Cited by 12
Caveolin and MAP kinase interaction in angiotensin II preconditioning of the myocardium
Das, M., Das, S., & Das, D. K. (2007) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2007.00067.x · Cited by 12
Retracted
Oxygenated Perfluorochemicals Improve Cell Survival during Reoxygenation by Pacifying Mitochondrial Activity
Arab, A., Kummerer, K., Wang, J., Bode, C., & Hehrlein, C. (2008) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.133710 · Cited by 11
Functional Expression of NAD(P)H Oxidase p47 in Lung Microvascular Endothelial Cells
Murphy, H. S., Yu, C., & Quddus, J. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.3848 · Cited by 11
Freie Radikale in Pathogenese und Therapie von entzündlichen Erkrankungen des Bronchialsystems
Hippeli, S., Graßmann, J., Dornisch, K., Rohnert, U., & Elstner, E. F. (2000) · Springer eBooks · doi:10.1007/978-3-642-59770-1_1 · Cited by 10
Transient Hyperoxic Reoxygenation Reduces Cytochrome c Oxidase Activity by Increasing Superoxide Dismutase and Nitric Oxide
Arab, A., Wang, J., Bausch, K., von Schmädel, K., Bode, C., & Hehrlein, C. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.053181 · Cited by 10
Acute Ethanol Intake Induces NAD(P)H Oxidase Activation and Rhoa Translocation in Resistance Arteries
Simplicio, J. A., Hipólito, U. V., do Vale, G. T., Callera, G. E., Pereira, C. A., Touyz, R. M., Tostes, R. C., & Tirapelli, C. R. (2016) · Arquivos Brasileiros de Cardiologia · doi:10.5935/abc.20160147 · Cited by 9
Phenolic Combination and Comparison of Antioxidant Activity in Three Different Alcoholic Extracts of Dracocephalum moldavica L.
Aslanıpour, B., Heidari, R., & Farnad, N. (2017) · Turkish Journal of Agriculture - Food Science and Technology · doi:10.24925/turjaf.v5i3.199-206.812 · Cited by 9
Molecular Sensors for Cardiovascular Homeostasis
Wang, D. H. (2007) · Springer eBooks · doi:10.1007/978-0-387-47530-1 · Cited by 9
Nitric oxide modulates angiotensin II-induced endothelial vasoconstrictor prostanoid release
Jerez, S. J., de Bruno, M. P., & Coviello, A. (2005) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2005.07.030 · Cited by 9
Efficacy and safety of angiotensin-converting enzyme inhibitors or angiotensin receptor blockers for IgA nephropathy in children
de Castro, P. A. S. V., Bitencourt, L., Pereira, B. W. S., Lima, A. Q. R., Hermida, H. S., Neto, C. R. M., Mestriner, M. D., & Silva, A. C. S. E. (2021) · Pediatric Nephrology · doi:10.1007/s00467-021-05316-0 · Cited by 8
Modulation of Reactive Oxygen Species and Collagen Synthesis by Angiotensin II in Cardiac Fibroblasts
Lijnen, P. J. (2011) · The Open Hypertension Journal · doi:10.2174/1876526201104010001 · Cited by 7
Intimal plaque development and oxidative stress in cholesterol‐induced atherosclerosis in New Zealand rabbits
Heinle, H., Brehme, U., Friedemann, G., Frey, J. ‐., Wolf, A. T., Kelber, O., Weiser, D., Schmahl, F. W., Lang, F. J. W., & Schneider, W. (2002) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2002.01024.x · Cited by 7
Effects of angiotensin I and angiotensin II in blood vessels: greater influence of converting enzyme activity in the rabbit basilar artery
Zerrouk, A., Auguet, M., Delaflotte, S., & Chabrier, P. (1996) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/bf00168438 · Cited by 7
Things have changed: cell cycle dysregulation and smooth muscle cell dysfunction in atherogenesis
Patterson, C. (2002) · Ageing Research Reviews · doi:10.1016/s1568-1637(01)00002-2 · Cited by 6
Ethanol Withdrawal Alters the Oxidative State of the Heart Through AT1-Dependent Mechanisms
Assis, V. O., Gonzaga, N. A., da Silva, C. B. P., Pereira, L. C., Padovan, C. M., & Tirapelli, C. R. (2019) · Alcohol and Alcoholism · doi:10.1093/alcalc/agz101 · Cited by 5
The Enigmatic Vascular NOX: From Artifact to Double Agent of Change
Pagano, P. J., & Cifuentes-Pagano, E. (2021) · Hypertension · doi:10.1161/hypertensionaha.120.13897 · Cited by 6
Self-citation
Interleukin-10 limits the initial steps of the cardiorenal damage induced by ethanol consumption
da Silva, C. B. P., Gómez, J. P. S., do Vale, G. T., Simplicio, J. A., Gonzaga, N. A., & Tirapelli, C. R. (2020) · Life Sciences · doi:10.1016/j.lfs.2019.117239 · Cited by 4
Atherosclerosis, Oxidative Stress, and Endothelial Function
Keaney, J. F. (2000) · Developments in cardiovascular medicine · doi:10.1007/978-1-4615-4649-8_9 · Cited by 4
Extracellular and intracellular arachidonic acid-induced contractions in rat aorta
Filipeanu, C. M., Brailoiu, E., Petrescu, G., & Nelemans, S. A. (1998) · European Journal of Pharmacology · doi:10.1016/s0014-2999(98)00180-0 · Cited by 4
Nebivolol prevents redox imbalance and attenuates bladder dysfunction induced by cyclophosphamide in mice
Jesus, C., Pimenta, G. F., de Oliveira, M. G., Dourado, T. M. H., Antunes, E., & Tirapelli, C. R. (2024) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2024-0064 · Cited by 3
The Fibroblast and Nitric Oxide
Brecher, P. I. (2000) · doi:10.1007/978-1-59259-002-5_11 · Cited by 3
Antioxidants and Endothelium-Derived Nitric Oxide Action
Huang, A., & Keaney, J. F. (2000) · Humana Press eBooks · doi:10.1007/978-1-59259-002-5_26 · Cited by 3
DETECTION OF SUPEROXIDE ANION RELEASED EXTRACELLULARLY BY ENDOTHELIAL CELLS USING CYTOCHROME C REDUCTION, ESR, FLUORESCENCE AND LUCIGENIN-ENHANCED CHEMILUMINESCENCE TECHNIQUES
Barbacanne, M.-A., Souchard, J., Darblade, B., Iliou, J., Nepveu, F., Pipy, B., Bayard, F., & Arnal, J. (2001) · Elsevier eBooks · doi:10.1016/b978-0-444-50957-4.50025-9 · Cited by 2
Expression of intracellular adhesion molecule–1 linking superoxide to mobilization of granulocytes and macrophages after periarterial blood in rat femoral artery: effect of rebamipide
Choi, J. M., Kim, C. D., & Hong, K. W. (2000) · Neurosurgical FOCUS · doi:10.3171/foc.2000.8.5.5 · Cited by 2
Mechanisms of vascular disease
Li, Y., Faraci, F. M., Heistad, D. D., Lamping, K. G., Rahmouni, K., & Sigmund, C. D. (2014) · doi:10.17077/etd.7otf4nv9 · Cited by 2
Other Factors in Endothelial Cell Dysfunction in Hypertension and Diabetes
Cohen, R. A., & Pagano, P. J. (1997) · Springer eBooks · doi:10.1007/978-3-642-60811-7_4 · Cited by 2
Self-citation
ROS and Precision Medicine in Lifestyle Diseases
Gupta, P. K., Chaudhari, Y., Joseph, A., Sinha, S., Rashid, A., & Prabhakar, P. K. (2025) · Advances in medical diagnosis, treatment, and care (AMDTC) book series · doi:10.4018/979-8-3693-7919-6.ch013 · Cited by 1
Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats
Aykan, D. A., Seyithanoğlu, M., Eser, N., Tanrıverdi, B., & Yaman, S. (2019) · Medical Bulletin of Haseki · doi:10.4274/haseki.galenos.2019.5525 · Cited by 1
Mechanisms of Cardioprotection against Ischemia Reperfusion Injury
Singh, R. B., & Dhalla, N. S. (2004) · Progress in experimental cardiology · doi:10.1007/978-1-4615-0453-5_23 · Cited by 1
Improvement in Endothelial Function by Angiotensin-converting Enzyme Inhibition and Vitamin C in Essential Hypertension
On, Y. K., Chung, W. Y., Chae, I. H., Kim, C., Sohn, D. W., Oh, B., Lee, M. M., Park, Y. B., & Choi, Y. S. (2001) · Korean Circulation Journal · doi:10.4070/kcj.2001.31.4.411 · Cited by 1
UNIVERSIDADE ESTADUAL PAULISTA "JÚLIO DE
Filho, M. (2011) · Cited by 1
Factors regulating arteriolar tone during microvascular growth
Samora, J. B. (2007) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.4290 · Cited by 1
Role of Nitric Oxide in Vasomotor Regulation
Cohen, R. A. (2000) · doi:10.1007/978-1-59259-002-5_7 · Cited by 1
Self-citation
Nitric Oxide Regulation of Membrane and Lipoprotein Oxidation in the Vasculature
Freeman, B. Α., Eiserich, J. P., & O’Donnell, V. B. (1998) · Springer eBooks · doi:10.1007/978-1-4757-2907-8_6 · Cited by 1
A resposta contrátil induzida pela fenilefrina é modulada pelo peróxido de hidrogênio em aorta de ratos hipertensos renais
Silva, B. R. (2013) · doi:10.11606/t.17.2013.tde-22102013-151639
Mecanismos celulares ativados por agonistas adrenérgicos em aorta de ratos hipertensos renais com disfusão endotelial
Bocalon, A. C. C. C. (2014) · doi:10.11606/d.60.2014.tde-30102014-134300
Western Blot und realtime PCR- basierte Identifizierung möglicher Hypertonie assoziierter Gene an einem definiertem Hypotoniemodell an Wistar-Kyoto Ratten
Furundzija, V. (2008) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-12773
The Structural and Functional Changes of Blood Vessels during Aging
Rätsep, M. T. (2011)
Untersuchungen zu den Mechanismen und den Auswirkungen von oxidativem Stress im Aortengewebe von Kaninchen, Oryctolagus cunigulus, Linnè 1758
Oelze, M. W. (2003)
Rational Design and Therapeutic Potential of a Novel Nox1 Inhibitor for the Treatment of Pulmonary Hypertension: In Vitro and In Vivo Effects of Nox1 Inhibition
Ranayhossaini, D. (2014) · D-Scholarship@Pitt (University of Pittsburgh)
NADPH Oxidase as a Mechanistic Link Between Erectile Dysfunction Peripheral and Coronary Endothelial Dysfunction in Obesity
La, F. J. D. (2012)
Hemodynamic Forces-Induced Biochemical Changes in Aortic wall: Effect on Redox State of the Tissue
Husain, S. Y., Ray, A. R., & Ray, A. R. (2010) · American Journal of Biomedical Sciences · doi:10.5099/aj100400295
Study of Renal Tubular Cell Damage by Oxidative Stress in Potassium Deficient Rats
Suwannachot, N. (2007) · Khon Kaen University Journal (Graduate Studies) · doi:10.5481/kkujgs.2007.07.9
Protection of vascular nitric oxide by superoxide dismutase mimetics
MacKenzie, A. R. (1998) · Enlighten: Theses (The University of Glasgow) · doi:10.5525/gla.thesis.71832
Endothelial injury in cardiac transplantation : the role of endothelin antagonism and protein kinases.
Ramzy, D. (2008) · TSpace (University of Toronto)
Oxygen radical generation by lymphoblast NADPH oxidase in hypertension
Pettit, A. I. (2006) · Leicester Research Archive (University of Leicester)
Participação do TNF-a nas disfunções vasculares induzidas pelo consumo crônico de etanol: envolvimento do tecido adiposo perivascular
Simplicio, J. A. (2018) · doi:10.11606/t.17.2018.tde-17042018-160849
Introduction
Haber, A. (2012) · Springer theses · doi:10.1007/978-3-642-30328-9_1
NO and the Vasculature: Where Does It Come from and What Does It Do?
Andrews, K. L., Triggle, C. R., & Ellis, A. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/1-4020-7960-5_2
Die Rolle des Toll-like Rezeptors 4 bei der Entstehung von Bluthochdruck und der Kontraktilität von Widerstandsgefäßen
Eißler, R. (2011) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.14426
Essential Role of Adventitial Reactive Oxygen Species in Vascular Function 54
Wang, H. D., & Chapman, A. (2014)
A catalytically active and recyclable bioelastomer inspired by metalloenzymes
Latvis, C., Garren, M. R. S., Wright, N. S., Ge, K., Li, Z., Shao, H., Pollock, C. J., Handa, H., Brisbois, E. J., Herck, S. V., et al. (2026) · Bioactive Materials · doi:10.1016/j.bioactmat.2026.02.053
Rôle du stress oxydant en période néonatale dans l'hypertension artérielle et la dysfonction vasculaire et métabolique de l'adulte
Yzydorczyk, C. (2011) · theses.fr (ABES) · doi:10.70675/79493b0fz49ecz4151zad3ezc0d9f2e5d333
Effet d'un traitement périnatal avec un hypocholestérolémiant (cholestyramine) et/ou un antioxydant (vitamine E) sur le développement de l'athérosclérose chez la descendance adulte de souris déficientes en apolipoprotéine E
Habib, M. (2022) · theses.fr (ABES) · doi:10.70675/e634ffe7zc86dz4e0fzb03dz223ee5589a93
Exploration of transcriptional regulatory mechanisms at ZNF827 locus identified by several vascular diseases GWAS
Liu, Y. (2024) · doi:10.70675/d40f40d5zb8e3z486ezac81z874df31a9d5c
Unmyelinated Aortic Baroreceptor Activity is Reduced in a Rabbit Model of Atherosclerosis
Bolter, C. P., & Turner Michael, J. (2026) · IgMin Research · doi:10.61927/igmin340

Authors: Pagano, P. J., Ito, Y., Tornheim, K., Gallop, P. M., Tauber, A. I., & Cohen, R. A.
Affiliations: Robert Dawson Evans Department of Clinical Research, UniversityMedical Center, Boston 02118, USA.
ORCID: Pagano, P. J.
Ito, Y.
Tauber, A. I.
Cohen, R. A.
Venue: American Journal of Physiology-Heart and Circulatory Physiology
Publisher: American Physiological Society
Published: 1995-06-01
Volume: 268
Issue: 6
Pages: H2274-H2280
ISSN: 0363-6135 (ISSN-L)
1522-1539
DOI: 10.1152/ajpheart.1995.268.6.h2274
OpenAlex: W2219200263
Cited by: 302
References: 24
Citations by year: 2026: 2 · 2025: 2 · 2024: 2 · 2023: 2 · 2022: 1 · 2021: 2 · 2020: 3 · 2019: 6 · 2018: 6 · 2017: 4 · 2016: 3 · 2015: 7 · 2014: 7 · 2013: 6 · 2012: 5
FWCI: 7.50
Type: journal article
Language: en
Open access: closed
Locations: American Journal of Physiology-Heart and Circulatory Physiology (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health (5p50hl047124-04, 5r01hl038731-08)
National Heart, Lung, and Blood Institute (HL-38731, R01HL031607, HL 47124, HL31607)
Topics: Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
Keywords: NADPH oxidase, superoxide, rabbit aorta, vascular smooth muscle, diphenyleneiodonium, diethyldithiocarbamate, chemiluminescence, xanthine oxidase, mitochondrial NADH dehydrogenase, vascular tone
MeSH terms: Animals, Aorta, Thoracic, Ditiocarb, Kinetics, Male, Muscle, Smooth, Vascular, NADH, NADPH Oxidoreductases, NADP, Onium Compounds, Oxypurinol, Rabbits, Rotenone, Subcellular Fractions, Superoxides, Thiophenes, NADPH Oxidases, In Vitro Techniques

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

An NADPH oxidase superoxide-generating system in the rabbit aorta

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks