Cited by 293Nitric Oxide and Endothelin EffectsNeutrophil, Myeloperoxidase and Oxidative MechanismsRedox biology and oxidative stress

The DOI matches its Crossref record; 207 of the 211 references it cites were found in a registry or an index.

Modulation of leukocyte–endothelial interactions by reactive metabolites of oxygen and nitrogen: relevance to ischemic heart disease

Grisham, Matthew B., Granger, D.Neil, Lefer, David J.·1998·Free Radical Biology and Medicine

DOI 10.1016/s0891-5849(98)00094-x

Open this paper in CoChat — free account

Abstract

Ischemia and reperfusion (I/R) are thought to play an important role in the pathophysiology of ischemic diseases of the heart. It is now well appreciated that leukocyte-endothelial cell interactions are important determinants for I/R-induced microvascular injury and dysfunction. There is a growing body of experimental data to suggest that reactive metabolites of oxygen and nitrogen are important physiological modulators of leukocyte-endothelial cell interactions. A number of investigators have demonstrated that I/R enhances oxidant production within the microcirculation resulting in increases in leukocyte adhesion and transendothelial cell migration. Several other studies have shown that exogenous nitric oxide (NO) donors may attenuate leukocyte and platelet adhesion and/or aggregation in a number of different inflammatory conditions including I/R. The objective of this review is to discuss the physiological chemistry of reactive metabolites of oxygen and nitrogen with special attention given to those interactions that may modulate leukocyte-endothelial cell interactions, provide an overview of the evidence implicating reactive metabolites of oxygen and nitrogen as modulators of leukocyte-endothelial cell interactions in vivo, and discuss how these mechanisms may be involved in the pathophysiology of ischemic heart disease.

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

Crossref · 10.1016/s0891-5849(98)00094-x

Cites

207 of 207 references verified0 citation errors · 0 not checkable

Statistics

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Free radicals in biology and medicine
Gutteridge, J. M. C. (1991) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(91)90478-o · Cited by 17,178
Apparent hydroxyl radical production by peroxynitrite: Implications for endothelial injury from nitric oxide and superoxide
Beckman, J. S., Beckman, T. W., Chen, J., Marshall, P. A., & Freeman, B. A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.4.1620 · Cited by 7,029
Free Radicals in Biology and Medicine
Land, E. J. (1990) · International Journal of Radiation Biology · doi:10.1080/09553009014552071 · Cited by 4,871
Nitric oxide: an endogenous modulator of leukocyte adhesion.
Kubes, P., Suzuki, M., & Granger, D. N. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.11.4651 · Cited by 3,036
Self-citation
Peroxynitrite oxidation of sulfhydryls.
Radí, R., Beckman, J. S., Bush, K., & Freeman, B. Α. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)64313-7 · Cited by 2,492
Interleukin-8 and related chemotactic cytokines--CXC and CC chemokines.
Baggiolini, M., Dewald, B., & Moser, B. (1994) · PubMed · Cited by 2,232
Peroxynitrite-induced membrane lipid peroxidation: The cytotoxic potential of superoxide and nitric oxide
Radí, R., Beckman, J. S., Bush, K. M., & Freeman, B. Α. (1991) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(91)90224-7 · Cited by 2,201
The reaction of NO with superoxide
Huie, R. E., & Padmaja, S. (1993) · Free Radical Research Communications · doi:10.3109/10715769309145868 · Cited by 2,121
Structure, Regulation and Function of NF-kappaB
Siebenlist, U. K., Franzoso, G., & Brown, K. D. (1994) · Annual Review of Cell Biology · doi:10.1146/annurev.cb.10.110194.002201 · Cited by 2,086
The wavefront phenomenon of ischemic cell death. 1. Myocardial infarct size vs duration of coronary occlusion in dogs.
Reimer, K. A., Lowe, J. E., Rasmussen, M. M., & Jennings, R. B. (1977) · Circulation · doi:10.1161/01.cir.56.5.786 · Cited by 1,944

Show all 211 references

Research works printed but not linked: 15

Gaboury, 1993, Nitric oxide prevents leukocyte adherence, Am. J. Physiol., 265, H862
Paller, 1988, Hemoglobin and myoglobin-induced acute renal failure in rats, Am. J. Physiol., 255, F539
Koppenol, 1996, Synthesis of peroxynitrite, Meth. Enz., 269, 296
Asako, 1992, Indomethacin-induced leukocyte adhesion in mesenteric venules, Am. J. Physiol., 262, G903
Inauen, 1990, Anoxia-reoxygenation-induced, neutrophil-mediated endothelial cell injury, Am. J. Physiol., 259, H925
Milhoan, 1992, Hypoxia induces endothelial cells to increase their adherence for neutrophils, Am. J. Physiol., 263, H956
Manning, 1994, Transcription factor NF-κB, Annu. Rep. Med. Chem., 28, 235
Kurose, 1997, Ischemia/reperfusion-induced microvascular dysfunction, Am. J. Physiol., 272, H2976
Kubes, 1993, Nitric oxide-induced microvascular permeability alterations, Am. J. Physiol., 265, H1910
Seekamp, 1993, Requirements for neutrophil products and l-arginine in ischemia-2Dreperfusion injury, Am. J. Pathol., 142, 1
Ma, 1993, Dimished basal nitric oxide release after myocardial ischemia and reperfusion promotes neutrophil adherence to coronary endothelium, Circ. Res., 72, 403, 10.1161/01.RES.72.2.403 · DOI
Mehta, 1989, Attenuated coronary relaxation after reperfusion, Am. J. Physiol., 257, H1240
Rubanyi, 1986, Superoxide anions and hyperoxia inactivate endothelium-derived relacing factor, Am. J. Physiol., 250, H822
Shirato, 1988, Superoxide dismutase (single dose) delays rather than prevents necrosis in reperfused rabbit heart, FASEB J, 2, A918
Mathies, 1992, Role of l-arginine–nitric oxide pathway in myocardial reoxygenation injury, Am. J. Physiol., 262, H616

Sorted by citations

Items 101–200 of 292

Inhibition of sickle red cell adhesion and vasoocclusion in the microcirculation by antioxidants
Kaul, D. K., Liu, X.-D., Zhang, X., Ma, L., Hsia, C. J. C., & Nagel, R. L. (2006) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01096.2005 · Cited by 57
A zebrafish assay for identifying neuroprotectants in vivo
Parng, C., Ton, C., Lin, Y., Roy, N. M., & McGrath, P. (2006) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2006.04.003 · Cited by 58
Inhibiting matrix metalloproteinase-2 reduces protein release into coronary effluent from isolated rat hearts during ischemia-reperfusion
Fert‐Bober, J., León, H., Sawicka, J., Basran, R., Devon, R. M., Schulz, R., & Sawicki, G. (2008) · Basic Research in Cardiology · doi:10.1007/s00395-008-0727-y · Cited by 54
Absence of Poly(ADP-ribose) Polymerase-1 Alters Nuclear Factor-κB Activation and Gene Expression of Apoptosis Regulators after Reperfusion Injury
Zingarelli, B., Hake, P. W., O’Connor, M., Denenberg, A. G., Kong, S., & Aronow, B. J. (2003) · Molecular Medicine · doi:10.1007/bf03402179 · Cited by 54
EXSANGUINOUS METABOLIC SUPPORT PERFUSION???A NEW STRATEGY TO IMPROVE GRAFT FUNCTION AFTER KIDNEY TRANSPLANTATION1
Stubenitsky, B. M., Booster, M. H., Brasile, L., ARANEDA, D., Haisch, C. E., & Kootstra, G. (2000) · Transplantation · doi:10.1097/00007890-200010270-00024 · Cited by 52
Macrolide antibiotics improve chemotactic and phagocytic capacity as well as reduce inflammation in sulfur mustard-exposed monocytes
Gao, X., Ray, R., Xiao, Y., Ishida, K., & Ray, P. (2009) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2009.10.010 · Cited by 52
Nitric Oxide Donors Suppress Chemokine Production by Keratinocytes in Vitro and in Vivo
Giustizieri, M. L., Albanesi, C., Scarponi, C., Pità, O. D., & Girolomoni, G. (2002) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64416-1 · Cited by 52
Cardioprotective actions of endogenous IL-10 are independent of iNOS
Jones, S. P., Trocha, S. D., & Lefer, D. J. (2001) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2001.281.1.h48 · Cited by 52
Self-citation
Polyethylene microplastics are ingested and induce biochemical changes in Culex quinquefasciatus (Diptera: Culicidae) freshwater insect larvae
Malafaia, G., da Luz, T. M., Guimarães, A. T. B., & Araújo, A. P. D. C. (2020) · Ecotoxicology and Environmental contamination · doi:10.5132/eec.2020.01.10 · Cited by 50
Tonal nitric oxide and health--a free radical and a scavenger of free radicals.
Benz, D., Cadet, P., Mantione, K. J., Zhu, W. P., & Stefano, G. B. (2002) · PubMed · Cited by 51
Leukotriene B4 promotes reactive oxidant generation and leukocyte adherence during acute hypoxia
Steiner, D. R. S., González, N. C., & Wood, J. G. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.3.1160 · Cited by 51
Chronic effects of nano and microplastics on reproduction and development of marine copepod Tigriopus japonicus
Kim, K., Yoon, H., Choi, J. S., Jung, Y.-J., & Park, J. (2022) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2022.113962 · Cited by 50
Myoglobin-Catalyzed Tyrosine Nitration: No Need for Peroxynitrite
Kılınç, K., Kılınç, A., Wolf, R. E., & Grisham, M. B. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.5168 · Cited by 50
Self-citation
RETRACTED: Toxicity of polystyrene nanoplastics in dragonfly larvae: An insight on how these pollutants can affect bentonic macroinvertebrates
Guimarães, A. T. B., Rodrigues, A. S. D. L., Pereira, P. S., Silva, F. G., & Malafaia, G. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.141936 · Cited by 49
Retracted
Peroxynitrite-dependent modifications of tyrosine residues in hemoglobin. Formation of tyrosyl radical(s) and 3-nitrotyrosine
Pietraforte, D., Salzano, A. M., Marino, G., & Minetti, M. (2003) · Amino Acids · doi:10.1007/s00726-003-0021-0 · Cited by 48
Preconditioning protects endothelium by preventing ET-1-induced activation of NADPH oxidase and xanthine oxidase in post-ischemic heart
Duda, M. K., Konior, A., Klemenska, E., & Berȩsewicz, A. (2006) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2006.10.014 · Cited by 47
Cerebral Vasospasm After Aneurysmal Subarachnoid Hemorrhage and Traumatic Brain Injury
Izzy, S., & Muehlschlegel, S. (2013) · Current Treatment Options in Neurology · doi:10.1007/s11940-013-0278-x · Cited by 44
Prevention of aortic fibrosis byN-acetyl-seryl-aspartyl-lysyl-proline in angiotensin II-induced hypertension
Lin, C.-X., Rhaleb, N., Yang, X.-P., Liao, T., D’Ambrosio, M. A., & Carretero, O. A. (2008) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00481.2008 · Cited by 48
Regulation of protein function by S-nitrosation and S-glutathionylation: processes and targets in cardiovascular pathophysiology
Belcastro, E., Gaucher, C., Corti, A., Leroy, P., Lartaud, I., & Alfonso Pompella, C. (2017) · Biological Chemistry · doi:10.1515/hsz-2017-0150 · Cited by 48
Hepatocellular protection by nitric oxide or nitrite in ischemia and reperfusion injury
Abe, Y., Hines, I. N., Zibari, G. B., & Grisham, M. B. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.10.006 · Cited by 44
Self-citation
Purification and Characterization of NEIL1 and NEIL2, Members of a Distinct Family of Mammalian DNA Glycosylases for Repair of Oxidized Bases
Hazra, T. K., & MITRA, S. P. (2006) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(06)08003-7 · Cited by 42
Cytokine and Adhesion Molecule Expression in SCID Mice Reconstituted with CD4+ T Cells
Kawachi, S., Morise, Z., Jennings, S. R., Conner, E. M., Cockrell, A. S., Laroux, S., Chervenak, R. P., Wolcott, M., van der Heyde, H., Gray, L. T., et al. (2000) · Inflammatory Bowel Diseases · doi:10.1097/00054725-200008000-00003 · Cited by 42
Self-citation
Adhesion of flowing monocytes to hypoxia-reoxygenation-exposed endothelial cells: role of Rac1, ROS, and VCAM-1
Ng, C. K. D., Deshpande, S. S., Irani, K., & Alevriadou, B. R. (2002) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00301.2001 · Cited by 41
The Gastrointestinal Circulation
Kvietys, P. R. (2010) · Colloquium Series on Integrated Systems Physiology From Molecule to Function · doi:10.4199/c00009ed1v01y201002isp005 · Cited by 43
The molecular events underlying ischemia/reperfusion injury
Anaya‐Prado, R., & Toledo-Pereyra, L. H. (2002) · Transplantation Proceedings · doi:10.1016/s0041-1345(02)03471-1 · Cited by 39
Peroxynitrite in Myocardial Ischemia-Reperfusion Injury
Lalu, M. M., Wang, W., & Schulz, R. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/1-4020-7960-5_18 · Cited by 39
Knock out of neuronal nitric oxide synthase exacerbates intestinal ischemia/reperfusion injury in mice
Rivera, L. R., Pontell, L. J., Cho, H., Castelucci, P., Thacker, M., Poole, D. P., Frugier, T., & Furness, J. B. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1451-3 · Cited by 38
Effects of antioxidants and nitric oxide on TNF-α-induced adhesion molecule expression and NF-κB activation in human dermal microvascular endothelial cells
Jiang, M.-Z., Tsukahara, H., Ohshima, Y., Todoroki, Y., Hiraoka, M., Maeda, M., & Mayumi, M. (2004) · Life Sciences · doi:10.1016/j.lfs.2004.01.031 · Cited by 38
Platelets, Inflammation, and Atherothrombotic Neurovascular Disease: The Role of Endothelial Dysfunction
Blanco, M., Rodríguez‐Yáñez, M., Sobrino, T., Leira, R., & Castillo, J. (2005) · Cerebrovascular Diseases · doi:10.1159/000089355 · Cited by 37
Splanchnic ischaemia–reperfusion injury: mechanistic insights provided by mutant mice
Granger, D. N., Stokes, K. Y., Shigematsu, T., Cerwinka, W. H., Tailor, A., & Krieglstein, C. F. (2001) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2001.00888.x · Cited by 37
Self-citation
Role of calcitonin gene-related peptide in cerebral vasospasm, and as a therapeutic approach to subarachnoid hemorrhage
Kokkoris, S., Andrews, P., & Webb, D. J. (2012) · Frontiers in Endocrinology · doi:10.3389/fendo.2012.00135 · Cited by 35
In vitro culture and characterization of gene targeted mouse endothelium
Kevil, C. G., & Bullard, D. C. (2001) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2001.00901.x · Cited by 35
Effects of antioxidants and NO on TNF-α-induced adhesion molecule expression in human pulmonary microvascular endothelial cells
Jiang, M.-Z., Tsukahara, H., Hayakawa, K., Todoroki, Y., Tamura, S., Ohshima, Y., Hiraoka, M., & Mayumi, M. (2004) · Respiratory Medicine · doi:10.1016/j.rmed.2004.10.007 · Cited by 36
Peroxynitrite in Myocardial Ischemia-Reperfusion Injury
Lalu, M. M., Wang, W., & Schulz, R. (2002) · Heart Failure Reviews · doi:10.1023/a:1020766502316 · Cited by 34
Bothrops lanceolatus (Fer de lance) venom stimulates leukocyte migration into the peritoneal cavity of mice
Arruda, V. A., Guimarães, A. D. Q., Hyslop, S., de Araújo, P. M. F., Bon, C., & de Araújo, A. L. (2002) · Toxicon · doi:10.1016/s0041-0101(02)00238-6 · Cited by 34
A lipid peroxidation product 9-oxononanoic acid induces phospholipase A2 activity and thromboxane A2 production in human blood
Ren, R., Hashimoto, T., Mizuno, M., Takigawa, H., Yoshida, M., Azuma, T., & Kanazawa, K. (2013) · Journal of Clinical Biochemistry and Nutrition · doi:10.3164/jcbn.12-110 · Cited by 33
Differential mechanisms of hepatic vascular dysregulation with mild vs. moderate ischemia-reperfusion
Lee, S., Culberson, C., Korneszczuk, K., & Clemens, M. G. (2008) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00527.2007 · Cited by 33
Basal neutrophil function in human aging: Implications in endothelial cell adhesion
Nogueira‐Neto, J., Cardoso, A. S. C., Monteiro, H. P., Fonseca, F. L. A., Ramos, L. R., Junqueira, V. B. C., & Simon, K. (2016) · Cell Biology International · doi:10.1002/cbin.10618 · Cited by 32
Long noncoding RNA UCA1 inhibits ischaemia/reperfusion injury induced cardiomyocytes apoptosis via suppression of endoplasmic reticulum stress
Chen, J., Hu, Q. Z., Zhang, B., Liu, X., Yang, S., & Jiang, H. (2019) · Genes & Genomics · doi:10.1007/s13258-019-00806-w · Cited by 32
Polyethylene glycol and a novel developed polyethylene glycol-nitric oxide normalize arteriolar response and oxidative stress in ischemia-reperfusion
Bertuglia, S., Veronese, F. M., & Pasut, G. (2006) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01114.2005 · Cited by 32
Glomerular Endothelium Exhibits Enhanced Expression of Costimulatory Adhesion Molecules, CD80 and CD86, by Warm Ischemia/Reperfusion Injury in Rats
Satoh, S., Suzuki, A., Asari, Y., Sato, M., Kojima, N., Sato, T., Tsuchiya, N., Sato, K., Senoo, H., & Kato, T. (2002) · Laboratory Investigation · doi:10.1097/01.lab.0000029620.13097.19 · Cited by 31
Modulatory effects of hypercapnia on in vitro and in vivo pulmonary endothelial–neutrophil adhesive responses during inflammation
Liu, Y., Chacko, B. K., Ricksecker, A., Shingarev, R. A., Andrews, E. J., Patel, R. P., & Lang, J. D. (2008) · Cytokine · doi:10.1016/j.cyto.2008.06.016 · Cited by 30
Endothelial Signaling in Leukocyte Transmigration
Hordijk, P. L. (2003) · Cell Biochemistry and Biophysics · doi:10.1385/cbb:38:3:305 · Cited by 30
Suppression of Inducible Nitric Oxide Synthase Expression and Nitric Oxide Production by Macrolide Antibiotics in Sulfur Mustard‐Exposed Airway Epithelial Cells
Gao, X., Ray, R., Xiao, Y., & Ray, P. (2008) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/j.1742-7843.2008.00255.x · Cited by 29
Reduction of Postoperative Adhesions by N,O-Carboxymethylchitosan and Spermine NONOate in Rats.
Duran, B., Ak, D., Çetin, A., Güvenal, T., Çetin, M., & Imir, A. G. (2003) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.52.267 · Cited by 29
Cerebrovascular inflammation after brief episodic hypoxia: modulation by neuronal and endothelial nitric oxide synthase
Altay, T., Gonzales, E. R., Park, T. S., & Gidday, J. M. (2004) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00798.2003 · Cited by 29
Endothelial oxidative stress induced by serum from patients with severe trauma hemorrhage
Laplace, C., Huet, O., Vicaut, É., Ract, C., Martin, L., Benhamou, D., & Duranteau, J. (2005) · Intensive Care Medicine · doi:10.1007/s00134-005-2737-7 · Cited by 29
IkappaB-alpha expression following transient focal cerebral ischemia is modulated by nitric oxide
Greco, R., Mangione, A. S., Amantea, D., Bagetta, G., Nappi, G., & Tassorelli, C. (2010) · Brain Research · doi:10.1016/j.brainres.2010.11.071 · Cited by 28
c-Jun N-terminal kinase (JNK) repression during the inflammatory response? Just say NO
Hall, J. P., Merithew, E., & Davis, R. J. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.26.14022 · Cited by 28
Chlamydia trachomatis Inhibits Inducible NO Synthase in Human Mesenchymal Stem Cells by Stimulating Polyamine Synthesis
Lubad, M. A., Meyer, T. F., & Al‐Zeer, M. A. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1400377 · Cited by 27
Inhibitory effect of simvastatin on the TNF-α- and angiotensin II-induced monocyte adhesion to endothelial cells is mediated through the suppression of geranylgeranyl isoprenoid-dependent ROS generation
Park, S., Lee, J.-S., Ko, Y. J., Kim, A. R., Choi, M. K., Kwak, M., Choi, H. G., Yong, C. S., & Kim, J. W. (2008) · Archives of Pharmacal Research · doi:10.1007/s12272-001-1141-2 · Cited by 27
Increased oxidative stress in rats with chronic nitric oxide depletion:measurement of urinary 8-hydroxy-2′-deoxyguanosine excretion
Tsukahara, H., Hiraoka, M., Kobata, R., Hata, I., Ohshima, Y., Jiang, M., Noiri, E., & Mayumi, M. (2000) · Redox Report · doi:10.1179/rer.2000.5.1.23 · Cited by 27
The physiology ofS-nitrosothiols: carrier molecules for nitric oxide
Ng, E. S. M., & Kubes, P. (2003) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y03-078 · Cited by 27
Lecithinized superoxide dismutase reduces cold ischemia-induced chronic allograft dysfunction
Nakagawa, K., Koo, D. D. H., Davies, D. R., Gray, D. W. R., McLaren, A., Welsh, K. I., Morris, P. J., & Fuggle, S. V. (2002) · Kidney International · doi:10.1046/j.1523-1755.2002.00217.x · Cited by 26
Nitric oxide and the gut
Jourd’heuil, D., Grisham, M. B., & Granger, D. N. (1999) · Current Gastroenterology Reports · doi:10.1007/s11894-999-0019-1 · Cited by 25
Self-citation
Nitric oxide and prostacyclin pathways: An integrated mechanism that limits myocardial infarction progression in anaesthetized rats
Rossoni, G., Manfredi, B., DEGENNAROCOLONNA, V., Brini, A. T., Polvani, G., CLEMENT, M., & Berti, F. (2006) · Pharmacological Research · doi:10.1016/j.phrs.2006.01.004 · Cited by 25
Impact of ischemia/reperfusion injury and early inflammatory responses in kidney transplantation
Koo, D. D. H., & Fuggle, S. V. (2000) · Transplantation Reviews · doi:10.1053/trre.2000.16754 · Cited by 25
The impact of ischemic preconditioning on hemodynamic, biochemical and inflammatory alterations induced by intra-abdominal hypertension: an experimental study in a porcine model
Avraamidou, A., Marinis, A., Asonitis, S., Perrea, D. N., Polymeneas, G., Voros, D. C., & Αrgyra, E. (2012) · Langenbeck s Archives of Surgery · doi:10.1007/s00423-012-0977-x · Cited by 24
Montmorency cherry supplementation attenuates vascular dysfunction induced by prolonged forearm occlusion in overweight, middle-aged men
Bakkar, Z. A., Fulford, J., Gates, P. E., Jackman, S. R., JONES, A. M., Bond, B., & Bowtell, J. L. (2018) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00804.2018 · Cited by 27
The Effects of Oxidative Stress on the Liver and Ileum in Rats Caused by One-Lung Ventilation
Yuluğ, E., Tekinbaş, C., Ulusoy, H., Alver, A., Yeni̇lmez, E., Aydın, S., Çekiç, B., Topbaş, M., İmamoğlu, M., & Arvas, H. (2006) · Journal of Surgical Research · doi:10.1016/j.jss.2006.08.041 · Cited by 24
Effects of Dextran and Pentoxifylline on Hemorrhagic Shock-Induced P-Selectin Expression
Akgür, F. M., Zibari, G. B., McDonald, J. C., Granger, D. N., & Brown, M. F. (1999) · Journal of Surgical Research · doi:10.1006/jsre.1999.5758 · Cited by 24
Self-citation
Regulatory role of IKKɑ in myocardial ischemia/reperfusion injury by the determination of M1 versus M2 polarization of macrophages
Cao, Y., Xu, Y., Auchoybur, M. L., Chen, W., He, S., Qin, W., Su, C., Huang, F., Qiu, Z., Li, L., et al. (2018) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2018.08.021 · Cited by 23
Anti-inflammatory effect of thalidomide dithiocarbamate and dithioate analogs
Talaat, R. M., Elsayed, W., Agwa, H. S., Gamal‐Eldeen, A. M., Moawia, S., & Zahran, M. A. H. (2015) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2015.05.017 · Cited by 22
Protein nitration in cutaneous inflammation in the rat: essential role of inducible nitric oxide synthase and polymorphonuclear leukocytes
Greenacre, S. A. B., Rocha, F. A. C., Rawlingson, A., Meinerikandathevan, S., Poston, R. N., Ruiz, E., Halliwell, B. B., & Brain, S. D. (2002) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0704798 · Cited by 22
Insects as Sentinels of Oxidative Stress Induced by Environmental Contaminants: Biomarkers and Analytical Approaches
Messi, M., Giorgione, R., & Astolfi, M. L. (2025) · Toxics · doi:10.3390/toxics13080698 · Cited by 21
Effects of high glucose on NO synthesis in human keratinocyte cell line (HaCaT)
Nakai, K., Fujii, S., Yamamoto, A., Igarashi, J., Kubota, Y., & Kosaka, H. (2003) · Journal of Dermatological Science · doi:10.1016/s0923-1811(03)00006-9 · Cited by 21
Acetylsalicylic Acid Inhibits Monocyte Adhesion to Endothelial Cells by an Antioxidative Mechanism
Eisele, G., Schwedhelm, E., Schieffer, B., Tsikas, D., & Böger, R. H. (2004) · Journal of Cardiovascular Pharmacology · doi:10.1097/00005344-200404000-00006 · Cited by 21
Ischemia-reperfusion injury in rats affects hydraulic conductivity in two phases that are temporally and mechanistically separate
Victorino, G. P., Ramirez, R. M., Chong, T. J., Curran, B. C., & Sadjadi, J. (2008) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00419.2008 · Cited by 20
Ischemia–reperfusion injury: assessment and treatment, part II
McMichael, M. (2004) · Journal of Veterinary Emergency and Critical Care · doi:10.1111/j.1476-4431.2004.04005.x · Cited by 21
Divergent roles of superoxide and nitric oxide in liver ischemia and reperfusion injury
Hines, I. N., & Grisham, M. B. (2010) · Journal of Clinical Biochemistry and Nutrition · doi:10.3164/jcbn.11-016fr · Cited by 19
Self-citation
ROLE OF NITRIC OXIDE IN BIOLOGICAL SYSTEMS: A SYSTEMATIC REVIEW
Mirzaei, F., & Khazaei, M. (2017) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 19
Vasculoprotective Effects of Apolipoprotein Mimetic Peptides: An Evolving Paradigm in HDL Therapy
White, C. R., Datta, G., Mochon, P., Zhang, Z., Kelly, O., Curcio, C. A., Parks, D. A., Palgunachari, M. N., Handattu, S. P., Gupta, H., et al. (2009) · Vascular Disease Prevention · doi:10.2174/1567270000906010122 · Cited by 19
Inhibitory effects of eutigosides isolated fromEurya emarginata on the inflammatory mediators in RAW264.7 cells
Park, S. Y., Lee, H. J., Yoon, W., Kang, G. J., Moon, J. Y., Lee, N. H., Kim, S. J., Kang, H. K., & Yoo, E. S. (2005) · Archives of Pharmacal Research · doi:10.1007/bf02978207 · Cited by 19
Endothelin in the mechanism of endothelial injury and neutrophil adhesion in the post-ischemic guinea-pig heart
Kurzelewski, M., Czarnowska, E., & Berȩsewicz, A. (2002) · European Journal of Pharmacology · doi:10.1016/s0014-2999(01)01534-5 · Cited by 19
Myocardial Reperfusion Injury: Insights Gained from Gene-Targeted Mice
Jones, S. P., & Lefer, D. J. (2000) · Physiology · doi:10.1152/physiologyonline.2000.15.6.303 · Cited by 18
Self-citation
Superoxide activates very late antigen‐4 on an eosinophil cell line and increases cellular binding to vascular cell adhesion molecule‐1
Chuang, K., Tsai, W., Wang, Y., & Shieh, C. (2003) · European Journal of Immunology · doi:10.1002/eji.200323446 · Cited by 17
Coreolanceolins A–E, New Flavanones from the Flowers of Coreopsis lanceolate, and Their Antioxidant and Anti-Inflammatory Effects
Kim, H., Jung, Y. S., Oh, S. M., Oh, H., Ko, J., Kim, D., Kang, S. C., Lee, Y., Lee, D., & Baek, N. (2020) · Antioxidants · doi:10.3390/antiox9060539 · Cited by 16
Disposition of Protein-bound 3-nitrotyrosine in Rat Plasma Analysed by a Novel Protocol for HPLC-ECD
Hitomi, Y. H., Okuda, J., Nishino, H., Kambayashi, Y., Hibino, Y., Takemoto, K., Takigawa, T., Ohno, H., Taniguchi, N., & Ogino, K. (2007) · The Journal of Biochemistry · doi:10.1093/jb/mvm050 · Cited by 16
Oxidation of thiamine on reaction with nitrogen dioxide generated by ferric myoglobin and hemoglobin in the presence of nitrite and hydrogen peroxide
Stepuro, I. I., Oparin, A. Y., Stsiapura, V. I., Маскевич, С. А., & Titov, V. Y. (2012) · Biochemistry (Moscow) · doi:10.1134/s0006297912010051 · Cited by 17
Role of iron in ischemia-induced neurodegeneration: mechanisms and insights
Minhas, G., Modgil, S., & Anand, A. (2014) · Metabolic Brain Disease · doi:10.1007/s11011-014-9522-7 · Cited by 16
Involvement of NF-κB in the inhibitory actions of Platycarya strobilacea on the TNF-α-induced monocyte adhesion to colon epithelial cells and chemokine expression
Babu, D., Lee, J. S., Park, S., Thapa, D., Choi, M. K., Kim, A. R., Park, Y., & Kim, J. (2008) · Archives of Pharmacal Research · doi:10.1007/s12272-001-1219-0 · Cited by 16
Deletrious effect of prolonged cold ischemia on renal function
Stubenitsky, B. M., Brasile, L., Booster, M. H., Haisch, C. E., & Kootstra, G. (2001) · Transplant International · doi:10.1007/s001470100326 · Cited by 16
Quantitative determination of nitric oxide production in haemocytes: Nitrite reduction activity as a potential pathway of NO formation in haemolymph of Galleria mellonella larvae
Semenova, A. D., Glazachev, Y. I., Slepneva, I. A., & Glupov, V. V. (2014) · Nitric Oxide · doi:10.1016/j.niox.2013.12.011 · Cited by 16
Epidemiological and Pathogenic Relationship between Sleep Apnea and Ischemic Heart Disease
Carpio, C., Álvarez-Sala, R., & Rio, F. G. (2013) · Pulmonary Medicine · doi:10.1155/2013/405827 · Cited by 15
Serum nitrite and nitrate levels in children with obstructive sleep-disordered breathing
Kaditis, A. G., Alexopoulos, E. Ι., Ntamagka, G., Chaidas, K., Karathanasi, A., Gougoura, S. G., Papathanasiou, A. A., Liakos, P., Zintzaras, E., & Gourgoulianis, K. I. (2010) · Sleep Medicine · doi:10.1016/j.sleep.2009.03.013 · Cited by 15
Rac1 inhibition protects against hypoxia/reoxygenation-induced lipid peroxidation in human vascular endothelial cells
Martín, S. F., Chatterjee, S. B., Parinandi, N. L., & Alevriadou, B. R. (2005) · Vascular Pharmacology · doi:10.1016/j.vph.2005.05.002 · Cited by 15
Elevated circulating levels of soluble CD‐40 ligand in haemodialysis patients with symptomatic coronary heart disease
Lim, P.-S., Wu, M.-Y., Chien, S.-W., Wu, T.-K., LIU, C., HU, C., Chang, H., & Pai, M.-A. T. (2008) · Nephrology · doi:10.1111/j.1440-1797.2008.00999.x · Cited by 15
Nitric oxide-modulating biomaterials for therapeutic Immunoengineering
Boo, Y., Choi, S., Kim, J., & Kim, W. J. (2025) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2025.115718 · Cited by 16
RETRACTED: Multiple toxicity endpoints induced by carbon nanofibers in Amazon turtle juveniles: Outspreading warns about toxicological risks to reptiles
Guimarães, A. T. B., & Malafaia, G. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.146514 · Cited by 14
Retracted
GASTROINTESTINAL CIRCULATION
(1962) · Elsevier eBooks · doi:10.1016/b978-1-4832-3144-0.50015-1 · Cited by 14
RETRACTED: Carbon nanofibers are bioaccumulated in Aphylla williamsoni (Odonata) larvae and cause REDOX imbalance and changes of acetylcholinesterase activity
Montalvão, M. F., Guimarães, A. T. B., Rodrigues, A. S. D. L., & Malafaia, G. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.143991 · Cited by 13
Retracted
Chunghyuldan activates NOS mRNA expression and suppresses VCAM-1 mRNA expression in human endothelial cells
Park, S.-U., Jung, W., Moon, S., Ko, C., Cho, K., Kim, Y.-S., Bae, H.-S., & Chi, S.-G. (2005) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y05-106 · Cited by 13
The Role of TNF-Alpha in ALS: New Hypotheses for Future Therapeutic Approaches
Cereda, C., Gagliardi, S., Cova, E., Diamanti, L., & Ceroni, M. (2012) · InTech eBooks · doi:10.5772/31223 · Cited by 14
Effects of l-NA and Sodium Nitroprusside on Ischemia/Reperfusion-Induced Leukocyte Adhesion and Macromolecular Leakage in Hamster Cheek Pouch Venules
Simões-Gurgel, C., Svensjö, E., & Bouskela, E. (2001) · Microvascular Research · doi:10.1006/mvre.2001.2324 · Cited by 13
Sleep Apnea and Cardiovascular Diseases
Álvarez-Sala, R., Rio, F. G., del Campo, F., Zamarrón, C., & Netzer, N. C. (2014) · Pulmonary Medicine · doi:10.1155/2014/690273 · Cited by 13
Cardioplegia and Surgical Ischemia
Chambers, D. J., & Hearse, D. J. (2001) · Elsevier eBooks · doi:10.1016/b978-012656975-9/50053-5 · Cited by 13
Concentration decrease of nitric oxide in the postischemic muscle is not only caused by the generation of O
Stoffels, F., Lohöfener, F., Beissenhirtz, M. K., Lisdat, F., & Büttemeyer, R. (2007) · Microsurgery · doi:10.1002/micr.20403 · Cited by 12
Blocking leukocyte influx and function to prevent chronic lung disease of prematurity
Auten, R. L., & Ekekezie, I. I. (2003) · Pediatric Pulmonology · doi:10.1002/ppul.10275 · Cited by 12
A radical approach to treating inflammation
Grisham, M. B. (2000) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(99)01435-2 · Cited by 12
Self-citation
Long-term exposure of zebrafish juveniles to carbon nanofibers at predicted environmentally relevant concentrations: Outspreading warns about ecotoxicological risks to freshwater fish
Montalvão, M. F., Chagas, T. Q., Rodrigues, A. S. D. L., Guimarães, A. T. B., & Malafaia, G. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.163153 · Cited by 11

Authors: Grisham, M. B., Granger, D. N., & Lefer, D. J.
Affiliations: Louisiana State University (US)
Corresponding author: Grisham, Matthew B.
ORCID: Grisham, Matthew B.
Lefer, David J.
Venue: Free Radical Biology and Medicine
Publisher: Elsevier BV
Published: 1998-09
Volume: 25
Issue: 4-5
Pages: 404-433
ISSN: 0891-5849 (ISSN-L)
DOI: 10.1016/s0891-5849(98)00094-x
OpenAlex: W2094525668
Cited by: 293
References: 211
Citations by year: 2025: 5 · 2024: 5 · 2023: 4 · 2022: 4 · 2021: 4 · 2020: 11 · 2019: 5 · 2018: 4 · 2017: 4 · 2016: 4 · 2015: 6 · 2014: 7 · 2013: 6 · 2012: 11
FWCI: 3.21
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
Locations: Free Radical Biology and Medicine (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health (5r01dk047663-06)
National Institute of Diabetes and Digestive and Kidney Diseases (P01 DK-43785, DK-47663, P01DK043785)
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: reactive oxygen species, reactive nitrogen species, leukocyte-endothelium interaction, ischemia-reperfusion injury, ischemic heart disease, nitric oxide donors, leukocyte adhesion, transendothelial migration, platelet aggregation, microvascular damage, oxidative stress
MeSH terms: Animals, Cell Adhesion, Endothelium, Vascular, Humans, Iron, Leukocytes, Nitric Oxide, Oxidation-Reduction, Myocardial Reperfusion Injury, Myocardial Ischemia, Reactive Oxygen Species

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

Modulation of leukocyte–endothelial interactions by reactive metabolites of oxygen and nitrogen: relevance to ischemic heart disease

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks