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deferoxamine and Coronary Disease

deferoxamine has been researched along with Coronary Disease in 24 studies

Deferoxamine: Natural product isolated from Streptomyces pilosus. It forms iron complexes and is used as a chelating agent, particularly in the mesylate form.
desferrioxamine B : An acyclic desferrioxamine that is butanedioic acid in which one of the carboxy groups undergoes formal condensation with the primary amino group of N-(5-aminopentyl)-N-hydroxyacetamide and the second carboxy group undergoes formal condensation with the hydroxyamino group of N(1)-(5-aminopentyl)-N(1)-hydroxy-N(4)-[5-(hydroxyamino)pentyl]butanediamide. It is a siderophore native to Streptomyces pilosus biosynthesised by the DesABCD enzyme cluster as a high affinity Fe(III) chelator.

Coronary Disease: An imbalance between myocardial functional requirements and the capacity of the CORONARY VESSELS to supply sufficient blood flow. It is a form of MYOCARDIAL ISCHEMIA (insufficient blood supply to the heart muscle) caused by a decreased capacity of the coronary vessels.

Research Excerpts

ExcerptRelevanceReference
"Salicylic acid was used as the probe for ."1.28Quantification of hydroxyl radical and its lack of relevance to myocardial injury during early reperfusion after graded ischemia in rat hearts. ( Ashraf, M; Onodera, T; Takemura, G, 1992)
"Deferoxamine pretreatment also decreased (P less than ."1.28Deferoxamine pretreatment reduces canine infarct size and oxidative injury. ( Horwitz, LD; Lesnefsky, EJ; Repine, JE, 1990)
"Deferoxamine-treated hearts recovered 99 +/- 10% of control PCr content, while untreated hearts recovered 60 +/- 16% (p less than ."1.27Improvement of postischemic myocardial function and metabolism induced by administration of deferoxamine at the time of reflow: the role of iron in the pathogenesis of reperfusion injury. ( Ambrosio, G; Flaherty, JT; Jacobus, WE; Weisfeldt, ML; Zweier, JL, 1987)

Research

Studies (24)

TimeframeStudies, this research(%)All Research%
pre-199014 (58.33)18.7374
1990's8 (33.33)18.2507
2000's2 (8.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Patterson, E1
Duffy, SJ1
Biegelsen, ES1
Holbrook, M1
Russell, JD1
Gokce, N1
Keaney, JF1
Vita, JA1
Chekanov, VS1
Nikolaychik, V1
Boucher, F1
Pucheu, S1
Coudray, C1
Favier, A1
de Leiris, J1
Takemura, G1
Onodera, T1
Ashraf, M1
Mousa, SA1
Ritger, RC1
Smith, RD1
McCord, JM2
Liu, XK1
Prasad, MR1
Engelman, RM1
Jones, RM1
Das, DK1
van Jaarsveld, H2
Potgieter, GM2
Barnard, SP2
Potgieter, S1
Lesnefsky, EJ1
Repine, JE1
Horwitz, LD1
Maxwell, MP1
Hearse, DJ2
Yellon, DM1
Sullivan, JL2
Ambrosio, G1
Zweier, JL1
Jacobus, WE1
Weisfeldt, ML1
Flaherty, JT1
Bernard, M1
Menasché, P2
Piétri, S1
Grousset, C2
Piwnica, A2
Cozzone, PJ1
Groenewald, AJ1
Vermaak, WJ1
Barnard, HC1
Russell, WJ1
Bernier, M1
Manning, AS1
Gauduel, Y1
Mouas, C1
Bolli, R1
Patel, BS1
Zhu, WX1
O'Neill, PG1
Hartley, CJ1
Charlat, ML1
Roberts, R1
Badylak, SF1
Simmons, A1
Turek, J1
Babbs, CF1
Boffa, GM1
Ferrari, R1
Dalla Volta, S1
Myers, CL2
Weiss, SJ2
Kirsh, MM2
Shepard, BM1
Shlafer, M2

Reviews

1 review available for deferoxamine and Coronary Disease

ArticleYear
The iron paradigm of ischemic heart disease.
    American heart journal, 1989, Volume: 117, Issue:5

    Topics: Animals; Coronary Disease; Deferoxamine; Female; Humans; Iron; Male; Menopause; Models, Cardiovascul

1989

Trials

1 trial available for deferoxamine and Coronary Disease

ArticleYear
Iron chelation improves endothelial function in patients with coronary artery disease.
    Circulation, 2001, Jun-12, Volume: 103, Issue:23

    Topics: Adult; Blood Flow Velocity; Coronary Disease; Deferoxamine; Endothelium, Vascular; Enzyme Inhibitors

2001

Other Studies

22 other studies available for deferoxamine and Coronary Disease

ArticleYear
Coronary vascular injury following transient coronary artery occlusion: prevention by pretreatment with deferoxamine, dimethylthiourea and N-2-mercaptoproprionyl glycine.
    The Journal of pharmacology and experimental therapeutics, 1993, Volume: 266, Issue:3

    Topics: Animals; Capillary Permeability; Coronary Disease; Coronary Vessels; Deferoxamine; Dogs; Lipid Perox

1993
Iron contributes to endothelial dysfunction in acute ischemic syndromes.
    Circulation, 2002, Jan-29, Volume: 105, Issue:4

    Topics: Acute Disease; Coronary Circulation; Coronary Disease; Deferoxamine; Endothelial Growth Factors; End

2002
Evidence of cytosolic iron release during post-ischaemic reperfusion of isolated rat hearts. Influence on spin-trapping experiments with DMPO.
    FEBS letters, 1992, May-18, Volume: 302, Issue:3

    Topics: Animals; Coronary Disease; Cyclic N-Oxides; Cytosol; Deferoxamine; Electron Spin Resonance Spectrosc

1992
Quantification of hydroxyl radical and its lack of relevance to myocardial injury during early reperfusion after graded ischemia in rat hearts.
    Circulation research, 1992, Volume: 71, Issue:1

    Topics: Animals; Coronary Disease; Deferoxamine; Free Radicals; Gentisates; Heart; Hydroxides; Hydroxybenzoa

1992
Efficacy and safety of deferoxamine conjugated to hydroxyethyl starch.
    Journal of cardiovascular pharmacology, 1992, Volume: 19, Issue:3

    Topics: Animals; Coronary Disease; Deferoxamine; Edema; Hemodynamics; Hydroxyethyl Starch Derivatives; Lipid

1992
Is iron sufficiency a risk factor in ischemic heart disease?
    Circulation, 1991, Volume: 83, Issue:3

    Topics: Coronary Disease; Deferoxamine; Free Radicals; Humans; Iron; Myocardial Reperfusion Injury; Oxygen;

1991
Role of iron on membrane phospholipid breakdown in ischemic-reperfused rat heart.
    The American journal of physiology, 1990, Volume: 259, Issue:4 Pt 2

    Topics: Acylation; Animals; Coronary Disease; Deferoxamine; Fatty Acids, Nonesterified; Heart; Heart Ventric

1990
Improvement of ischemic and postischemic mitochondrial function by deferrioxamine: the role of iron.
    Advances in experimental medicine and biology, 1990, Volume: 264

    Topics: Animals; Coronary Disease; Cytosol; Deferoxamine; In Vitro Techniques; Iron; Male; Mitochondria, Hea

1990
Deferoxamine pretreatment reduces canine infarct size and oxidative injury.
    The Journal of pharmacology and experimental therapeutics, 1990, Volume: 253, Issue:3

    Topics: Animals; Coronary Disease; Coronary Vessels; Deferoxamine; Dogs; Glutathione; Hemodynamics; Male; My

1990
Inability of desferrioxamine to limit tissue injury in the ischaemic and reperfused rabbit heart.
    Journal of cardiovascular pharmacology, 1989, Volume: 13, Issue:4

    Topics: Animals; Coronary Disease; Deferoxamine; Free Radicals; Hemodynamics; Hydroxides; Hydroxyl Radical;

1989
Improvement of postischemic myocardial function and metabolism induced by administration of deferoxamine at the time of reflow: the role of iron in the pathogenesis of reperfusion injury.
    Circulation, 1987, Volume: 76, Issue:4

    Topics: Adenosine Triphosphate; Animals; Coronary Circulation; Coronary Disease; Deferoxamine; Electron Spin

1987
Cardioplegic arrest superimposed on evolving myocardial ischemia. Improved recovery after inhibition of hydroxyl radical generation by peroxidase or deferoxamine. A 31P nuclear resonance study.
    Circulation, 1988, Volume: 78, Issue:5 Pt 2

    Topics: Animals; Coronary Disease; Deferoxamine; Heart Arrest, Induced; Hydrogen-Ion Concentration; Hydroxid

1988
The effect of allopurinol and deferrioxamine on rat heart mitochondrial oxidative phosphorylation after normothermic ischemic cardiac arrest and of reperfusion.
    Research communications in chemical pathology and pharmacology, 1988, Volume: 62, Issue:3

    Topics: Adenosine Diphosphate; Allopurinol; Animals; Coronary Disease; Deferoxamine; Heart Arrest; In Vitro

1988
Inactivation of creatine phosphokinase by superoxide during reperfusion injury.
    Basic life sciences, 1988, Volume: 49

    Topics: Animals; Catalase; Cattle; Coronary Disease; Creatine Kinase; Deferoxamine; Disease Models, Animal;

1988
Sex, iron, and heart disease.
    Lancet (London, England), 1986, Nov-15, Volume: 2, Issue:8516

    Topics: Coronary Disease; Deferoxamine; Female; Humans; Iron Deficiencies; Male; Sex Factors

1986
Reperfusion-induced arrhythmias and oxygen-derived free radicals. Studies with "anti-free radical" interventions and a free radical-generating system in the isolated perfused rat heart.
    Circulation research, 1986, Volume: 58, Issue:3

    Topics: Animals; Arrhythmias, Cardiac; Catalase; Coronary Circulation; Coronary Disease; Deferoxamine; Free

1986
[A new concept of cardioplegic protection in cardiac surgery: iron chelation].
    Archives des maladies du coeur et des vaisseaux, 1988, Volume: 81, Issue:6

    Topics: Animals; Cardiac Surgical Procedures; Cardioplegic Solutions; Coronary Disease; Deferoxamine; Extrac

1988
The iron chelator desferrioxamine attenuates postischemic ventricular dysfunction.
    The American journal of physiology, 1987, Volume: 253, Issue:6 Pt 2

    Topics: Animals; Arrhythmias, Cardiac; Coronary Circulation; Coronary Disease; Coronary Vessels; Deferoxamin

1987
Protection from reperfusion injury in the isolated rat heart by postischaemic deferoxamine and oxypurinol administration.
    Cardiovascular research, 1987, Volume: 21, Issue:7

    Topics: Animals; Coronary Disease; Creatine Kinase; Deferoxamine; Heart; Male; Microscopy, Electron; Myocard

1987
[Prevention of myocardial damage by oxygen free radicals. Theoretical premises and experimental data].
    Cardiologia (Rome, Italy), 1985, Volume: 30, Issue:10

    Topics: Allopurinol; Animals; Antioxidants; Coronary Disease; Deferoxamine; Dogs; Free Radicals; Iron; Manni

1985
Effects of supplementing hypothermic crystalloid cardioplegic solution with catalase, superoxide dismutase, allopurinol, or deferoxamine on functional recovery of globally ischemic and reperfused isolated hearts.
    The Journal of thoracic and cardiovascular surgery, 1986, Volume: 91, Issue:2

    Topics: Allopurinol; Animals; Bicarbonates; Blood Pressure; Calcium Chloride; Catalase; Coronary Circulation

1986
Involvement of hydrogen peroxide and hydroxyl radical in the 'oxygen paradox': reduction of creatine kinase release by catalase, allopurinol or deferoxamine, but not by superoxide dismutase.
    Journal of molecular and cellular cardiology, 1985, Volume: 17, Issue:7

    Topics: Allopurinol; Animals; Blood Pressure; Catalase; Coronary Circulation; Coronary Disease; Creatine Kin

1985