L1 effects on reactive oxygen (ROS) and nitrogen species (RNS) release, hemoglobin oxidation, low molecular weight antioxidants, and antioxidant enzyme activities in red and white blood cells of thalassemic patients

Transfusion Science

Volumn 23, Issue 3, 2000, Pages 253-254

  Korkina, L ^a   De Luca, C ^b   Deeva, I ^a   Perrotta, S ^c   Nobili, B ^c   Passi, S ^b   Puddu, P ^c  

^a PIROGOV RUSSIAN NATIONAL RESEARCH MEDICAL UNIVERSITY   (Russian Federation)

^b LABORATORIO DI PATOLOGIA VASCOLARE   (Italy)

^c SECOND UNIVERSITY OF NAPLES   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIOXIDANT; CATALASE; DEFERIPRONE; DEFEROXAMINE MESYLATE; GLUTATHIONE; GLUTATHIONE PEROXIDASE; GLUTATHIONE TRANSFERASE; HEMOGLOBIN; HYDROXYL RADICAL; IRON; METHEMOGLOBIN; NITROGEN; PEROXYNITRITE; REACTIVE OXYGEN METABOLITE; SUPEROXIDE; SUPEROXIDE DISMUTASE; TOCOPHEROL; UBIDECARENONE;

BETA THALASSEMIA; BLOOD TRANSFUSION; CONFERENCE PAPER; ENZYME ACTIVITY; ERYTHROCYTE; HUMAN; HUMAN CELL; IRON CHELATION; IRON OVERLOAD; LEUKOCYTE; OXIDATIVE STRESS;

ANTIOXIDANTS; BETA-THALASSEMIA; DEFEROXAMINE; ERYTHROCYTES; HEMOGLOBINS; HUMANS; IRON CHELATING AGENTS; LEUKOCYTES; OXIDATION-REDUCTION; OXYGEN; PYRIDONES;

EID: 0033694227     PISSN: 09553886     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0955-3886(00)00099-0     Document Type: Conference Paper

References (4)

1. Oxidative denaturation of red blood cells in thalassemia
2. Oxidative stress and antioxidant status in β-thalassemia major: Iron overload and depletion of lipid soluble antioxidants
3. Hydroxyl radical generation in beta-thalassemic red blood cells
4. Blood antioxidant status and urinary levels of catecholamine metabolites in β-thalassemia