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. 2013 Sep 24;2013:985210. doi: 10.1155/2013/985210

Table 1.

Effects of different antioxidant treatments in β thalassemia.

Molecule Model Evidences Ref.
Vitamin E β-thal intermedia patients (in vivo study) ↓ MDA
Amelioration in the oxidation of low density lipoproteins
Amelioration of RBCs osmotic fragility
No changes in transfusion requirement
[7072]
Curcumin β-thal patients
(in vitro study) 
β-thal/HbE patients
(in vivo study)
↓ lipid peroxidation
↓ methemoglobin, but no changes in Hb levels
[73, 74]
FPP β-thal major and intermedia patients
(in vitro study) 
β-thal/HbE patients
(in vivo study) 
β-thal mouse model
(in vivo)
↓ ROS
↑ GSH
↓ PS positive RBCs
↓ RBCs phagocytosis
No effects on Hb levels
[73, 75]
MonoHER β-thal mouse model
(in vivo)
↑ RBCs K+ content
↓ KCl cotransport activity
↓ PS positive RBCs
↑ RBCs membrane and plasma vitamin E levels
Amelioration of β-thal mouse erythropoiesis
[66]
AD4 β-thal major and intermedia patients
(in vitro study) 
β-thal mouse model
(in vivo study)
↓ ROS
↑ GSH
↓ PS positive RBCs
↓ RBCs phagocytosis
No effects on Hb levels
[76]

β-thal: β-thalassemia; MDA: malonylaldehyde; RBC: red blood cell; Hb: hemoglobin; PS: phosphatidylserine; GSH: reduced glutathione peroxidase; ROS: reactive oxygen species; FPP: fermented papaya preparation; AD4: N-acetylcysteine amide.