Glutathione Redox System in β-Thalassemia/Hb E Patients

β-thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects animal cells from oxidative damage. This study aimed to determine the effect of disease state and splenectomy on redox status expressed by whole bl...

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Published inTheScientificWorld Vol. 2013; no. 2013; pp. 1 - 7
Main Authors Siritanaratkul, Noppadol, Panichkul, Narumol, Charoensakdi, Ratiya, Hatairaktham, Suneerat, Tangjaidee, Thongchai, Kalpravidh, Ruchaneekorn W., Fucharoen, Suthat
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Published Cairo, Egypt Hindawi Publishing Corporation 01.01.2013
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Abstract β-thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects animal cells from oxidative damage. This study aimed to determine the effect of disease state and splenectomy on redox status expressed by whole blood glutathione (GSH)/glutathione disulfide (GSSG) and also to evaluate glutathione-related responses to oxidation in β-thalassemia/Hb E patients. Twenty-seven normal subjects and 25 β-thalassemia/Hb E patients were recruited and blood was collected. The GSH/GSSG ratio, activities of glutathione-related enzymes, hematological parameters, and serum ferritin levels were determined in individuals. Patients had high iron-induced oxidative stress, shown as significantly increased serum ferritin, a decreased GSH/GSSG ratio, and increased activities of glutathione-related enzymes. Splenectomy increased serum ferritin levels and decreased GSH levels concomitant with unchanged glutathione-related enzyme activities. The redox ratio had a positive correlation with hemoglobin levels and negative correlation with levels of serum ferritin. The glutathione system may be the body’s first-line defense used against oxidative stress and to maintain redox homeostasis in thalassemic patients based on the significant correlations between the GSH/GSSH ratio and degree of anemia or body iron stores.
AbstractList β-thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects animal cells from oxidative damage. This study aimed to determine the effect of disease state and splenectomy on redox status expressed by whole blood glutathione (GSH)/glutathione disulfide (GSSG) and also to evaluate glutathione-related responses to oxidation in β-thalassemia/Hb E patients. Twenty-seven normal subjects and 25 β-thalassemia/Hb E patients were recruited and blood was collected. The GSH/GSSG ratio, activities of glutathione-related enzymes, hematological parameters, and serum ferritin levels were determined in individuals. Patients had high iron-induced oxidative stress, shown as significantly increased serum ferritin, a decreased GSH/GSSG ratio, and increased activities of glutathione-related enzymes. Splenectomy increased serum ferritin levels and decreased GSH levels concomitant with unchanged glutathione-related enzyme activities. The redox ratio had a positive correlation with hemoglobin levels and negative correlation with levels of serum ferritin. The glutathione system may be the body’s first-line defense used against oxidative stress and to maintain redox homeostasis in thalassemic patients based on the significant correlations between the GSH/GSSH ratio and degree of anemia or body iron stores.
β -thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects animal cells from oxidative damage. This study aimed to determine the effect of disease state and splenectomy on redox status expressed by whole blood glutathione (GSH)/glutathione disulfide (GSSG) and also to evaluate glutathione-related responses to oxidation in β -thalassemia/Hb E patients. Twenty-seven normal subjects and 25 β -thalassemia/Hb E patients were recruited and blood was collected. The GSH/GSSG ratio, activities of glutathione-related enzymes, hematological parameters, and serum ferritin levels were determined in individuals. Patients had high iron-induced oxidative stress, shown as significantly increased serum ferritin, a decreased GSH/GSSG ratio, and increased activities of glutathione-related enzymes. Splenectomy increased serum ferritin levels and decreased GSH levels concomitant with unchanged glutathione-related enzyme activities. The redox ratio had a positive correlation with hemoglobin levels and negative correlation with levels of serum ferritin. The glutathione system may be the body's first-line defense used against oxidative stress and to maintain redox homeostasis in thalassemic patients based on the significant correlations between the GSH/GSSH ratio and degree of anemia or body iron stores.β -thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects animal cells from oxidative damage. This study aimed to determine the effect of disease state and splenectomy on redox status expressed by whole blood glutathione (GSH)/glutathione disulfide (GSSG) and also to evaluate glutathione-related responses to oxidation in β -thalassemia/Hb E patients. Twenty-seven normal subjects and 25 β -thalassemia/Hb E patients were recruited and blood was collected. The GSH/GSSG ratio, activities of glutathione-related enzymes, hematological parameters, and serum ferritin levels were determined in individuals. Patients had high iron-induced oxidative stress, shown as significantly increased serum ferritin, a decreased GSH/GSSG ratio, and increased activities of glutathione-related enzymes. Splenectomy increased serum ferritin levels and decreased GSH levels concomitant with unchanged glutathione-related enzyme activities. The redox ratio had a positive correlation with hemoglobin levels and negative correlation with levels of serum ferritin. The glutathione system may be the body's first-line defense used against oxidative stress and to maintain redox homeostasis in thalassemic patients based on the significant correlations between the GSH/GSSH ratio and degree of anemia or body iron stores.
β ‐thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects animal cells from oxidative damage. This study aimed to determine the effect of disease state and splenectomy on redox status expressed by whole blood glutathione (GSH)/glutathione disulfide (GSSG) and also to evaluate glutathione‐related responses to oxidation in β ‐thalassemia/Hb E patients. Twenty‐seven normal subjects and 25 β ‐thalassemia/Hb E patients were recruited and blood was collected. The GSH/GSSG ratio, activities of glutathione‐related enzymes, hematological parameters, and serum ferritin levels were determined in individuals. Patients had high iron‐induced oxidative stress, shown as significantly increased serum ferritin, a decreased GSH/GSSG ratio, and increased activities of glutathione‐related enzymes. Splenectomy increased serum ferritin levels and decreased GSH levels concomitant with unchanged glutathione‐related enzyme activities. The redox ratio had a positive correlation with hemoglobin levels and negative correlation with levels of serum ferritin. The glutathione system may be the body’s first‐line defense used against oxidative stress and to maintain redox homeostasis in thalassemic patients based on the significant correlations between the GSH/GSSH ratio and degree of anemia or body iron stores.
Audience Academic
Author Fucharoen, Suthat
Siritanaratkul, Noppadol
Charoensakdi, Ratiya
Hatairaktham, Suneerat
Tangjaidee, Thongchai
Panichkul, Narumol
Kalpravidh, Ruchaneekorn W.
AuthorAffiliation 3 Thalassemia Research Center, Institute of Molecular Biosciences, Mahidol University, Nakhon Pathom 73170, Thailand
1 Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand
2 Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand
AuthorAffiliation_xml – name: 1 Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand
– name: 3 Thalassemia Research Center, Institute of Molecular Biosciences, Mahidol University, Nakhon Pathom 73170, Thailand
– name: 2 Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/24223032$$D View this record in MEDLINE/PubMed
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Copyright © 2013 Ruchaneekorn W. Kalpravidh et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0
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18082636 - Biochim Biophys Acta. 2008 Feb;1780(2):249-55
17010049 - Br J Haematol. 2006 Oct;135(2):254-63
21712504 - Toxicol Sci. 2011 Sep;123(1):58-70
21647434 - PLoS One. 2011;6(5):e20151
9105255 - Clin Chem. 1997 Apr;43(4):562-8
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Snippet β-thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects animal...
β ‐thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects...
β -thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects...
β -thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects...
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StartPage 1
SubjectTerms Acids
Anemia
Antioxidants
beta-Thalassemia - blood
beta-Thalassemia - metabolism
beta-Thalassemia - surgery
Biochemistry
Blood
Case-Control Studies
Correlation
Enzymatic activity
Enzymes
Female
Ferritin
Ferritins - blood
Glutathione
Glutathione - blood
Glutathione Disulfide - blood
Health aspects
Hematology
Hemoglobin
Hemoglobin E - analysis
Homeostasis
Humans
Iron
Male
Oxidation
Oxidation-Reduction
Oxidation-reduction reaction
Oxidative stress
Patients
Physiological aspects
Protein research
Sensors
Splenectomy
Thalassemia
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Title Glutathione Redox System in β-Thalassemia/Hb E Patients
URI https://search.emarefa.net/detail/BIM-1033046
https://dx.doi.org/10.1155/2013/543973
https://www.ncbi.nlm.nih.gov/pubmed/24223032
https://www.proquest.com/docview/2175222426
https://www.proquest.com/docview/1458502495
https://pubmed.ncbi.nlm.nih.gov/PMC3816076
https://doaj.org/article/0c6656f676344c118cffe4be7f872a80
Volume 2013
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