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Antioxidants in erythrocytes in aging and dementia
Author(s) -
Еlena Kosenko,
Lyudmila Tikhonova,
Armenuhi C. Poghosyan,
Y. G. Kaminsky
Publication year - 2013
Publication title -
biomeditsinskaya khimiya
Language(s) - English
Resource type - Journals
eISSN - 2310-6972
pISSN - 2310-6905
DOI - 10.18097/pbmc20135904443
Subject(s) - glutathione , glutathione peroxidase , oxidative stress , glutathione reductase , antioxidant , superoxide dismutase , glutathione disulfide , chemistry , medicine , endocrinology , biochemistry , alzheimer's disease , ageing , catalase , biology , enzyme , disease
Age of patients and brain oxidative stress may contribute to pathogenesis of Alzheimer's disease (AD). Erythrocytes (red blood cells, RBC) are considered as passive "reporter cells" for the oxidative status of the whole organism and are not well studied in AD. The aim of this work was to assess whether the antioxidant status of RBC changes in aging and AD. Blood was taken from AD and non-Alzheimer's dementia patients, aged-matched and younger controls. In vivo antioxidant status was assessed in each of the study subjects by measuring RBC levels of H202, organic hydroperoxides, glutathione (GSH) and glutathione disulfide (GSSG), activities of superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase, glutathione S-transferase, and glucose-6-phosphate dehydrogenase. In both aging and dementia, oxidative stress in RBC was shown to increase and to be expressed in elevated concentrations of H202 and organic hydroperoxides, decreased the GSH/GSSG ratio and glutathione S-transferase activity. Decreased glutathione peroxidase activity in RBC may be considered as a new peripheral marker for Alzheimer's disease while alterations of other parameters of oxidative stress reflect age-related events.

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