Open AccessAge-Related Defects in Erythrocyte 2,3-Diphosphoglycerate Metabolism in Dementia
Author(s) -
Yury G. Kaminsky,
V. Prakash Reddy,
Ghulam Md Ashraf,
Ausaf Ahmad,
Valery V. Benberin,
Elena Kosenko,
Gjumrakch Aliev
Publication year - 2013
Publication title -
aging and disease
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.808
H-Index - 54
ISSN - 2152-5250
DOI - 10.14336/ad.2013.0400244
Subject(s) - glycolysis , phosphofructokinase , hexokinase , dementia , pathogenesis , medicine , alzheimer's disease , endocrinology , enzyme , metabolism , disease , diphosphoglycerate , phosphoglycerate mutase , biochemistry , biology , hemoglobin
Alzheimer disease (AD) is the most common dementing illness. Metabolic defects in the brain with aging contribute to the pathogenesis of AD. These changes can be found systematically and thus can be used as potential biomarkers. Erythrocytes (RBCs) are passive "reporter cells" that are not well studied in AD. In the present study, we analyzed an array of glycolytic and related enzymes and intermediates in RBCs from patients with AD and non-Alzheimer dementia (NA), age-matched controls (AC) and young adult controls (YC). AD is characterized by higher activities of hexokinase, phosphofructokinase, and bisphosphoglycerate mutase and bisphosphoglycerate phosphatase in RBCs. In our study, we observed that glycolytic and related enzymes displayed significantly lower activities in AC. However, similar or significantly higher activities were observed in AD and NA groups as compared to YC group. 2,3-diphosphoglycerate (2,3-DPG) levels were significantly decreased in AD and NA patients. The pattern of changes between groups in the above indices strongly correlates with each other. Collectively, our data suggested that AD and NA patients are associated with chronic disturbance of 2,3-DPG metabolism in RBCs. These defects may play a pivotal role in physiological processes, which predispose elderly subjects to AD and NA.