Scopul nostru este sprijinirea şi promovarea cercetării ştiinţifice şi facilitarea comunicării între cercetătorii români din întreaga lume.
Autori: F. Safciuc, A. Constantin, A. Manea, M. Nicolae, D. Popov, M. Raicu, D. Alexandru, E. Constantinescu
Editorial: Bentham Sci Publishers Ltd., Current Neurovascular Research, 4, p.228-234, 2007.
Biological aging is associated with an increased incidence of cerebrovascular disease. Recent findings indicate that oxidative stress promoting age-related changes of cerebral circulation are involved in neurodegenerative disorders such as Alzheimer’s disease(AD) and Parkinson’s disease. The aim of this study was to evaluate the contribution of cerebral microvessels to the oxidative stress during brain aging, by: (i) assessment of precursors for advanced glycation end products (AGE) formation, (ii) activities of antioxidant enzymes,namely superoxide dismutase (SOD), glutathione peroxidase (GPx) and glutathione disulfide reductase (GR), and (iii) the activities
of metalloproteinases (MMPs), MMP-2 and MMP-9, involved in synaptogenesis and memory consolidation. The experiments were performed on two groups of male Wistar rats: 15 young (3-6 months old) and 15 aged (18-24 months old) animals. The cerebral microvessels were isolated by mechanical homogenization, the concentration of protein carbonyls and the activity of antioxidant enzymes
were evaluated by spectrophotometry, and gelatin SDS-PAGE zymography was employed to evaluate MMP-2 and MMP-9 activities. The results showed that, by comparison with young rats, aged brain microvessels contain: (i) ~ 106 % increase of protein carbonyls production;(ii) ~ 68% higher GPx activity, unmodified activities of SOD and GR; (iii) ~ 30% diminishment in MMP-2 activity, and the specific
occurrence of MMP-9 enzyme. The data suggest that the age-related changes of microvessels could increase the propensity for cerebral diseases and might represent, at least in part, a prerequisite for the deterioration of mental and physical status in the elderly.
Cuvinte cheie: imbatranirea creierului, microvasculatura, stres oxidativ, carbonili proteici, enzime antioxidante, metaloproteinaze // brain aging, microvessels, oxidative stress, protein carbonyls, antioxidant enzymes, metalloproteinases