MAO inhibitors and oxidant stress in aging brain tissue

Citation
G. Alper et al., MAO inhibitors and oxidant stress in aging brain tissue, EUR NEUROPS, 9(3), 1999, pp. 247-252
Citations number
32
Categorie Soggetti
Neurosciences & Behavoir
Journal title
EUROPEAN NEUROPSYCHOPHARMACOLOGY
ISSN journal
0924977X → ACNP
Volume
9
Issue
3
Year of publication
1999
Pages
247 - 252
Database
ISI
SICI code
0924-977X(199903)9:3<247:MIAOSI>2.0.ZU;2-W
Abstract
The process of aging presents itself with various alterations in physiologi cal events. Among many theories, the free radical (FR) theory of aging whic h reflects the FR damage to cellular components is accepted as one of the m ost important theories. Recently, the increases in catecholamine metabolism in aging have also attracted attention, and monoamine oxidase (MAO), a key enzyme in this process has been extensively studied. The aim of this study was to assess the role of FR species via MAO, a possible source of FRs, in physiological aging by determining the lipid peroxidation products (LPP) ( malondialdehyde, diene conjugates) and antioxidant enzyme levels (superoxid e dismutase (SOD) and catalase (CAT) in young (3 months old, n=10) and agin g (16-18 months old, n=10) rat brain tissues of Swiss male albino rats. In the second part of the study, the same parameters were determined after the acute administration of MAO inhibitors (deprenyl and pargyline, 25 mg/kg i .p.) to investigate whether these agents have any beneficial effects in red ucing oxidant stress via inhibition of MAO. In old rat brains, MAO activiti es showed a significant increase (P=0.000) in addition to an insignificant increase in LPP, while SOD (P=0.007) and CAT activities showed a decrease w ith advancing age. After the acute administration of both deprenyl and parg yline, a significant decrease in the MAO activities of both young (P=0.0002 for each) and aging rats (P=0.0002 for deprenyl and P=0.0001 for pargyline ) were observed. It was noted that deprenyl causes a significant increase i n CAT activity (P<0.05) but a significant decrease in SOD activity (P<0.05) in young rats, while it causes only a significant increase in SOD activity in aging rats (P<0.05). Both deprenyl and pargyline cause a significant de crease in conjugated diene levels of aging rats (P<0.05). These results con firm the role of catecholamine oxidation and MAO activity as one of the cau sative factors in increased oxidant stress during aging. By reducing the ox idant stress observed in aging brain, MAO inhibitors, especially deprenyl, may contribute to the control of the aging process. (C) 1999 Elsevier Scien ce B.V. All rights reserved.