Loss of adaptation to oxidative stress as a mechanism for aortic damage in aging rats

Cells are armed with a vast repertoire of antioxidant defence mechanisms to prevent the accumulation of oxidative damage. The cellular adaptive response is an important antioxidant mechanism against physiological and pathophysiological oxidative alterations in a cell's microenvironment. The aim...

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Bibliographic Details
Published in:Journal of physiology and biochemistry 2007-09, Vol.63 (3), p.239-247
Main Authors: Mármol, F, Sánchez, J, López, D, Martínez, N, Roselló-Catafau, J, Mitjavila, M T, Puig-Parellada, P
Format: Article
Language:English
Subjects:
Adaptation, Physiological - physiology
Aging - physiology
Animals
Aortic Diseases - etiology
Aortitis - etiology
Aortitis - physiopathology
Dinoprostone - metabolism
Male
Oxidative Stress - physiology
Rats
Rats, Wistar
Superoxide Dismutase - metabolism
Superoxides - metabolism
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Summary:Cells are armed with a vast repertoire of antioxidant defence mechanisms to prevent the accumulation of oxidative damage. The cellular adaptive response is an important antioxidant mechanism against physiological and pathophysiological oxidative alterations in a cell's microenvironment. The aim of this paper was to study, in the rat aorta, whether this adaptive response and the inflammation associated with oxidative stress were expressed throughout the aging process. We examined the rat aorta, as it is a very sensitive tissue to oxidative stress. Male Wistar rats of 1.5, 3, 12, 18 and 24 months of age were used. Superoxide anion (O2(-)) generation; levels of two antioxidant enzymes, superoxide dismutase (SOD) and catalase; and the levels of prostaglandin E2 (PGE2), an inflammatory marker, were measured. The results for rats at different ages were compared with those for 3 months of age. A balance between production of O2(-) and SOD activity was found in the aorta of rats from 1.5 to 12 months old. Oxidative stress was present in the aorta of old animals (18-24 months), due to a failure in the mechanisms of adaptation to oxidative stress. The observed increase in PGE2 levels in these rats reflected an inflammatory response. All together suggest that vascular oxidative stress and the inflammatory process observed in the old groups of rats could be closely related to vascular aging. Our results also remark the importance of the adaptative response to oxidative stress.
ISSN:1138-7548
1877-8755
DOI:10.1007/bf03165787