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

J Physiol Biochem. 2007 Sep;63(3):239-47. doi: 10.1007/BF03165787.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 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

Substances

  • Superoxides
  • Superoxide Dismutase
  • Dinoprostone