Simultaneous induction of sod, glutathione reductase, GSH, and ascorbate in liver and kidney correlates with survival during aging

Free Radic Biol Med. 1993 Aug;15(2):133-42. doi: 10.1016/0891-5849(93)90052-v.

Abstract

Catalase was continuously inhibited with aminotriazole in the liver and kidney during 33 months in large populations of old and young frogs in order to study the effects of the modification of the tissue antioxidant/prooxidant balance on the life span of a vertebrate species showing an oxygen consumption rate similar to that of humans. Free-radical-related parameters were measured during three consecutive years at 2.5, 14.5, and 26.5 months of experimentation. Aging per se did not decrease antioxidant enzymes and did not increase peroxidation (thiobarbituric acid positive substances, or high-pressure liquid chromatography [HPLC]-malondialdehyde), either cross sectionally or longitudinally. Long-term catalase inhibition leads to time-dependent increases (100-900%) of endogenous superoxide dismutase, GSH, ascorbate, and especially glutathione reductase at 2.5 and 14.5 months of experimentation. This was positively correlated with a higher survival of treated animals (91% in treated versus 46% in controls at 14.5 months of experimentation). The loss of those inductions after 26.5 months leads to a sharp increase in mortality rate. The results show for the first time that simultaneous induction of various tissue antioxidant enzymes and nonenzymatic antioxidants can increase the mean life span of a vertebrate animal. It is concluded that the tissue antioxidant/prooxidant balance is a strong determinant of mean life span.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / metabolism
  • Animals
  • Ascorbic Acid / biosynthesis*
  • Catalase / antagonists & inhibitors
  • Free Radicals
  • Glutathione / biosynthesis*
  • Glutathione Reductase / biosynthesis*
  • Humans
  • Kidney / growth & development*
  • Kidney / metabolism
  • Liver / growth & development*
  • Liver / metabolism
  • Longevity
  • Oxygen Consumption
  • Ranidae
  • Superoxide Dismutase / biosynthesis*
  • Thiobarbituric Acid Reactive Substances / metabolism

Substances

  • Free Radicals
  • Thiobarbituric Acid Reactive Substances
  • Catalase
  • Superoxide Dismutase
  • Glutathione Reductase
  • Glutathione
  • Ascorbic Acid