Effect of housing rats within a pyramid on stress parameters

Indian J Exp Biol. 2003 Nov;41(11):1289-93.

Abstract

The Giza pyramids of Egypt have been the subject of much research. Pyramid models with the same base to height ratio as of the Great Pyramid of Giza, when aligned on a true north-south axis, are believed to generate, transform and transmit energy. Research done with such pyramid models has shown that they induced greater relaxation in human subjects, promoted better wound healing in rats and afforded protection against stress-induced neurodegnerative changes in mice. The present study was done to assess the effects of housing Wistar rats within the pyramid on the status of oxidative damage and antioxidant defense in their erythrocytes and cortisol levels in their plasma. Rats were housed in cages under standard laboratory conditions. Cages were left in the open (normal control), under a wooden pyramid model (experimental rats) or in a cubical box of comparable dimensions (6 hr/day for 14 days). Erythrocyte malondialdehyde and plasma cortisol levels were significantly decreased in rats kept within the pyramid as compared to the normal control and those within the square box. Erythrocyte reduced glutathione levels, erythrocyte glutathione peroxidase and superoxide dismutase activities were significantly increased in the rats kept in the pyramid as compared to the other two groups. There was no significant difference in any of the parameters between the normal control and rats kept in the square box. The results showed that exposure of adult female Wistar rats to pyramid environment reduces stress oxidative stress and increases antioxidant defense in them.

Publication types

  • Comparative Study

MeSH terms

  • Animal Husbandry
  • Animals
  • Antioxidants / metabolism*
  • Egypt
  • Erythrocytes / metabolism*
  • Female
  • Glutathione Peroxidase / metabolism
  • Housing, Animal*
  • Hydrocortisone / blood*
  • Malondialdehyde / metabolism
  • Mysticism
  • Oxidative Stress*
  • Rats
  • Rats, Wistar / physiology*
  • Superoxide Dismutase / metabolism

Substances

  • Antioxidants
  • Malondialdehyde
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Hydrocortisone