Protein metabolism in rats during long-term dietary restriction: influence of aging

JPEN J Parenter Enteral Nutr. 1999 Jan-Feb;23(1):32-7. doi: 10.1177/014860719902300132.

Abstract

Background: Protein depletion is frequent in the elderly, but the underlying mechanisms are not yet fully understood. In particular, it is unknown whether there is a defect of adaptation to a restriction of food intake in the elderly. This study was performed to compare the effects of 6-week dietary restriction (DR) on protein metabolism in both adult and aged rats.

Methods: Adult (3-month-old) and aged (22-month-old) rats were acclimatized for 2 weeks and then fed a standard diet for 6 weeks, either ad libitum (control adult [C(Adult)] and aged [C(Aged)] rats) or with only 50% of the average intake of the second week of acclimatization (restricted adult [R(Adult)] and aged [R(Aged)] rats). Protein metabolism, in terms of tissue protein content, nitrogen balance, and 3-methylhistidine (3-MH) urinary excretion, was evaluated.

Results: C(Adult) rats gained 30.4% of initial weight, whereas the body weight (BW) of C(Aged) rats was maintained. DR induced a rapid decrease in BW during the first 2 weeks in R(Adult) rats, but afterward BW remained stable. In R(Aged) rats, BW loss was linear during the 6 weeks and significantly higher than for R(Adult) rats (p<.01). In both restricted groups, muscle protein content was moderately affected by DR, whereas DR induced a marked decrease in visceral protein content. Nitrogen balance was decreased by DR but stayed positive in R(Adult) rats, whereas it became null in R(Aged) rats.

Conclusions: In terms of protein metabolism, aged rats adapted less efficiently than adult rats to a long-term dietary restriction.

Publication types

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

MeSH terms

  • Aging / metabolism*
  • Analysis of Variance
  • Animals
  • Body Weight
  • Creatinine / urine
  • Dietary Proteins / administration & dosage
  • Dietary Proteins / metabolism*
  • Food Deprivation / physiology*
  • Male
  • Methylhistidines / urine
  • Muscles / metabolism*
  • Organ Size
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Dietary Proteins
  • Methylhistidines
  • Creatinine
  • 3-methylhistidine