The growth hormone receptor gene-disrupted mouse fails to respond to an intermittent fasting diet

Aging Cell. 2009 Dec;8(6):756-60. doi: 10.1111/j.1474-9726.2009.00520.x. Epub 2009 Sep 11.

Abstract

The interaction of longevity-conferring genes with longevity-conferring diets is poorly understood. The growth hormone receptor gene-disrupted (GHR-KO) mouse is long lived; and this longevity is not responsive to 30% caloric restriction, in contrast to wild-type animals from the same strain. To determine whether this may have been limited to a particular level of dietary restriction, we subjected GHR-KO mice to a different dietary restriction regimen, an intermittent fasting diet. The intermittent fasting diet increased the survivorship and improved insulin sensitivity of normal males, but failed to affect either parameter in GHR-KO mice. From the results of two paradigms of dietary restriction, we postulate that GHR-KO mice would be resistant to any manner of dietary restriction; potentially due to their inability to further enhance insulin sensitivity. Insulin sensitivity may be a mechanism and/or a marker of the lifespan extending potential of an intervention.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Body Weight
  • Fasting*
  • Female
  • Gene Expression Regulation*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Somatotropin / deficiency
  • Receptors, Somatotropin / genetics
  • Receptors, Somatotropin / metabolism*
  • Sex Characteristics

Substances

  • Blood Glucose
  • Receptors, Somatotropin