Young little mice express a premature cardiovascular aging phenotype

J Gerontol A Biol Sci Med Sci. 2014 Feb;69(2):152-9. doi: 10.1093/gerona/glt055. Epub 2013 May 16.

Abstract

To investigate the effect of growth hormone and insulin-like growth factor 1 deficiency on the aging mouse arterial system, we compared the hemodynamics in young (4 months) and old (30 months) growth hormone-releasing hormone receptor null dwarf (Little) mice and their wild-type littermates. Young Little mice had significantly lower peak and mean aortic velocity and significantly higher aortic impedance than young wild-type mice. However, unlike the wild-type mice, there were no significant changes in arterial function with age in the Little mice. Aortic pulse wave velocity estimated using characteristic impedance increased with age in the wild-type mice, but it changed minimally in the Little mouse. We therefore conclude that arterial function in Little mice expresses a premature aging phenotype at young age and may neither enhance nor reduce their longevity.

Keywords: Aortic impedance; Cardiovascular function; GH/IGF-1 deficiency; Longevity.; Pulse wave velocity.

Publication types

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

MeSH terms

  • Aging / physiology*
  • Aging, Premature / etiology*
  • Animals
  • Aorta / growth & development*
  • Aorta / physiopathology*
  • Arterial Pressure / physiology
  • Blood Flow Velocity / physiology
  • Growth Hormone / physiology*
  • Insulin-Like Growth Factor I / physiology*
  • Mice
  • Mice, Mutant Strains
  • Phenotype

Substances

  • Insulin-Like Growth Factor I
  • Growth Hormone