Age-related alterations in tanycytes of the mediobasal hypothalamus of the male rat

Neurobiol Aging. 1995 Jan-Feb;16(1):77-83. doi: 10.1016/0197-4580(95)80010-o.

Abstract

By means of semiquantitative immunocytochemistry, possible age-related changes in dopamine and cyclic AMP-regulated phosphoprotein mr 32 (DARPP-32) and glial fibrillary acidic protein (GFAP) immunoreactivities (IR) were investigated in tanycytes of the arcuate nucleus. These two markers showed opposite changes during aging. DARPP-32 IR decreased by around 70%, whereas GFAP IR increased by around 300% in 24-month-old vs. 3-month-old rats. These changes were accompanied by a progressive loss in the number of tanycytes, measured by counting of their long processes in the arcuate nucleus. No significant age-related change was observed either in GFAP IR in astrocytic populations of the mediobasal hypothalamus or in tyrosine hydroxylase IR in dopaminergic neurons of the dorsal arcuate nucleus. These observations indicate that the tanycytic population of the arcuate nucleus undergoes important modifications during aging, which include cell loss, impairment in the intracellular signalling cascade linked to DARPP-32, and hypertrophy. These changes may be related to the alterations in the neuroendocrine systems known to occur during aging.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / metabolism
  • Aging / pathology*
  • Animals
  • Arcuate Nucleus of Hypothalamus / metabolism
  • Arcuate Nucleus of Hypothalamus / pathology
  • Astrocytes / metabolism
  • Dopamine and cAMP-Regulated Phosphoprotein 32
  • Glial Fibrillary Acidic Protein / metabolism
  • Hypothalamus, Middle / cytology
  • Hypothalamus, Middle / metabolism
  • Hypothalamus, Middle / pathology*
  • Image Processing, Computer-Assisted
  • Immunohistochemistry
  • Male
  • Nerve Tissue Proteins / metabolism
  • Paraventricular Hypothalamic Nucleus / pathology
  • Phosphoproteins / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Dopamine and cAMP-Regulated Phosphoprotein 32
  • Glial Fibrillary Acidic Protein
  • Nerve Tissue Proteins
  • Phosphoproteins
  • Tyrosine 3-Monooxygenase