Origin of cocaine- and amphetamine-regulated transcript-containing axons innervating hypophysiotropic corticotropin-releasing hormone-synthesizing neurons in the rat

Endocrinology. 2005 Jul;146(7):2985-91. doi: 10.1210/en.2005-0178. Epub 2005 Apr 14.

Abstract

Cocaine- and amphetamine-regulated transcript (CART) has stimulatory effects on the hypothalamic-pituitary-adrenal axis through direct effects on hypophysiotropic CRH neurons. Recently CART-containing axons have been demonstrated to densely innervate the hypophysiotropic CRH neurons. Based on the sources of the CART-immunoreactive (IR) innervation of the paraventricular nucleus, the putative origins of these CART-containing fibers include neurons of the hypothalamic arcuate nucleus that coexpress alphaMSH and medullary adrenaline-producing neurons. To determine whether these cell groups contribute to the CART innervation of the hypophysiotropic CRH neurons, we performed a quadruple-labeling immunofluorescent study using antisera against CRH, CART, alphaMSH, and phenylethanolamine-N-methyl-transferase (PNMT), the latter as a marker for adrenaline. Consistent with previous observations, PNMT- and CART-IR axons densely innervated all CRH neurons, whereas the alphaMSH-IR innervation was sparse. Although approximately 60% of CART-IR varicosities in juxtaposition to CRH neurons cocontained PNMT, only approximately 18% of them were immunopositive for alphaMSH. All alphaMSH-IR boutons and approximately 90% of PNMT-containing varicosities on the surface of CRH neurons were also labeled for CART. The remaining 22% of CART axon varicosities in contact with CRH neurons contained neither alphaMSH nor PNMT. These results indicate that medullary adrenergic/CART neurons are the major source for the CART innervation of CRH neurons in the paraventricular nucleus; however, to a lesser extent the arcuate nucleus also contributes to the CART-IR innervation of these neurons. The observation that nearly 20% of the CART-IR afferents contain neither alphaMSH nor PNMT, however, suggests that additional sources also contribute to the CART-IR input of hypophysiotropic CRH neurons.

Publication types

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

MeSH terms

  • Animals
  • Arcuate Nucleus of Hypothalamus / cytology
  • Arcuate Nucleus of Hypothalamus / metabolism
  • Axons / metabolism*
  • Cocaine- and Amphetamine-Regulated Transcript Protein
  • Corticotropin-Releasing Hormone / biosynthesis*
  • Corticotropin-Releasing Hormone / physiology
  • Fluorescent Antibody Technique
  • Hypothalamo-Hypophyseal System / physiology*
  • Male
  • Medulla Oblongata / cytology
  • Medulla Oblongata / metabolism
  • Methyltransferases
  • Microscopy, Confocal
  • Nerve Tissue Proteins / metabolism*
  • Neurons / metabolism*
  • Neurotransmitter Agents / metabolism*
  • Phosphatidylethanolamine N-Methyltransferase
  • Pituitary-Adrenal System / physiology*
  • Presynaptic Terminals / metabolism
  • Rats
  • Rats, Wistar
  • Tissue Distribution
  • alpha-MSH / metabolism

Substances

  • Nerve Tissue Proteins
  • Neurotransmitter Agents
  • Cocaine- and Amphetamine-Regulated Transcript Protein
  • alpha-MSH
  • Corticotropin-Releasing Hormone
  • Methyltransferases
  • Phosphatidylethanolamine N-Methyltransferase