An NPY-like peptide may function as MSH-release inhibiting factor in Xenopus laevis

Peptides. 1987 Jan-Feb;8(1):61-7. doi: 10.1016/0196-9781(87)90166-5.

Abstract

This study demonstrates the presence of a rich plexus of neuropeptide Y (NPY) immunoreactive fibers in the hypothalamus and in the intermediate lobe of the pituitary of Xenopus laevis. During superfusion of neurointermediate lobe tissue, synthetic NPY induces a rapid, powerful and dose-dependent inhibition of in vitro release of MSH, endorphin and other proopiomelanocortin (POMC) derived peptides. Therefore, NPY undoubtedly is one of the growing number of neuropeptides that are likely involved in control of the amphibian MSH cells. Although a number of stimulatory neuropeptides have been found, this is the first neuropeptide to apparently function through an inhibitory mechanism. In that a 2-hr treatment with NPY did not influence POMC biosynthesis, nor processing of this prohormone to smaller peptides, we conclude that the primary action of NPY is a direct effect on the secretory process of the MSH cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Endorphins / metabolism*
  • Histocytochemistry
  • Immunoenzyme Techniques
  • In Vitro Techniques
  • MSH Release-Inhibiting Hormone*
  • Melanocyte-Stimulating Hormones / metabolism*
  • Neuropeptide Y / analysis
  • Neuropeptide Y / physiology*
  • Pituitary Gland / metabolism*
  • Pro-Opiomelanocortin / metabolism
  • Radioimmunoassay
  • Xenopus laevis

Substances

  • Endorphins
  • Neuropeptide Y
  • Pro-Opiomelanocortin
  • Melanocyte-Stimulating Hormones
  • MSH Release-Inhibiting Hormone