The trophic effect of beta-amyloid 25-35 peptide is not mediated by NK1 or bombesin receptors

Neuroreport. 1992 Dec;3(12):1131-4. doi: 10.1097/00001756-199212000-00025.

Abstract

beta-Amyloid peptide and spantide have previously been described to have trophic effects on hippocampal neurones in vitro. We report here that bombesin and [Pro9]-substance P also show a neurotrophic effect on cultured hippocampal neurones. The neurotrophic effect of spantide or a beta-amyloid fragment containing amino acids 25 to 35 was not blocked by addition of the NK1 receptor agonist, substance P or the nonpeptide NK1 antagonist, RP 67580. For the bombesin-related peptides, the antagonist [Tyr4-DPhe12]-bombesin also provokes a trophic response, but the agonist alytesin and the antagonist [Leu13-psi-(CH2NH) Leu14]-bombesin have no effect on neurite growth. These results suggest that the observed trophic responses are unlikely to be mediated by a classical NK1 or bombesin receptor.

MeSH terms

  • Amino Acid Sequence
  • Amyloid beta-Peptides / pharmacology*
  • Animals
  • Bombesin / analogs & derivatives
  • Bombesin / pharmacology
  • Cells, Cultured
  • Chromatography, High Pressure Liquid
  • Female
  • Hippocampus / cytology
  • Hippocampus / drug effects
  • Molecular Sequence Data
  • Neurons / drug effects
  • Peptide Fragments / pharmacology*
  • Pregnancy
  • Rats
  • Receptors, Bombesin
  • Receptors, Neurokinin-2
  • Receptors, Neurotransmitter / drug effects*
  • Substance P / pharmacology

Substances

  • Amyloid beta-Peptides
  • Peptide Fragments
  • Receptors, Bombesin
  • Receptors, Neurokinin-2
  • Receptors, Neurotransmitter
  • amyloid beta-protein (25-35)
  • Substance P
  • Bombesin