Structural requirements for neuropeptide Y in mast cell and G protein activation

Eur J Pharmacol. 1995 Mar 15;289(1):125-33. doi: 10.1016/0922-4106(95)90177-9.

Abstract

Incubation of neuropeptide Y or its C-terminal fragments with rat peritoneal mast cells resulted in a dose-dependent histamine release. Fragment 18-36 of neuropeptide Y was the most biologically active peptide. EC25 value on rat mast cells was 7.2 +/- 2.2 nM. Neuropeptide Y was also able to induce a flare response after intradermal injection in humans. The histamine releasing effects of neuropeptide Y related peptides were greatly inhibited by pretreatment of rat mast cells with pertussis toxin or benzalkonium chloride. Neuropeptide Y and C-terminal related peptides also stimulated the GTPase activity of purified heterotrimeric G proteins in a dose-dependent manner from 1 to 50 microM. Binding studies with [125I]neuropeptide Y were unable to provide evidence for the presence of specific binding sites on the surface of mast cells. The alpha helical conformation of neuropeptide Y fragments was studied by measuring the circular dichroism spectra. Neuropeptide Y-(18-36) was the smallest fragment having a strong helical conformation. Our results demonstrate that neuropeptide Y activates mast cells through a non-specific process leading to G protein activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Circular Dichroism
  • GTP-Binding Proteins / drug effects*
  • GTP-Binding Proteins / physiology
  • Histamine Release / drug effects
  • Humans
  • In Vitro Techniques
  • Male
  • Mast Cells / drug effects*
  • Mast Cells / physiology
  • Molecular Sequence Data
  • Neuropeptide Y / analogs & derivatives*
  • Neuropeptide Y / chemistry
  • Neuropeptide Y / pharmacology
  • Neuropeptide Y / physiology
  • Peptide Fragments / pharmacology
  • Protein Structure, Secondary
  • Rats
  • Rats, Wistar
  • Skin / drug effects
  • Skin / immunology
  • Structure-Activity Relationship

Substances

  • Neuropeptide Y
  • Peptide Fragments
  • GTP-Binding Proteins