Functional receptors for vasoactive intestinal polypeptide in cultured astroglia from neonatal rat brain

Pierre J. Magistretti*, Marston Manthorpe, Floyd E. Bloom, Silvio Varon

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

119 Scopus citations

Abstract

The effects of vasoactive intestinal polypeptide (VIP) were assessed on astroglia cultured from rat CNS. In these cultures VIP (500 nM) promoted the hydrolysis of [3H]glycogen newly synthesized from [3H]glucose. This effect on [3H]glycogen levels was also observed with the structurally related peptide PHI-27 and with other substances which had been demonstrated to promote glycogenolysis in rodent CNS in vitro such as: norepinephrine (NE), serotonin, histamine, adenosine, K+ and dibutyryl cyclic-AMP (dbcAMP). Furthermore, VIP (500 nM) and PHI 27 (500 nM), when applied to astroglial cultures in serum-free medium, displayed marked effects on the morphological appearance of the cell population: they converted the flat cells present in the cultures into cells with typical astrocytic morphology. As previously reported, this effect on the cellular morphology of the cultures was also observed, under identical experimental conditions, after NE and dbcAMP application. These studies demonstrate that cultured rat neonatal astroglia possess receptors for VIP, and suggest that a cyclic AMP accumulation may mediate both the metabolic and morphologic components of this response.

Original languageEnglish (US)
Pages (from-to)71-80
Number of pages10
JournalRegulatory Peptides
Volume6
Issue number1
DOIs
StatePublished - Apr 1983
Externally publishedYes

Keywords

  • adenosine
  • astroglia cultures
  • glycogenolysis
  • histamine
  • norepinephrine
  • serotonin

ASJC Scopus subject areas

  • Endocrinology
  • Cellular and Molecular Neuroscience
  • Biochemistry
  • Physiology
  • Clinical Biochemistry

Fingerprint

Dive into the research topics of 'Functional receptors for vasoactive intestinal polypeptide in cultured astroglia from neonatal rat brain'. Together they form a unique fingerprint.

Cite this