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Metabotropic glutamate receptor agonists stimulate polyphosphoinositide hydrolysis in primary cultures of rat hepatocytes

  • Francesc Sureda
  • , Agata Copani
  • , Valeria Bruno
  • , Thomas Knöpfel
  • , Gainer Meltzger
  • , Ferdinando Nicoletti*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

23 Citations (Scopus)

Abstract

The metabotropic glutamate (mGlu) receptor agonists, quisqualate and (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid (ACPD), but not (RS)-3,5-dihydroxyphenylglycine or (2S,3S,4S)-α-(carboxycyclopropyl)glycine stimulated [3H]inositolmonophosphate ([3H]InsP) formation in primary cultures of rat hepatocytes. 1S,3R-ACPD-stimulated [3H]InsP formation was inhibited by α-methyl-4-carboxyphenylglycine, indicating that cultured hepatocytes express functional mGlu receptors coupled to polyphosphoinositide hydrolysis. The identity of these receptors is not similar to that of any of the known mGlu receptor subtypes characterized in heterologous expression systems.

Original languageEnglish
Pages (from-to)R1-R2
Number of pages2
JournalEuropean Journal of Pharmacology
Volume338
Issue number2
DOIs
Publication statusPublished - 5 Nov 1997

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 9 - Industry, Innovation, and Infrastructure
    SDG 9 Industry, Innovation, and Infrastructure

User-Defined Keywords

  • Hepatocyte cultured
  • Metabotropic glutamate receptor
  • Polyphosphoinositide hydrolysis

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