beta-N-methylamino-L-alanine is a low-affinity agonist of metabotropic glutamate receptors.

Abstract:

:beta-N-methylamino-L-alanine (L-BMAA) is an excitotoxin whose neurodegenerative effects are associated with its agonist properties at the N-methyl-D-aspartate (NMDA) receptor. We measured the effects of L-BMAA on inositol phosphate (InsP) formation in primary cultured striatal neurons. This culture is almost devoid of glial cells and the pharmacology of glutamate receptors is well-defined. This allowed us to show that L-BMAA induced InsP formation via a direct action at the glutamate metabotropic (Qp) receptors coupled to InsP formation. We demonstrated that L-BMAA is a full-agonist of the Qp receptor, but with a low potency. Therefore, the neurotoxic properties of L-BMAA might implicate the activation of the Qp receptor in association with the NMDA receptor.

journal_name

Neuroreport

journal_title

Neuroreport

authors

Manzoni OJ,Prezeau L,Bockaert J

doi

10.1097/00001756-199110000-00014

subject

Has Abstract

pub_date

1991-10-01 00:00:00

pages

609-11

issue

10

eissn

0959-4965

issn

1473-558X

journal_volume

2

pub_type

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