Selective activation of phosphoinositide hydrolysis by a rigid analogue of glutamate.

Abstract:

:Ibotenate and trans-D,L-1-amino-1,3-cyclopentanedicarboxylic acid (trans-ACPD) are rigid analogues of glutamate. Ibotenate has been shown to activate phosphoinositide hydrolysis in rat brain slices. We now report that trans-ACPD also stimulates phosphoinositide hydrolysis but with much higher potency and efficacy than ibotenate. The pharmacological profiles, regional distributions, and developmental regulation of the responses to ibotenate and trans-ACPD are similar, suggesting that these agonists act at the same site. However, trans-ACPD is the first agonist described that is selective for this receptor relative to other excitatory amino acid receptor subtypes.

journal_name

Neurosci Lett

journal_title

Neuroscience letters

authors

Desai MA,Conn PJ

doi

10.1016/0304-3940(90)90555-n

subject

Has Abstract

pub_date

1990-02-05 00:00:00

pages

157-62

issue

1-2

eissn

0304-3940

issn

1872-7972

pii

0304-3940(90)90555-N

journal_volume

109

pub_type

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