Ifenprodil reduces excitatory synaptic transmission by blocking presynaptic P/Q type calcium channels.

Abstract:

:Ifenprodil is a selective blocker of NMDA receptors that are heterodimers composed of GluN1/GluN2B subunits. This pharmacological profile has been extensively used to test the role of GluN2B-containing NMDA receptors in learning and memory formation. However, ifenprodil has also been reported to have actions at a number of other receptors, including high voltage-activated calcium channels. Here we show that, in the basolateral amygdala, ifenprodil dose dependently blocks excitatory transmission to principal neurons by a presynaptic mechanism. This action of ifenprodil has an IC(50) of ~10 μM and is fully occluded by the P/Q type calcium channel blocker ω-agatoxin. We conclude that ifenprodil reduces synaptic transmission in the basolateral amygdala by partially blocking P-type voltage-dependent calcium channels.

journal_name

J Neurophysiol

authors

Delaney AJ,Power JM,Sah P

doi

10.1152/jn.01066.2011

subject

Has Abstract

pub_date

2012-03-01 00:00:00

pages

1571-5

issue

6

eissn

0022-3077

issn

1522-1598

pii

jn.01066.2011

journal_volume

107

pub_type

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