Block of P-type Ca2+ channels by the NMDA receptor antagonist eliprodil in acutely dissociated rat Purkinje cells-Reference-Cited by-同舟云学术

Block of P-type Ca2+ channels by the NMDA receptor antagonist eliprodil in acutely dissociated rat Purkinje cells

Published:1995-12 Issue:1 Volume:294 Page:91-100
ISSN:0014-2999
Container-title:European Journal of Pharmacology
language:en
Short-container-title:European Journal of Pharmacology

Author:

Biton Bruno,Granger Patrick,Depoortere Henri,Scatton Bernard,Avenet Patrick

Publisher

Elsevier BV

Subject

Pharmacology

Reference41 articles.

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3. The NMDA receptor antagonist eliprodil (SL 82.0715) blocks Ca2+ channels in acutely dissociated neurons from rat hippocampus and cerebellum;Avenet;Neurosci. Abstr.,1994

4. SB 201823-A, a neuronal Ca2+ antagonist is neuroprotective in two models of cerebral ischaemia;Benham;Neuropharmacology,1993

5. L-type voltage-dependent calcium channels do not modulate aminergic neurotransmitter release induced by transient global cerebral ischaemia: an in vivo microdialysis study in rat;Bentué-Ferrer;Exp. Brain Res.,1993

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1. P/Q-type calcium channel modulators;British Journal of Pharmacology;2012-09-25

2. Ifenprodil reduces excitatory synaptic transmission by blocking presynaptic P/Q type calcium channels;Journal of Neurophysiology;2012-03-15

3. Ifenprodil, a Novel NMDA Receptor Antagonist : Site and Mechanism of Action;Current Drug Targets;2001-09-01

4. The pharmacology of ion channels: with particular reference to voltage-gated Ca2+ channels;European Journal of Pharmacology;1999-06

5. Anticonvulsant effects of eliprodil alone or combined with the glycineB receptor antagonist L-701,324 or the competitive NMDA antagonist CGP 40116 in the amygdala kindling model in rats;Neuropharmacology;1999-02