Noncompetitive Metabotropic Glutamate5Receptor Antagonist (E)-2-Methyl-6-styryl-pyridine (SIB1893) Depresses Glutamate Release through Inhibition of Voltage-Dependent Ca2+Entry in Rat Cerebrocortical Nerve Terminals (Synaptosomes)-Reference-Cited by-同舟云学术

Noncompetitive Metabotropic Glutamate5Receptor Antagonist (E)-2-Methyl-6-styryl-pyridine (SIB1893) Depresses Glutamate Release through Inhibition of Voltage-Dependent Ca2+Entry in Rat Cerebrocortical Nerve Terminals (Synaptosomes)

Published:2004-02-24 Issue:3 Volume:309 Page:951-958
ISSN:0022-3565
Container-title:Journal of Pharmacology and Experimental Therapeutics
language:en
Short-container-title:J Pharmacol Exp Ther

Author:

Wang Su-Jane,Sihra Talvinder S.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference40 articles.

1. Role of Group I Metabotropic Glutamate Receptors in Traumatic Spinal Cord White Matter Injury

2. Neuroprotective activity of the potent and selective mGlu1a metabotropic glutamate receptor antagonist, (+)-2-methyl-4 carboxyphenylglycine (LY367385): comparison with LY357366, a broader spectrum antagonist with equal affinity for mGlu1a and mGlu5 receptors

3. Activation of metabotropic glutamate receptors coupled to inositol phospholipid hydrolysis amplifies NMDA-induced neuronal degeneration in cultured cortical cells

4. Selective blockade of metabotropic glutamate receptor subtype 5 is neuroprotective

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