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1 5)H(7)N(3)O(5)), a known but rare agonist of excitatory amino acid receptors.
2 mate receptors (mGluRs) are a major class of excitatory amino acid receptors.
3 of non-N-methyl-D-aspartate (NMDA) and NMDA excitatory amino acid receptors.
4 ral substrates that interact at the level of excitatory amino acid receptor activation and subsequent
5 ections (50 nl) of smaller concentrations of excitatory amino acid receptor agonists (e.g., NMDA, KA
6 e presence of important interactions between excitatory amino acid receptors and mu-opioid receptors
7 sult in activation of central nervous system excitatory amino acid receptors and subsequent intracell
8 was characterized in vitro for antagonism of excitatory amino acid receptors, and subsequently tested
9 Bilateral injections of the broad-spectrum excitatory amino acid receptor antagonist kynurenate (Ky
13 upport the potential efficacy of competitive excitatory amino acid receptor antagonists in the treatm
14 5HT1F and 5HT1D receptor agonists, glutamate excitatory amino acid receptor antagonists, nitric oxide
15 was to determine if a change in brain tissue excitatory amino acid receptor binding occurs during pre
17 results suggest that d-amphetamine increases excitatory amino acid receptor function temporarily by r
18 ccinate (ABHS), a neurosteroid that inhibits excitatory amino acid receptor function, in a rabbit rev
19 e N-methyl-D-aspartate (NMDA) subtype of the excitatory amino acid receptor has been implicated in se
20 developmental changes in the distribution of excitatory amino acid receptors in the chicken's auditor
21 nuation), or by prior blockade of ionotropic excitatory amino acid receptors in the commNTS with kynu
22 ere used to determine if the distribution of excitatory amino acid receptors in the owl's auditory br
23 fects of glutamate by inhibition of neuronal excitatory amino acid receptors, including the N-methyl-
25 teroids, which act as negative modulators of excitatory amino acid receptors, may improve behavioral
27 The effects of prolonged ethanol exposure on excitatory amino acid receptor stimulated nitric oxide (
28 onal interactions between opiate ligands and excitatory amino acid receptors, the ultrastructural loc
31 of kynurenate, a wide-spectrum antagonist of excitatory amino acid receptors, while xanthurenate, an
32 targeted the N-methyl-D-aspartic acid (NMDA) excitatory amino acid receptor with an AAV-delivered ant
33 njection of L-S-nitrosocysteine, blockade of excitatory amino acid receptors with kynurenic acid inhi
34 lar distribution of the different classes of excitatory amino acid receptors with respect to the nora
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