Search Results - "Woodruff, G. N."
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1
The antiepileptic agent gabapentin (Neurontin) possesses anxiolytic-like and antinociceptive actions that are reversed by D-serine
Published in Psychopharmacologia (01-09-1996)“…This report describes the activity of the antiepileptic agent gabapentin (Neurontin) in animal models predictive of anxiolysis and analgesia. Gabapentin…”
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2
Systemic administration of MK-801 protects against ischemia-induced hippocampal neurodegeneration in the gerbil
Published in The Journal of neuroscience (01-10-1987)“…The neuroprotective effects of MK-801, a noncompetitive antagonist of N-methyl-D-aspartate (NMDA) receptors, were evaluated in models of cerebral ischemia…”
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3
Development of a Class of Selective Cholecystokinin Type B Receptor Antagonists Having Potent Anxiolytic Activity
Published in Proceedings of the National Academy of Sciences - PNAS (01-09-1990)“…PD134308 and PD135158 are potent and selective antagonists at the cholecystokinin type B (CCK-B) receptors with IC50values of 1.6 nM and 3.5 nM, respectively,…”
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4
The Anticonvulsant MK-801 is a Potent N-methyl-D-aspartate Antagonist
Published in Proceedings of the National Academy of Sciences - PNAS (01-09-1986)“…The compound MK-801 {(+)-5-methyl-10,11- dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine maleate)} is a potent anticonvulsant that is active after oral…”
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5
7-Chlorokynurenic Acid is a Selective Antagonist at the Glycine Modulatory Site of the N-methyl-D-aspartate Receptor Complex
Published in Proceedings of the National Academy of Sciences - PNAS (01-09-1988)“…Glycine markedly potentiates N-methyl-D-aspartate (N-Me-D-Asp) responses in mammalian neurons by an action at a modulatory site on the N-Me-D-Asp…”
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6
Evidence for an Involvement of the Brain Cholecystokinin B Receptor in Anxiety
Published in Proceedings of the National Academy of Sciences - PNAS (15-02-1991)“…The effect of neuropeptide cholecystokinin (CCK) receptor agonists and antagonists was examined in the rat elevated X-maze model of anxiety. The selective…”
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7
Cholecystokinin antagonists
Published in Annual review of pharmacology and toxicology (01-01-1991)Get full text
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8
Autoradiographic localization and biochemical characterization of peripheral type CCK receptors in rat CNS using highly selective nonpeptide CCK antagonists
Published in The Journal of neuroscience (01-09-1987)“…Two potent and highly selective nonpeptide antagonists, L-365,031 [1-methyl-3-(4-bromobenzoyl)amino-5-phenyl-3H-1,4 benzodiazepin-2-one] and 3H-L-364,718…”
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9
Protective effect of the glutamate antagonist, MK-801 in focal cerebral ischemia in the cat
Published in Journal of cerebral blood flow and metabolism (01-02-1988)“…The effects of the glutamate N-methyl-D aspartate (NMDA) receptor antagonist, MK-801, upon ischemic brain damage has been examined in anesthetized cats. Focal…”
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10
MK-801 is neuroprotective in gerbils when administered during the post-ischaemic period
Published in Neuroscience (01-06-1988)“…The neuroprotective effects of the non-competitive N-methyl-D-aspartate receptor antagonist (+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine…”
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11
Characterisation of [3H]gabapentin binding to a novel site in rat brain: homogenate binding studies
Published in European journal of pharmacology (15-02-1993)“…The binding characteristics of [3H]gabapentin, the radiolabelled analogue of the novel anticonvulsant gabapentin (1-(aminomethyl)cyclohexaneacetic acid) were…”
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12
Cholecystokinin modulates the release of dopamine from the anterior and posterior nucleus accumbens by two different mechanisms
Published in Journal of neurochemistry (01-03-1991)“…The effects of various cholecystokinin (CCK)-related peptides were investigated on 35 mM K(+)-stimulated endogenous dopamine release from slices of either…”
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13
The neuroprotective action of dizocilpine (MK‐801) in the rat middle cerebral artery occlusion model of focal ischaemia
Published in British journal of pharmacology (01-08-1991)“…1 An acute model of focal ischaemia, which involves permanent occlusion of the middle cerebral artery of the rat with 4 h survival, was used to find the…”
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14
The neuroprotective actions of kynurenic acid and MK-801 in gerbils are synergistic and not related to hypothermia
Published in European journal of pharmacology (06-02-1990)“…The broad spectrum excitatory amino acid antagonist, kynurenic acid was evaluated in a transient forebrain ischaemia model in gerbils. When administered i.p.,…”
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15
Localization of [3H]gabapentin to a novel site in rat brain: autoradiographic studies
Published in European journal of pharmacology (15-02-1993)“…The autoradiographical distribution of [3H]gabapentin, the tritiated analogue of the novel anticonvulsant gabapentin (1-(aminomethyl)cyclohexaneacetic acid)…”
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16
[3H]MK-801 labels a site on the N-methyl-D-aspartate receptor channel complex in rat brain membranes
Published in Journal of neurochemistry (01-01-1988)“…The potent noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist [3H]MK-801 bound with nanomolar affinity to rat brain membranes in a reversible,…”
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17
The behavioural properties of CI‐988, a selective cholecystokininB receptor antagonist
Published in British journal of pharmacology (01-09-1991)“…1 The behavioural effects of a selective cholecystokininB (CCKB) receptor antagonist CI‐988 were investigated in rodents. 2 In three rodent tests of anxiety…”
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Spermine modulation of specific [3H]‐gabapentin binding to the detergent‐solubilized porcine cerebral cortex α2δ calcium channel subunit
Published in British journal of pharmacology (01-02-1997)“…Recent studies have identified the [3H]‐gabapentin‐binding protein, purified from porcine cerebral cortical membranes, as the α2δ subunit of voltage‐sensitive…”
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Comparison of the autoradiographic binding distribution of [3H]‐gabapentin with excitatory amino acid receptor and amino acid uptake site distributions in rat brain
Published in British journal of pharmacology (01-06-1996)“…1 Gabapentin is a novel anticonvulsant with an unknown mechanism of action. Recent homogenate binding studies with [3H]‐gabapentin have suggested a…”
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The interaction of the NK1 receptor antagonist CP‐96,345 with L‐type calcium channels and its functional consequences
Published in British journal of pharmacology (01-09-1993)“…1 We investigated the effects of the non‐peptide NK1 receptor antagonist, CP‐96,345, its inactive enantiomer CP‐96,344, and the racemic mixture (±)‐CP‐96,345,…”
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