Comparison of motor reflex and vocalization thresholds following systematically administered morphine, fentanyl, and diazepam in the rat: assessment of sensory and performance variables
Relief of post-herpetic neuralgia with the N-methyl-d-aspartic acid receptor antagonist ketamine: a double-blind, cross-over comparison with morphine and placebo
Baclofen reverses the hypersensitivity of dorsal horn wide dynamic range neurons to mechanical stimulation after transient spinal cord ischaemia — implications for a tonic GABA-ergic control of myelinated fiber input
Kappa-opioid receptor-mediated antinociception in the rat. I. Comparative actions of mu- and kappa-opioids against noxious thermal, pressure and electrical stimuli
Chemically-diverse ligands at the Glycine B site coupled to N-methyl-d-aspartate (NMDA) receptors selectively block the late phase of formalin-induced pain in mice
6-(1H-imidazol-1-yl)-7-nitro-2,3 (1H,4H)-quinoxalinedione hydrochloride (YM 90K) and related compounds: structure-activity relationships for the AMPA-type non-NMDA receptor
2 receptor antagonists: a comparison to other classes of antinociceptive agent, Pain, 65, in press.
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Pre-treatment with MK-801, a non-competitive NMDA antagonist, prevents development of mechanical hyperalgesia in a rat model of chronic neuropathy, but not in a model of chronic inflammation
Systemic excitatory amino acid receptor antagonists of the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor and of the N-methyl-d-aspartate (NMDA) receptor relieve mechanical hypersensitivity after transient spinal cord ischemia in rats
Effects of intrathecal capsaicin and an NK-1 antagonist, CP 96-345, on the thermal hyperalgesia observed following unilateral constriction of the sciatic nerve in the rat