The formalin test: Scoring properties of the first and second phases of the pain response in rats
Abbott F.V., Franklin K.B.J., Westbrook R.F. The formalin test: scoring properties of the first and second phases of the pain response in rats. Pain. 60:1995;91-102.
Activity of 2,3-benzodiazepines at native rat and recombinant human glutamate receptors in vitro: Stereopsecificity and selectivity profiles
Bleakman D., Ballyk B.A., Schoepp D.D. et al. Activity of 2,3-benzodiazepines at native rat and recombinant human glutamate receptors in vitro: stereopsecificity and selectivity profiles. Neuropharmacology. 35:1996a;1689-1702.
Pharmacological discrimination of GluR5 and GluR6 kainate receptor subtypes by (3S,4aR,6R,8aR)-6-[2-(1(2)H-tetrazole-5-yl)ethyl]decahydroisoquin oline-3 carboxylic-acid
Bleakman D., Schoepp D. D., Ballyk B. et al. Pharmacological discrimination of GluR5 and GluR6 kainate receptor subtypes by (3S,4aR,6R,8aR)-6-[2-(1(2)H-tetrazole-5-yl)ethyl]decahydroisoquin oline-3 carboxylic-acid. Mol. Pharmacol. 49:1996b;581-585.
A comparison of intravenous NBQX and GYKI 53655 as AMPA antagonists in the rat spinal cord
Chizh B.A., Cumberbatch M.J., Headley P.M. A comparison of intravenous NBQX and GYKI 53655 as AMPA antagonists in the rat spinal cord. Br. J. Pharmacol. 112:1994;843-846.
The contribution of excitatory amino acids to central sensitization and persistent nociception after formalin-induced tissue injury
Coderre T.J., Melzack R. The contribution of excitatory amino acids to central sensitization and persistent nociception after formalin-induced tissue injury. J. Neurosci. 12:1992;3665-3670.
Contribution of central plasticity to to pathological pain: Review of clinical and experimental evidence
Coderre T.J., Katz J., Vaccarino A.L., Melzack R. Contribution of central plasticity to to pathological pain: review of clinical and experimental evidence. Pain. 52:1993a;259-285.
The formalin test: A validation of the weighted-scores method of the behavioral pain rating
Coderre T.J., Fundytus M.E., McKenna J.E., Dalal S., Melzack R. The formalin test: a validation of the weighted-scores method of the behavioral pain rating. Pain. 54:1993b;43-50.
Intracelullar messengers contributing to persistent nociception and hyperalgesia induced by L-glutamate and substance P in the rat formalin pain model
Coderre T.J., Yashpal K. Intracelullar messengers contributing to persistent nociception and hyperalgesia induced by L-glutamate and substance P in the rat formalin pain model. Eur. J. Neurosci. 6:1994;1328-1334.
AMPA receptors have an equal role in spinal nociceptive and non-nociceptive transmission
Cumberbatch M.J., Chizh B.A., Headley P.M. AMPA receptors have an equal role in spinal nociceptive and non-nociceptive transmission. Neuroreport. 5:1994;877-880.
Evidence for the involvement of N-methylaspartate receptors in wind-up of class 2 neurons in the dorsal horn of rat
Davies S.N., Lodge D. Evidence for the involvement of N-methylaspartate receptors in wind-up of class 2 neurons in the dorsal horn of rat. Brain Res. 424:1987;402-406.
Evidence for a role of the NMDA receptor in the frequency dependent potentiation of deep rat dorsal horn nociceptive neurons following C fibre stimulation
Dickenson A.H., Sullivan A.F. Evidence for a role of the NMDA receptor in the frequency dependent potentiation of deep rat dorsal horn nociceptive neurons following C fibre stimulation. Neuropharmacology. 26:1987;1235-1238.
GYKI 52466, a 2,3-benzodiazepine, is a highly selective non-competitive antagonist of AMPA/Kainate receptor responses
Donevan S.D., Rogawski M.A. GYKI 52466, a 2,3-benzodiazepine, is a highly selective non-competitive antagonist of AMPA/Kainate receptor responses. Neuron. 10:1993;51-59.
The formalin test: A quantitative study of the analgesic effects of morphine, meperidin and brain stem stimulation in rats and cat
Dubuisson D., Dennis S.G. The formalin test: a quantitative study of the analgesic effects of morphine, meperidin and brain stem stimulation in rats and cat. Pain. 4:1977;161-174.
Primary afferent depolarization in the rat spinal cord is mediated by pathways utilizing NMDA and non-NMDA receptors
Evans R.H., Long S.K. Primary afferent depolarization in the rat spinal cord is mediated by pathways utilizing NMDA and non-NMDA receptors. Neurosci. Lett. 100:1989;231-236.
A comparison of excitatory amino acid antagonists acting at primary afferent C fibers and motoneurons of the isolated spinal cord of the rat
Evans R.H., Evans S.J., Pook P.C., Sunter D.C. A comparison of excitatory amino acid antagonists acting at primary afferent C fibers and motoneurons of the isolated spinal cord of the rat. Br. J. Pharmacol. 91:1987;531-537.
Evidence for spinal N-methyl-D-aspartate receptor involvement in prolonged chemical nociception in the rat
Haley J.E., Sullivan A.F., Dickenson A.H. Evidence for spinal N-methyl-D-aspartate receptor involvement in prolonged chemical nociception in the rat. Brain Res. 518:1990;218-226.
Glutamate receptor channels in DRG neurons: Activation of kainate and quisqualate and blockade of desensitization by concavalin
Huettner J.E. Glutamate receptor channels in DRG neurons: activation of kainate and quisqualate and blockade of desensitization by concavalin. A. Neuron. 5:1990;255-266.
Role of excitatory amino acid receptors in the mediation of the nociceptive response to formalin in the rat
Hunter J.C., Singh L. Role of excitatory amino acid receptors in the mediation of the nociceptive response to formalin in the rat. Neurosci. Lett. 174:1994;217-221.
Structure-activity studies of 6-(tetrazolylalkyl)-substituted decahydroisoquinoline-3-carboxylic acid AMPA receptor antagonists, 1. effects of stereochemistry, chain length and chain substitution
Ornstein P.L., Arnold B.M., Allen N.K. et al. Structure-activity studies of 6-(tetrazolylalkyl)-substituted decahydroisoquinoline-3-carboxylic acid AMPA receptor antagonists, 1. effects of stereochemistry, chain length and chain substitution. J. Med. Chem. 39:1996a;2219-2231.
Structure-activity studies of 6-substituted decahydroisoquinoline-3-carboxylic Acid AMPA receptor antagonists. 2. Effects of distal acid bioisosteric substitution, absolute stereochemical preferences and in vivo activity
Ornstein P.L., Arnold B.M., Allen N.K. et al. Structure-activity studies of 6-substituted decahydroisoquinoline-3-carboxylic Acid AMPA receptor antagonists. 2. Effects of distal acid bioisosteric substitution, absolute stereochemical preferences and in vivo activity. J. Med. Chem. 39:1996b;2232-2244.
Selective modulation of desensitization at AMPA versus kainate receptors by cyclothiazide and concanavalin
Partin K.M., Patneau D.K., Winter C.A., Mayer M.L., Buonanno A. Selective modulation of desensitization at AMPA versus kainate receptors by cyclothiazide and concanavalin. A. Neuron. 11:1993;1069-1082.
Selective antagonism of AMPA receptors unmasks kainate receptor-mediated responses in hippocampal neurons
Paternain A.V., Morales M., Lerma J. Selective antagonism of AMPA receptors unmasks kainate receptor-mediated responses in hippocampal neurons. Neuron. 14:1995;185-189.
Analgesic effects of AMPA/kainate antagonist LY293558 in humans: Reduction of capsaicin-evoked allodynia and hyperalgesia but not pain sensations in normal skin
Sang C.N., Hostetter M., Gracely R. et al. Analgesic effects of AMPA/kainate antagonist LY293558 in humans: reduction of capsaicin-evoked allodynia and hyperalgesia but not pain sensations in normal skin. Soc. Neurosci. Abstr. 23:1997;1015.
In vitro and in vivo antagonism of AMPA receptor activation by (3S,4aR,6R,8aR)-6-[2-(1(2)H-Tetrazyl)-5-yl)ethyl]decahydro-isoqui noline-3-carboxylic acid
Schoepp D.D., Lodge D., Bleakman D. et al. In vitro and in vivo antagonism of AMPA receptor activation by (3S,4aR,6R,8aR)-6-[2-(1(2)H-Tetrazyl)-5-yl)ethyl]decahydro-isoqui noline-3-carboxylic acid. Neuropharmacology. 34:1995;1159-1168.
Structure-activity relationships of 2,3, benzodiazepine compounds with glutamate antagonistic action
Tarnawa I., Berzsenyi P., Andrási F., Botka P., Hámori T., Ling I., Körösi J. Structure-activity relationships of 2,3, benzodiazepine compounds with glutamate antagonistic action. Biorganic Med. Chem. Lett. 3:1993;99-104.
Modulation of spinal excitability; Co-operation between neurokinin and excitatory amino-acid neurotransmitters
Urban L., Thompson S.W.N., Dray A. Modulation of spinal excitability; co-operation between neurokinin and excitatory amino-acid neurotransmitters. Trends Neurosci. 17:1994;432-438.
The induction and maintenance of central sensitization is dependent on N-methyl-D-aspartic acid receptor activation: Implications for post-injury pain hypersensitivity states
Woolf C.J., Thompson S.W.N. The induction and maintenance of central sensitization is dependent on N-methyl-D-aspartic acid receptor activation: implications for post-injury pain hypersensitivity states. Pain. 44:1991;293-299.
A benzodiazepine recognition site associated with the non-NMDA glutamate receptor
Zorumski C.F., Yamada K.A., Price M.T., Olney J.W. A benzodiazepine recognition site associated with the non-NMDA glutamate receptor. Neuron. 10:1993;61-67.