The NMDA-receptor antagonist CPP abolishes neurogenic 'wind-up pain' after intrathecal administration in humans
about
The importance of stimulus configuration for temporal summation of first and second pain to repeated heat stimuli.The spinal biology in humans and animals of pain states generated by persistent small afferent inputWind-up and the NMDA receptor complex from a clinical perspective.Indirect modulation of dopamine D2 receptors as potential pharmacotherapy for schizophrenia: II. Glutamate (Ant)agonists.N-methyl-D-aspartate receptors and large conductance calcium-sensitive potassium channels inhibit the release of opioid peptides that induce mu-opioid receptor internalization in the rat spinal cord.Targeting the NMDA receptor subunit NR2B for the treatment of neuropathic painThe biochemical womb of schizophrenia: A review.NMDA receptor function, memory, and brain aging.The NMDA (N-methyl-D-aspartate) receptor antagonist memantine in the treatment of postherpetic neuralgia: a double-blind, placebo-controlled study.Intervention with spinal NMDA, adenosine, and NO systems for pain modulation.Future trends in the development of local drug delivery systems: intraspinal, intracerebral, and intraparenchymal therapies.Novel pharmacological strategies for analgesia.Antinociceptive effects of the marine snail peptides conantokin-G and conotoxin MVIIA alone and in combination in rat models of pain.Temporal regularity determines the impact of electrical stimulation on tactile reactivity and response to capsaicin in spinally transected rats.Effects of a partial agonist and a full antagonist acting at the glycine site of the NMDA receptor on inflammation-induced mechanical hyperalgesia in rats.Brain but not spinal NR2B receptor is responsible for the anti-allodynic effect of an NR2B subunit-selective antagonist CP-101,606 in a rat chronic constriction injury model.Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR.Chronic pain and impaired glial glutamate transporter function in lupus-prone mice are ameliorated by blocking macrophage colony-stimulating factor-1 receptors.Involvement of spinal calcitonin gene-related peptide in the development of acute visceral hyperalgesia in the rat.Isoflurane and propofol block neurotoxicity caused by MK-801 in the rat posterior cingulate/retrosplenial cortex.Neurotransmitter alterations in the anterior cingulate cortex in Crohn's disease patients with abdominal pain: A preliminary MR spectroscopy study
P2860
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P2860
The NMDA-receptor antagonist CPP abolishes neurogenic 'wind-up pain' after intrathecal administration in humans
description
1992 nî lūn-bûn
@nan
1992 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
The NMDA-receptor antagonist C ...... hecal administration in humans
@ast
The NMDA-receptor antagonist C ...... hecal administration in humans
@en
The NMDA-receptor antagonist C ...... hecal administration in humans
@nl
type
label
The NMDA-receptor antagonist C ...... hecal administration in humans
@ast
The NMDA-receptor antagonist C ...... hecal administration in humans
@en
The NMDA-receptor antagonist C ...... hecal administration in humans
@nl
prefLabel
The NMDA-receptor antagonist C ...... hecal administration in humans
@ast
The NMDA-receptor antagonist C ...... hecal administration in humans
@en
The NMDA-receptor antagonist C ...... hecal administration in humans
@nl
P1433
P1476
The NMDA-receptor antagonist C ...... hecal administration in humans
@en
P2093
B Svensson
J D Kristensen
P304
P356
10.1016/0304-3959(92)90266-E
P407
P577
1992-11-01T00:00:00Z