d-Morphine, but not l-morphine, has low micromolar affinity for the non-competitive N-methyl-d-aspartate site in rat forebrain. Possible clinical implications for the management of neuropathic pain

Author:

Stringer Mark,Makin Matthew K,Miles John,Morley John S

Publisher

Elsevier BV

Subject

General Neuroscience

Reference19 articles.

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2. Open-channel block of NMDA responses by memantine: therapeutic advantage against NMDA receptor-mediated neurotoxicity;Chen;J. Neurosci.,1992

3. Morphine with dextromethorphan: conversion from other opioid analgesics;Chevlen;J. Pain Sympt. Manage.,2000

4. Differential effects of dextrorphan and levorphanol on the excitation of rat spinal neurons by amino acids;Church;Eur. J. Pharmacol.,1985

5. Serotonin and norepinephrine uptake inhibiting activity of centrally acting analgesics: structural determinants and role in antinociception;Codd;J. Pharmacol. Exp. Ther.,1995

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