Abstract
The (+) isomer of ketamine was approximately 3 and 1.5 times as potent as the (-) isomer in reducing excitation of rat and cat Renshaw cells by N-methylaspartate (NMA) and acetylcholine (ACh) respectively. The potency ratio of the two isomers of ketamine as NMA antagonists was similar to that obtained in anaesthetic and analgesic tests [16, 19, 25].
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetylcholine / pharmacology*
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Action Potentials / drug effects
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Animals
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Aspartic Acid / analogs & derivatives*
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Aspartic Acid / pharmacology
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Cats
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Ketamine / pharmacology*
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N-Methylaspartate
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Neurons / drug effects
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Neurons / physiology*
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Rats
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Spinal Cord / physiology*
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Stereoisomerism
Substances
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Aspartic Acid
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N-Methylaspartate
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Ketamine
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Acetylcholine