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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1988-7-29
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pubmed:abstractText |
The behavioral effects of MK-801 [(+)-5-methyl-10,11-dihydroxy-5H-dibenzo(a,d)cyclohepten-5,10-imin e], a proposed noncompetitive N-methyl-D-aspartate (NMDA) antagonist, were compared to those of phencyclidine (PCP). In pigeons, MK-801 produced PCP-like catalepsy (i.e., loss of righting without eye closure and without muscle relaxation) and PCP-like discriminative stimulus effects. In rats, MK-801 produced PCP-like behavior (i.e., locomotion, sniffing, swaying and falling). In rhesus monkeys, like PCP, MK-801 produced 1) ketamine-like discriminative stimulus effects, 2) positive reinforcing effects and 3) ketamine-like anesthetic effects (i.e., anesthesia without eye closure and without respiratory depression, but with profuse salivation and with some muscle relaxation). Thus, MK-801 produced PCP-like behavioral effects in each species and with each procedure. MK-801 was 2 to 10 times more potent than PCP, depending on the effect measured and the species tested. Because MK-801 has been shown to have NMDA-antagonist properties, the findings of this study offer further support for the hypothesis that certain behavioral effects of PCP-like drugs may result from a reduction of neurotransmission at excitatory synapses utilizing NMDA-preferring receptors. The behavioral similarities between MK-801 and PCP make it relevant to evaluate PCP-like activity in clinical trials of MK-801.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anticonvulsants,
http://linkedlifedata.com/resource/pubmed/chemical/Aspartic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Dibenzocycloheptenes,
http://linkedlifedata.com/resource/pubmed/chemical/Dizocilpine Maleate,
http://linkedlifedata.com/resource/pubmed/chemical/Ketamine,
http://linkedlifedata.com/resource/pubmed/chemical/N-Methylaspartate,
http://linkedlifedata.com/resource/pubmed/chemical/Phencyclidine
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0022-3565
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
245
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
969-74
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2838610-Anesthesia,
pubmed-meshheading:2838610-Animals,
pubmed-meshheading:2838610-Anticonvulsants,
pubmed-meshheading:2838610-Aspartic Acid,
pubmed-meshheading:2838610-Behavior, Animal,
pubmed-meshheading:2838610-Catalepsy,
pubmed-meshheading:2838610-Columbidae,
pubmed-meshheading:2838610-Dibenzocycloheptenes,
pubmed-meshheading:2838610-Discrimination Learning,
pubmed-meshheading:2838610-Dizocilpine Maleate,
pubmed-meshheading:2838610-Ketamine,
pubmed-meshheading:2838610-Macaca mulatta,
pubmed-meshheading:2838610-Male,
pubmed-meshheading:2838610-N-Methylaspartate,
pubmed-meshheading:2838610-Phencyclidine,
pubmed-meshheading:2838610-Rats,
pubmed-meshheading:2838610-Rats, Inbred Strains,
pubmed-meshheading:2838610-Self Administration,
pubmed-meshheading:2838610-Synaptic Transmission
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pubmed:year |
1988
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pubmed:articleTitle |
MK-801, a proposed noncompetitive antagonist of excitatory amino acid neurotransmission, produces phencyclidine-like behavioral effects in pigeons, rats and rhesus monkeys.
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pubmed:affiliation |
Department of Pharmacology, University of Michigan, Ann Arbor.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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