The effect of a new water-soluble sedative-hypnotic drug, JM-1232(-), on long-term potentiation in the CA1 region of the mouse hippocampus

Anesthesia and Analgesia

Volumn 113, Issue 5, 2011, Pages 1043-1049

  Takamatsu, Isao ^a   Sekiguchi, Masayuki ^a   Yonamine, Ryuji ^a   Wada, Keiji ^a   Kazama, Tomiei ^b  

^a NATIONAL DEFENSE MEDICAL COLLEGE   (Japan)

^b NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

3 [2 (4 METHYL 1 PIPERAZINYL) 2 OXOETHYL] 2 PHENYL 3,5,6,7 TETRAHYDROCYCLOPENTA[F]ISOINDOL 1(2H)ONE; 6 CYANO 7 NITRO 2,3 QUINOXALINEDIONE; DIZOCILPINE; FLUMAZENIL; HYPNOTIC SEDATIVE AGENT; JM 1232; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; DRUG BINDING SITE; DRUG MECHANISM; DRUG SOLUBILITY; EXCITATORY POSTSYNAPTIC POTENTIAL; HIPPOCAMPAL CA1 REGION; INHIBITORY POSTSYNAPTIC POTENTIAL; LONG TERM POTENTIATION; MALE; MOUSE; NERVE CELL PLASTICITY; NONHUMAN; PRIORITY JOURNAL; PYRAMIDAL NERVE CELL; SYNAPTIC TRANSMISSION;

EID: 80055097094     PISSN: 00032999     EISSN: None     Source Type: Journal    
DOI: 10.1213/ANE.0b013e3182291782     Document Type: Article

References (1)

1. Orser BA, Bertlik M, Wang LY, MacDonald JF. Inhibition by propofol (2,6 di-isopropylphenol) of the N-methyl-D-aspartate subtype of glutamate receptor in cultured hippocampal neurones. Br J Pharmacol 1995;116:1761-8