Potentiation by DL-χ-aminopimelate of the inhibitory action of a novel mGluR agonist (L-F2CCG-I) on monosynaptic excitation in the rat spinal cord

British Journal of Pharmacology

Volumn 123, Issue 4, 1998, Pages 771-779

  Saitoh, T ^a   Ishida, M ^a   Shinozaki, H ^a  

^a TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

Author keywords

2 (carboxycyclopropyl)glycine (CCG); L F2CCG I; Metabotropic glutamate receptor; Monosynaptic reflexes; Potentiation; Priming; aminopimelate

Indexed keywords

2 (2 CARBOXY 3,3 DIFLUOROCYCLOPROPYL)GLYCINE; 2 AMINOPIMELIC ACID; 2-(2-CARBOXY-3,3-DIFLUOROCYCLOPROPYL)GLYCINE; ALPHA-AMINOPIMELIC ACID; AMINO ACID RECEPTOR STIMULATING AGENT; DICARBOXYLIC AMINO ACID; PIMELIC ACID DERIVATIVE;

ANIMAL; ARTICLE; CELL MEMBRANE POTENTIAL; CHEMISTRY; DRUG EFFECT; DRUG POTENTIATION; IN VITRO STUDY; PHYSIOLOGY; RAT; SPINAL CORD; STEREOISOMERISM; SYNAPSE; WISTAR RAT;

AMINO ACIDS, DICARBOXYLIC; ANIMALS; DRUG SYNERGISM; EXCITATORY AMINO ACID AGONISTS; MEMBRANE POTENTIALS; PIMELIC ACIDS; RATS; RATS, WISTAR; SPINAL CORD; STEREOISOMERISM; SYNAPSES;

EID: 0031992054     PISSN: 00071188     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.bjp.0701670     Document Type: Article

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