NSAID zaltoprofen possesses novel anti-nociceptive mechanism through blockage of B2-type bradykinin receptor in nerve endings

Neuroscience Letters

Volumn 397, Issue 3, 2006, Pages 249-253

  Matsumoto, Misaki ^a   Inoue, Makoto ^a   Ueda, Hiroshi ^a  

^a NAGASAKI UNIVERSITY   (Japan)

Author keywords

B2 type BK receptor; Bradykinin; NSAID; Zaltoprofen

Indexed keywords

1 [[6 (3 METHOXYESTRA 1,3,5(10) TRIEN 17BETA YL)AMINO]HEXYL] 1H PYRROLE 2,5 DIONE; 1 [[6 (3 METHOXYESTRA 1,3,5(10) TRIEN 17BETA YL)AMINO]HEXYL] 2,5 PYRROLIDINEDIONE; BRADYKININ; BRADYKININ B2 RECEPTOR; LOXOPROFEN; NONSTEROID ANTIINFLAMMATORY AGENT; PROPIONIC ACID DERIVATIVE; ZALTOPROFEN;

ANALGESIA; ANIMAL EXPERIMENT; ANTINOCICEPTION; ARTICLE; CONTROLLED STUDY; DRUG INHIBITION; EXPERIMENTAL ANIMAL; FLEXOR REFLEX; MALE; MOUSE; NERVE ENDING; NONHUMAN; PRIORITY JOURNAL; RECEPTOR BLOCKING;

ANALGESICS; ANIMALS; ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; BENZOPYRANS; MALE; MICE; NERVE ENDINGS; PAIN; PAIN MEASUREMENT; PROPIONIC ACIDS; RECEPTOR, BRADYKININ B2; SCIATIC NERVE; SUBSTANCE P;

EID: 33644972845     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2005.12.037     Document Type: Article

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