METABOTROPIC glutamate receptors (mGluRs) have been shown to contribut
e to nociceptive processing in the spinal cord. We have investigated t
he pharmacology of the mGluR agonist (1S,3R)-ACPD during inflammatory
hyperalgesia in an in vitro preparation of the juvenile rat hemisected
spinal cord. Superfusion of (1S,3R)-ACPD produced a concentration-dep
endent ventral root depolarization in naive and hyperalgesic animals w
ith no significant difference in EC50 values (55.5 +/- 6.36 mu M and 5
1.0 +/- 5.76 mu M, respectively, n = 4). However, the amplitude of the
maximum response was significantly enhanced by 23% in hyperalgesic co
mpared with naive animals. The NMDA receptor antagonist D-APS reversed
this effect, leaving the (1S,3R)-ACPD dose-response curve unchanged i
n naive animals. These results suggest a tonic NMDA component in the s
pinal cord during inflammatory hyperalgesia. (C) 1998 Rapid Science Lt
d.