Ifenprodil is known to inhibit channel opening of NMDA receptors containing
the NR2B subunit. However, it has also been shown to increase NMDA recepto
r affinity for glutamate-site agonists, including NMDA. The coexistence of
the two opposing effects may explain why ifenprodil can either enhance or s
uppress an NMDA response depending on the level of NMDA binding and thus th
e NMDA concentration. Using whole cell recordings in rat prefrontal cortica
l slices, we report here that the effect of ifenprodil also depends on the
speed and the direction of change of NMDA concentration. As shown previousl
y, ifenprodil increased the inward current induced by low concentrations of
NMDA applied through a local Y-tube perfusion system. However, the rising
phase of the current was less enhanced compared to the falling phase. Incre
asing the speed of rising of NMDA concentration further reduced the enhanci
ng effect of ifenprodil. When pressure ejection was used to produce even fa
ster NMDA responses, the entire rising phase including the peak of the resp
onse was suppressed by ifenprodil, while the falling phase remained enhance
d. These results are consistent with the suggestion that ifenprodil decreas
es both the association and dissociation rates of NMDA from NMDA receptors,
and suggest that, ifenprodil affects slow and fast NMDA responses in diffe
rent manners. In particular, this study suggests that ifenprodil inhibits t
he rising phase of a fast NMDA response by suppressing both channel opening
and the association of NMDA with NMDA receptors and that this inhibition c
an occur even when the level of NMDA binding is low. Synapse 39:313-318, 20
01. (C) 2001 Wiley-Liss, Inc.