M. Salami et al., Effects of ketamine on synaptic transmission and long-term potentiation inlayer II/III of rat visual cortex in vitro, EUR J PHARM, 390(3), 2000, pp. 287-293
The effects of ketamine, which has NMDA receptor antagonist properties, on
synaptic transmission and long-term potentiation in layer II/III of adult r
at visual cortex were examined in vitro. Field potentials were recorded in
layer II/III following layer IV stimulation. Primed-burst stimulation was u
sed for induction of long-term potentiation. Stimulation of layer IV result
ed in a two-component response in layer II/III, a population excitatory pos
tsynaptic potential1 (EPSP1) and a population excitatory postsynaptic poten
tial2 (EPSP2). DL-2-Amino-5-phosphono-valeric acid (AP5), a competitive NMD
A receptor antagonist, reduced the amplitude of the population EPSP1 while
ketamine increased the amplitude of the population EPSP2. The results showe
d that primed-burst stimulation induced long-term potentiation in layer II/
III of the visual cortex in vitro. Preincubation for 30 min with AP5 (25-10
0 mu M) reduced the extent of long-term potentiation of the population EPSP
2 and blocked the induction of long-term potentiation of the population EPS
P1. When ketamine (100-200 mu M) was present for 30 min prior to tetanic st
imulation, it blocked the induction of long-term potentiation of the popula
tion EPSP1 and reduced the extent of long-term potentiation of the populati
on EPSP2. We conclude that ketamine can interfere with synaptic transmissio
n in the visual cortex. Primed-burst stimulation is an effective protocol f
or neocortical potentiation. NMDA receptors are involved in the induction o
f long-term potentiation by primed-burst stimulation of the population EPSP
1 and population EPSP2 in adult rat visual cortex in vitro. (C) 2000 Elsevi
er Science B.V. all rights reserved.