J. Davies et al., PHARMACOLOGICAL CHARACTERIZATION OF EXCITATORY SYNAPTIC TRANSMISSION IN THE CAT RED NUCLEUS IN-VIVO, Brain research, 649(1-2), 1994, pp. 43-52
Extracellular recordings were made from the magnocellular neurones of
the red nucleus (mRN) in anaesthetised cats. A study was made of the e
ffects of selective excitatory amino acid receptor antagonists on exci
tatory monosynaptic responses evoked from the sensorimotor cortex (SMC
) and cerebellar interpositus nucleus (IPN). Iontophoretically applied
CNQX and NBQX antagonised both SMC and IPN responses whereas, D-AP5 i
nhibited the SMC response but was ineffective to the IPN. At currents
that selectively antagonised NMDA responses, CPPene had no effect on e
ither SMC or IPN responses. 7-chlorokynurenate inhibited both SMC and
IPN responses but required currents that antagonised both AMPA and NMD
A responses and was therefore acting in a non-selective manner. Iontop
horetically applied glycine was inhibitory to both agonist and synapti
c responses, whilst D-serine potentiated NMDA responses but did not en
hance monosynaptic responses of the SMC. However in the presence of ei
ther 7-chlorokynurenate or high currents of CNQX that reduced the SMC
synaptic activation of the mRN neurones, D-serine attenuated the inhib
itory action of these antagonists. It is concluded that monosynaptic r
esponses from the SMC are mediated by both NMDA and non-NMDA receptors
whereas the monosynaptic responses evoked from the IPN are mediated o
nly by non-NMDA receptors. The lack of effect of CPPene is consistent
with the postulate that two NMDA receptor subtypes are present on mRN
neurones.