2 DISTINCT GLUTAMATERGIC SYNAPTIC INPUTS TO STRIATAL MEDIUM SPINY NEURONS OF NEONATAL RATS AND PAIRED-PULSE DEPRESSION
Citation
A. Mori et al., 2 DISTINCT GLUTAMATERGIC SYNAPTIC INPUTS TO STRIATAL MEDIUM SPINY NEURONS OF NEONATAL RATS AND PAIRED-PULSE DEPRESSION, Journal of physiology, 476(2), 1994, pp. 217-228
Categorie Soggetti
Physiology
SICI code
0022-3751(1994)476:2<217:2DGSIT>2.0.ZU;2-Q
Abstract
1. Excitatory postsynaptic currents (EPSCs) were recorded from the med
ium spiny neurones of neonatal rat striatal slices using the whole-cel
l patch clamp method. EPSCs were selectively elicited in the presence
of picrotoxin with a glass stimulating pipette placed in the striatum.
2. We found two distinct unitary EPSCs that were evoked by stimulatio
n of single presynaptic fibres. The major type of EPSC, termed 'S-type
', failed frequently and had a small mean amplitude (2. 05 pA). They p
robably represented cortical afferents. 3. The other type of unitary E
PSC, the 'H-type', seldom failed and was 13 times larger than the S-ty
pe. Spontaneous EPSCs with amplitudes similar to those of H-type EPSCs
could be induced. 4. H-type EPSCs were mediated by both non-NMDA and
NMDA receptors. 5. The two types of EPSCs could be evoked in the same
neurones. The intensity of stimulation for H-type EPSCs was higher tha
n that for S-type EPSCs. 6. H-type EPSCs could be polysynaptically act
ivated, suggesting the presence of glutamatergic interneurones in the
striatum that generated H-type EPSCs. 7. H-type EPSCs displayed partic
ularly long-lasting paired-pulse depression, while that displayed by t
he S-type EPSCs was short. The paired-pulse depression of both EPSCs w
as Ca2+ dependent and involved presynaptic mechanisms. 8. We have demo
nstrated that the medium spiny neurones of neonatal rats receive two d
ifferent glutamatergic input systems having different amplitudes, orig
ins and paired pulse depression, reminiscent of cerebellar Purkinje ce
lls. This suggests that the two types of EPSCs also play distinctive r
oles in striatal neuronal circuitry.