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The Journal of Neuroscience, October 15, 2001, 21(20):8145-8153
Excitatory and Inhibitory Circuitry in the Superficial Gray Layer
of the Superior Colliculus
Psyche H.
Lee1,
Matthias
Schmidt1, 2, and
William C.
Hall1
1 Department of Neurobiology, Duke University Medical
Center, Durham, North Carolina 27710, and 2 Department of
Zoology and Neurobiology, Ruhr-University, D-44780 Bochum, Germany
Stratum griseum superficiale (SGS) of the superior colliculus
receives a dense cholinergic input from the parabigeminal nucleus. In
this study, we examined in vitro the modulatory
influence of acetylcholine (ACh) on the responses of SGS neurons that
project to the visual thalamus in the rat. We used whole-cell
patch-clamp recording to measure the responses of these projection
neurons to electrical stimulation of their afferents in the stratum
opticum (SO) before and during local pressure injections of ACh. These colliculothalamic projection neurons (CTNs) were identified during the
in vitro experiments by prelabeling them from the
thalamus with the retrograde axonal tracer wheat germ
agglutinin-apo-HRP-gold. In a group of cells that included the
prelabeled neurons, EPSCs evoked by SO stimulation were
significantly reduced by the application of ACh, whereas IPSC
amplitudes were significantly enhanced. Similar effects were observed
when the nicotinic ACh receptor agonist lobeline was used. Application
of the selective GABAB receptor antagonist
3-[[(3,4-dichlorophenyl)-methyl]amino]propyl](diethoxymethyl)phosphinic acid blocked ACh-induced reduction in the evoked response. In contrast, the ACh-induced reduction was insensitive to application of
the GABAA receptor antagonist bicuculline. The ACh-induced reduction was also diminished by bath application of muscimol at the
low concentrations that selectively activate
GABAC receptors. Because GABAC receptors may be
specifically expressed by GABAergic SGS interneurons (Schmidt et al.,
2001), our results support the hypothesis that ACh reduces CTN activity
by nicotinic receptor-mediated excitation of local GABAergic
interneurons. These interneurons in turn use GABAB
receptors to inhibit the CTNs.
Key words:
acetylcholine; nicotinic ACh receptors; muscarinic ACh
receptors; cholinergic circuits; interneurons; patch clamp; superior
colliculus
Copyright © 2001 Society for Neuroscience 0270-6474/01/21208145-09$05.00/0
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