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Volume 17, Number 22,
Issue of November 15, 1997
pp. 8880-8893
Functional Properties of Perigeniculate Inhibition of Dorsal
Lateral Geniculate Nucleus Thalamocortical Neurons In
Vitro
Received June 17, 1997; revised Aug. 4, 1997; accepted Aug. 28, 1997.
Maria V. Sanchez-Vives and
David A. McCormick
Section of Neurobiology, Yale University School of Medicine, New
Haven, Connecticut 06510
The properties of the inhibitory influence of neurons in the
perigeniculate (PGN) nucleus on thalamocortical cells were examined with intracellular recordings in the ferret geniculate slice maintained in vitro. Activation of PGN neurons with the local
application of glutamate caused IPSPs in thalamocortical neurons that
were mediated by both GABAA and GABAB
receptors, as well as the activation of spindle waves.
With low intensity stimulation of the PGN, local application of
bicuculline to the dorsal lateral geniculate nucleus (LGNd) strongly
inhibited evoked and spindle-associated IPSPs, indicating that these
are largely mediated by GABAA receptors. The generation of
GABAB receptor-mediated IPSPs in thalamocortical cells that were large enough to generate rebound low threshold
Ca2+ spikes required substantially increased
activation of the PGN with glutamate.
The activation of synchronous bicuculline-induced slowed oscillations
in thalamocortical neurons required the block of GABAA receptors in the LGNd as well as in the PGN. These results indicate that bursts of action potentials in PGN neurons can result in the
activation of both GABAA and GABAB receptors in
thalamocortical neurons, with the strong activation of
GABAB receptors requiring an intense, simultaneous
discharge of a number of PGN neurons. Functionally, these results
suggest that PGN neurons inhibit thalamocortical cells preferentially
through the activation of GABAA receptors, although the
strong activation of GABAB receptors may occur under pathological conditions and contribute to the generation of abnormal, synchronous slow oscillations.
Key words:
inhibition;
thalamus;
sleep;
thalamic reticular nucleus;
GABAergic;
oscillations
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