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The Journal of Neurophysiology Vol. 87 No. 4 April 2002, pp. 2124-2136
Copyright ©2002 by the American Physiological Society
Section of Neurobiology, Yale University School of Medicine, New Haven, Connecticut 06510
Monckton, James E. and
David A. McCormick.
Neuromodulatory Role of Serotonin in the Ferret Thalamus. J. Neurophysiol. 87: 2124-2136, 2002. Serotonergic fibers broadly innervate the thalamus and may
influence the sleep wake cycle, attention, and other processes through
modulation of neurons in this structure. However, the actions of
serotonin in the dorsal thalamus have been investigated in detail only
in the dorsal lateral geniculate nucleus. In the present study, we
examined the action of serotonin in several different regions of the
ferret dorsal thalamus, including the associative nuclei, using the in
vitro slice preparation and intracellular recording techniques. In
nearly all nuclei examined, the predominant action of serotonin was one
of hyperpolarization and inhibition of the tonic firing mode. The
magnitude of the hyperpolarizing response decreased with age and varied
greatly across and somewhat within nuclei maintaining the following
relationship (in descending order of magnitude): lateral posterior,
lateral dorsal, pulvinar, mediodorsal, center median, anteroventral,
central lateral, ventral basal, and medial geniculate. This
hyperpolarization is elicited through two mechanisms: one direct and
the other via local interneurons. The direct action occurs through an
increase in potassium conductance mediated through the
5-HT1A receptor. This conclusion is supported by
the findings that it persists in the presence of tetrodotoxin and block
of GABAergic synaptic transmission, the reversal potential shifts in a
Nernstian fashion with changes in extracellular potassium concentration, and the response is antagonized by the
5-HT1A antagonist WAY100635 and mimicked by the
application of the 5-HT1A-selective agonist 8-OH
DPAT. The second mechanism by which 5-HT evoked a hyperpolarization was
through the activation of local interneurons. In slices in which GABA
receptors were not blocked, 5-HT application increased the frequency
and amplitude of spontaneous inhibitory postsynaptic potentials (IPSPs)
occurring in thalamocortical neurons. Application of 5-HT to
physiologically or morphologically identified interneurons evoked a
prolonged suprathreshold depolarization. Our results suggest that
serotonergic inputs act differentially across the thalamus in a complex
manner involving direct and indirect mechanisms. It appears that 5-HT
has a greater direct postsynaptic inhibitory influence in the
posterior, medial, and intralaminar nuclei than in the primary sensory nuclei.
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