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The Journal of Neurophysiology Vol. 87 No. 4 April 2002, pp. 1790-1798
Copyright ©2002 by the American Physiological Society
Sleep Research Laboratory, Program in Behavioral Neuroscience and Department of Psychiatry, Boston University School of Medicine, Boston, Massachusetts 02118
Datta, Subimal
Evidence That REM Sleep Is Controlled by the Activation of Brain
Stem Pedunculopontine Tegmental Kainate Receptor. J. Neurophysiol. 87: 1790-1798, 2002. Glutamate, the
neurotransmitter, enhances rapid-eye-movement (REM) sleep when
microinjected into the brain stem pedunculopontine tegmentum (PPT) of
the cat and rat. Glutamate and its various receptors are normally
present in the PPT cholinergic cell compartment. The aim of this study
was to identify which specific receptor(s) in the cholinergic cell
compartment of the PPT are involved in glutamate-induced-REM sleep. To
identify these glutamate-induced REM-sleep-generating receptor(s) in
the PPT cholinergic cell compartment, specific receptors were
pharmacologically blocked differentially by localized pretreatment of
specific glutamate receptor antagonists; glutamate was then
microinjected into the PPT cholinergic cell compartment while
quantifying the effects on REM sleep in freely moving chronically
instrumented rats. The results demonstrate that when kainate receptors
were blocked by pretreatment with a kainate-specific receptor
antagonist, microinjection of glutamate was unable to induce REM sleep.
Pharmacological blockade of specific N-methyl-D-aspartate and
-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors was
unable to block glutamate-microinjection-induced-REM sleep. These
findings suggest, for the first time, that the activation of kainate
receptors within the cholinergic cell compartment of the PPT is an
essential portion of the mechanism for the generation of
glutamate-induced REM sleep in the rat.
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