Abstract
Orexins are important regulators of sleep-wakefulness (S-W). Rats were intracerebroventricularly (ICV) administered selective orexin-2 receptor antagonist, TCS-OX2-29. There was decreased wakefulness due to a decrease in the average wake episode duration and an increased REM sleep due to an increase in the number of REM episodes, indicating an inhibitory role of the central orexin-2 receptors on REM sleep generation.
Copyright © 2012 Elsevier B.V. All rights reserved.
MeSH terms
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Animals
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Injections, Intraventricular
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Isoquinolines / administration & dosage*
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Male
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Orexin Receptors
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Pyridines / administration & dosage*
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Rats
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Rats, Sprague-Dawley
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Rats, Wistar
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Receptors, G-Protein-Coupled / antagonists & inhibitors*
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Receptors, G-Protein-Coupled / metabolism
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Receptors, Neuropeptide / antagonists & inhibitors*
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Receptors, Neuropeptide / metabolism
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Sleep, REM / drug effects*
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Time Factors
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Wakefulness / drug effects
Substances
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1-(3,4-dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)-3,3-dimethyl-2-((4-pyridinylmethyl)amino)-1-butanone
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Isoquinolines
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Orexin Receptors
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Pyridines
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Receptors, G-Protein-Coupled
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Receptors, Neuropeptide