Literature DB >> 11377848

Interactions between cholinergic and GABAergic neurotransmitters in and around the locus coeruleus for the induction and maintenance of rapid eye movement sleep in rats.

B N Mallick1, S Kaur, R N Saxena.   

Abstract

The noradrenergic "REM-off" neurons in the locus coeruleus cease firing, whereas some cholinergic and non-cholinergic "REM-on" neurons increase firing during rapid eye movement sleep. A reciprocal interaction between these neurons was proposed. However, acetylcholine did not inhibit neurons in the locus coeruleus. Nevertheless, since GABA levels increase during rapid eye movement sleep and picrotoxin injections into the locus coeruleus reduced rapid eye movement sleep, it was hypothesized that GABA in the locus coeruleus might play an intermediary inhibitory role for rapid eye movement sleep regulation. Therefore, the effects of GABA or carbachol (a mixed cholinergic agonist receptor) alone, as well as an agonist of one in presence of an antagonist of the other, in the locus coeruleus were investigated on sleep-wakefulness and rapid eye movement sleep. The cholinergic agonist carbachol increased, while the muscarinic antagonist receptor scopolamine decreased, the frequency of induction of rapid eye movement sleep per hour. In contrast, GABA and picrotoxin increased and decreased, respectively, the duration of rapid eye movement sleep per episode. However, when carbachol was injected in the presence of picrotoxin or GABA was injected in the presence of scopolamine, the effect of GABA or picrotoxin was dominant. Microinjection of both scopolamine and picrotoxin in combination reduced both the frequency of initiation as well as the duration per episode of rapid eye movement sleep. From these results we suggest that in the locus coeruleus cholinergic input modulates the frequency of induction of rapid eye movement sleep and this action is mediated through GABA interneurons, whereas the length of rapid eye movement sleep per episode is maintained by the presence of an optimum level of GABA. A model of neural connections for initiation and maintenance of rapid eye movement sleep is proposed and discussed.

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Year:  2001        PMID: 11377848     DOI: 10.1016/s0306-4522(01)00062-8

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  16 in total

Review 1.  Role of norepinephrine in the regulation of rapid eye movement sleep.

Authors:  Birendra N Mallick; Sudipta Majumdar; Mohd Faisal; Vikas Yadav; Vibha Madan; Dinesh Pal
Journal:  J Biosci       Date:  2002-09       Impact factor: 1.826

2.  Dynamics of neuron spike activity in the oral nucleus of the pons during the sleep-waking cycle in cats.

Authors:  O Yu Dergacheva; I E Khachikova; A A Burikov
Journal:  Neurosci Behav Physiol       Date:  2004-06

Review 3.  Mechanism of noradrenaline-induced stimulation of Na-K ATPase activity in the rat brain: implications on REM sleep deprivation-induced increase in brain excitability.

Authors:  Birendra Nath Mallick; Sudhuman Singh; Abhishek Singh
Journal:  Mol Cell Biochem       Date:  2009-10-13       Impact factor: 3.396

4.  Sleep duration varies as a function of glutamate and GABA in rat pontine reticular formation.

Authors:  Christopher J Watson; Ralph Lydic; Helen A Baghdoyan
Journal:  J Neurochem       Date:  2011-07-01       Impact factor: 5.372

Review 5.  REM sleep: a biological and psychological paradox.

Authors:  Jerome M Siegel
Journal:  Sleep Med Rev       Date:  2011-04-08       Impact factor: 11.609

6.  A Moderate Increase of Physiological CO(2) in a Critical Range during Stable NREM Sleep Episode: A Potential Gateway to REM Sleep.

Authors:  Vibha Madan; Sushil K Jha
Journal:  Front Neurol       Date:  2012-02-20       Impact factor: 4.003

7.  Rapid eye movements during sleep in mice: high trait-like stability qualifies rapid eye movement density for characterization of phenotypic variation in sleep patterns of rodents.

Authors:  Stephany Fulda; Christoph P N Romanowski; Andreas Becker; Thomas C Wetter; Mayumi Kimura; Thomas Fenzel
Journal:  BMC Neurosci       Date:  2011-11-02       Impact factor: 3.288

8.  Rapid Eye Movement Sleep Deprivation Induces Neuronal Apoptosis by Noradrenaline Acting on Alpha1 Adrenoceptor and by Triggering Mitochondrial Intrinsic Pathway.

Authors:  Bindu I Somarajan; Mudasir A Khanday; Birendra N Mallick
Journal:  Front Neurol       Date:  2016-03-07       Impact factor: 4.003

9.  A mathematical model towards understanding the mechanism of neuronal regulation of wake-NREMS-REMS states.

Authors:  Rupesh Kumar; Amitabha Bose; Birendra Nath Mallick
Journal:  PLoS One       Date:  2012-08-08       Impact factor: 3.240

10.  Local properties of vigilance states: EMD analysis of EEG signals during sleep-waking states of freely moving rats.

Authors:  Rupesh Kumar; Ram Ramaswamy; Birendra Nath Mallick
Journal:  PLoS One       Date:  2013-10-22       Impact factor: 3.240

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