Literature DB >> 18308473

Role of the dorsal paragigantocellular reticular nucleus in paradoxical (rapid eye movement) sleep generation: a combined electrophysiological and anatomical study in the rat.

R Goutagny1, P-H Luppi, D Salvert, D Lapray, D Gervasoni, P Fort.   

Abstract

It is well known that noradrenergic locus coeruleus neurons decrease their activity during slow wave sleep and are quiescent during paradoxical sleep. It was recently proposed that their inactivation during paradoxical sleep is due to a tonic GABAergic inhibition arising from neurons located into the dorsal paragigantocellular reticular nucleus (DPGi). However, the discharge profile of DPGi neurons across the sleep-waking cycle as well as their connections with brain areas involved in paradoxical sleep regulation remain to be described. Here we show, for the first time in the unanesthetized rat that the DPGi contained a subtype of neurons with a tonic and sustained firing activation specifically during paradoxical sleep (PS-on neurons). Noteworthy, their firing rate increase anticipated for few seconds the beginning of the paradoxical sleep bout. By using anterograde tract-tracing, we further showed that the DPGi, in addition to locus coeruleus, directly projected to other areas containing wake-promoting neurons such as the serotonergic neurons of the dorsal raphe nucleus and hypocretinergic neurons of the posterior hypothalamus. Finally, the DPGi sent efferents to the ventrolateral part of the periaqueductal gray matter known to contain paradoxical sleep-suppressing neurons. Taken together, our original results suggest that the PS-on neurons of the DPGi may have their major role in simultaneous inhibitory control over the wake-promoting neurons and the permissive ventrolateral part of the periaqueductal gray matter as a means of influencing vigilance states and especially PS generation.

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Year:  2007        PMID: 18308473     DOI: 10.1016/j.neuroscience.2007.12.014

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


  25 in total

Review 1.  Brainstem mechanisms of paradoxical (REM) sleep generation.

Authors:  Pierre-Hervé Luppi; Olivier Clement; Emilie Sapin; Christelle Peyron; Damien Gervasoni; Lucienne Léger; Patrice Fort
Journal:  Pflugers Arch       Date:  2011-11-15       Impact factor: 3.657

2.  In the flicker of an eye.

Authors:  N P Pedersen; P M Fuller; J Lu; C B Saper
Journal:  J Physiol       Date:  2008-07-15       Impact factor: 5.182

3.  Confirmation of the consensus that glycinergic postsynaptic inhibition is responsible for the atonia of REM sleep.

Authors:  Michael H Chase
Journal:  Sleep       Date:  2008-11       Impact factor: 5.849

Review 4.  Control of sleep and wakefulness.

Authors:  Ritchie E Brown; Radhika Basheer; James T McKenna; Robert E Strecker; Robert W McCarley
Journal:  Physiol Rev       Date:  2012-07       Impact factor: 37.312

5.  Evidence that neurons of the sublaterodorsal tegmental nucleus triggering paradoxical (REM) sleep are glutamatergic.

Authors:  Olivier Clément; Emilie Sapin; Anne Bérod; Patrice Fort; Pierre-Hervé Luppi
Journal:  Sleep       Date:  2011-04-01       Impact factor: 5.849

Review 6.  Neural Control of the Upper Airway: Respiratory and State-Dependent Mechanisms.

Authors:  Leszek Kubin
Journal:  Compr Physiol       Date:  2016-09-15       Impact factor: 9.090

Review 7.  Neural Circuitry of Wakefulness and Sleep.

Authors:  Thomas E Scammell; Elda Arrigoni; Jonathan O Lipton
Journal:  Neuron       Date:  2017-02-22       Impact factor: 17.173

8.  Medullary circuitry regulating rapid eye movement sleep and motor atonia.

Authors:  Ramalingam Vetrivelan; Patrick M Fuller; Qingchun Tong; Jun Lu
Journal:  J Neurosci       Date:  2009-07-22       Impact factor: 6.167

Review 9.  The anatomical, cellular and synaptic basis of motor atonia during rapid eye movement sleep.

Authors:  Elda Arrigoni; Michael C Chen; Patrick M Fuller
Journal:  J Physiol       Date:  2016-07-03       Impact factor: 5.182

10.  GABAergic antagonism of the central nucleus of the amygdala attenuates reductions in rapid eye movement sleep after inescapable footshock stress.

Authors:  Xianling Liu; Linghui Yang; Laurie L Wellman; Xiangdong Tang; Larry D Sanford
Journal:  Sleep       Date:  2009-07       Impact factor: 5.849

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