Literature DB >> 9881870

A key role for the caudoventral pontine tegmentum in the simultaneous generation of eye saccades in bursts and associated ponto-geniculo-occipital waves during paradoxical sleep in the cat.

G Vanni-Mercier1, G Debilly.   

Abstract

Ponto-geniculo-occipital waves and rapid eye movements (eye saccades) are two prominent phasic events of paradoxical sleep which occur in conjunction. Although they have been studied intensively, the neuronal link between these two events is still poorly understood. On the basis of our previous results, combining brainstem transections and carbachol microinjections, we postulated that the oculomotor and ponto-geniculo-occipital systems do not work in series, but in parallel, and that the caudoventral pontine tegmentum might represent a structure controlling and/or co-ordinating the simultaneous production of the two phenomena. This hypothesis was further supported by the demonstration that, during paradoxical sleep, the instantaneous velocity of eye saccades in bursts is higher than that of isolated ones which, in turn, are more rapid than waking saccades. This acceleration of eye saccades in bursts also seems to be under the cholinergic control of the caudoventral pontine tegmentum. In order to test the hypothesis that this area may be a prime mover leading to the simultaneous appearance of these two phasic events as a whole, we investigated, in the present study, the effects of pharmacological stimulation (with carbachol) and inhibition (with atropine) of the caudoventral pontine tegmentum on the production and the characteristics of eye saccades and ponto-geniculo-occipital waves. Cats' eye movements were recorded using the technique of the scleral search coil in a magnetic field, together with sleep-waking parameters. We found that: (i) unilateral microinjections of carbachol (0.4 microg) induced, during waking, a majority of long bursts of ponto-geniculo-occipital waves (i.e. bursts containing at least five waves) which had intra-burst intervals similar to natural ones (48-259 ms) and decreased the frequency of isolated ponto-geniculo-occipital waves; (ii) unilateral microinjections of atropine (2.4 microg) strongly decreased, during paradoxical sleep, the frequency (number/min) of eye saccades in bursts directed contralaterally to the side of the injection (by 48-54%) and reduced the velocity of these saccades to that of isolated eye saccades. Atropine also significantly reduced the frequency (by 60%) of all types of bursts of ponto-geniculo-occipital waves, with a maximal effect (80% reduction) on long bursts of ponto-geniculo-occipital waves, while it increased the frequency of isolated ponto-geniculo-occipital waves. However, atropine did not change the value of intra-burst intervals. These findings support the hypothesis that eye saccades in bursts and associated ponto-geniculo-occipital waves are generated as a whole by a common structure and that this structure is at least partly defined by the caudoventral pontine tegmentum.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9881870     DOI: 10.1016/s0306-4522(98)00045-1

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


  13 in total

1.  Eye movements and abducens motoneuron behavior after cholinergic activation of the nucleus reticularis pontis caudalis.

Authors:  Javier Márquez-Ruiz; Miguel Escudero
Journal:  Sleep       Date:  2010-11       Impact factor: 5.849

2.  Tonic and phasic phenomena underlying eye movements during sleep in the cat.

Authors:  Javier Márquez-Ruiz; Miguel Escudero
Journal:  J Physiol       Date:  2008-05-22       Impact factor: 5.182

Review 3.  The developmental decrease in REM sleep: the role of transmitters and electrical coupling.

Authors:  Edgar Garcia-Rill; Amanda Charlesworth; David Heister; Meijun Ye; Abdallah Hayar
Journal:  Sleep       Date:  2008-05       Impact factor: 5.849

4.  Evidence for Electrical Coupling in the SubCoeruleus (SubC) Nucleus.

Authors:  David S Heister; Abdallah Hayar; Amanda Charlesworth; Charlotte Yates; Yi-Hong Zhou; Edgar Garcia-Rill
Journal:  J Neurophysiol       Date:  2007-01-10       Impact factor: 2.714

5.  Phasic motor activity of respiratory and non-respiratory muscles in REM sleep.

Authors:  Jimmy J Fraigne; John M Orem
Journal:  Sleep       Date:  2011-04-01       Impact factor: 5.849

6.  Orexinergic projections to the cat midbrain mediate alternation of emotional behavioural states from locomotion to cataplexy.

Authors:  Kaoru Takakusaki; Kazumi Takahashi; Kazuya Saitoh; Hirofumi Harada; Toshikatsu Okumura; Yukihiko Kayama; Yoshimasa Koyama
Journal:  J Physiol       Date:  2005-08-25       Impact factor: 5.182

7.  Electrophysiological characterization of neurons in the dorsolateral pontine rapid-eye-movement sleep induction zone of the rat: Intrinsic membrane properties and responses to carbachol and orexins.

Authors:  R E Brown; S Winston; R Basheer; M M Thakkar; R W McCarley
Journal:  Neuroscience       Date:  2006-09-26       Impact factor: 3.590

8.  Evidence of subthalamic PGO-like waves during REM sleep in humans: a deep brain polysomnographic study.

Authors:  Julio Fernández-Mendoza; Beatriz Lozano; Fernando Seijo; Elena Santamarta-Liébana; Maria José Ramos-Platón; Antonio Vela-Bueno; Fernando Fernández-González
Journal:  Sleep       Date:  2009-09       Impact factor: 5.849

Review 9.  Oscillating circuitries in the sleeping brain.

Authors:  Antoine R Adamantidis; Carolina Gutierrez Herrera; Thomas C Gent
Journal:  Nat Rev Neurosci       Date:  2019-10-15       Impact factor: 34.870

Review 10.  How the brain decides what we see.

Authors:  John Smythies
Journal:  J R Soc Med       Date:  2005-01       Impact factor: 18.000

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.