Literature DB >> 11172778

GABAergic neurons of the laterodorsal and pedunculopontine tegmental nuclei of the cat express c-fos during carbachol-induced active sleep.

P Torterolo1, J Yamuy, S Sampogna, F R Morales, M H Chase.   

Abstract

The laterodorsal and pedunculopontine tegmental nuclei (LDT-PPT) are involved in the generation of active sleep (AS; also called REM or rapid eye movement sleep). Although the LDT-PPT are composed principally of cholinergic neurons that participate in the control of sleep and waking states, the function of the large number of GABAergic neurons that are also located in the LDT-PPT is unknown. Consequently, we sought to determine if these neurons are activated (as indicated by their c-fos expression) during active sleep induced by the microinjection of carbachol into the rostro-dorsal pons (AS-carbachol). Accordingly, immunocytochemical double-labeling techniques were used to identify GABA and Fos protein, as well as choline acetyltransferase (ChAT), in histological sections of the LDT-PPT. Compared to control awake cats, there was a larger number of GABAergic neurons that expressed c-fos during AS-carbachol (31.5+/-6.1 vs. 112+/-15.2, P<0.005). This increase in the number of GABA+Fos+ neurons occurred on the ipsilateral side relative to the injection site; there was a small decrease in GABA+Fos+ cells in the contralateral LDT-PPT. However, the LDT-PPT neurons that exhibited the largest increase in c-fos expression during AS-carbachol were neither GABA+ nor ChAT+ (47+/-22.5 vs. 228.7+/-14.0, P<0.0005). The number of cholinergic neurons that expressed c-fos during AS-carbachol was not significantly different compared to wakefulness. These data demonstrate that, during AS-carbachol, GABAergic as well as an unidentified population of neurons are activated in the LDT-PPT. We propose that these non-cholinergic LDT-PPT neurons may participate in the regulation of active sleep.

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Year:  2001        PMID: 11172778     DOI: 10.1016/s0006-8993(00)03264-9

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  13 in total

1.  Selective activation of the extended ventrolateral preoptic nucleus during rapid eye movement sleep.

Authors:  Jun Lu; Alvhild A Bjorkum; Man Xu; Stephanie E Gaus; Priyattam J Shiromani; Clifford B Saper
Journal:  J Neurosci       Date:  2002-06-01       Impact factor: 6.167

2.  GABAergic modulation of developing pedunculopontine nucleus.

Authors:  Kevin D Bay; Paige Beck; Robert D Skinner; Edgar Garcia-Rill
Journal:  Neuroreport       Date:  2007-02-12       Impact factor: 1.837

3.  Characterization of GABAergic neurons in rapid-eye-movement sleep controlling regions of the brainstem reticular formation in GAD67-green fluorescent protein knock-in mice.

Authors:  Ritchie E Brown; James T McKenna; Stuart Winston; Radhika Basheer; Yuchio Yanagawa; Mahesh M Thakkar; Robert W McCarley
Journal:  Eur J Neurosci       Date:  2008-01       Impact factor: 3.386

Review 4.  Neurosteroids and cholinergic systems: implications for sleep and cognitive processes and potential role of age-related changes.

Authors:  Olivier George; Monique Vallée; Michel Le Moal; Willy Mayo
Journal:  Psychopharmacology (Berl)       Date:  2006-01-17       Impact factor: 4.530

Review 5.  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

6.  A restricted parabrachial pontine region is active during non-rapid eye movement sleep.

Authors:  P Torterolo; S Sampogna; M H Chase
Journal:  Neuroscience       Date:  2011-06-15       Impact factor: 3.590

7.  The role of mesopontine NGF in sleep and wakefulness.

Authors:  Oscar V Ramos; Pablo Torterolo; Vincent Lim; Michael H Chase; Sharon Sampogna; Jack Yamuy
Journal:  Brain Res       Date:  2011-07-12       Impact factor: 3.252

8.  Endogenous GABA levels in the pontine reticular formation are greater during wakefulness than during rapid eye movement sleep.

Authors:  Giancarlo Vanini; Bradley L Wathen; Ralph Lydic; Helen A Baghdoyan
Journal:  J Neurosci       Date:  2011-02-16       Impact factor: 6.167

9.  Identification of cholinergic and non-cholinergic neurons in the pons expressing phosphorylated cyclic adenosine monophosphate response element-binding protein as a function of rapid eye movement sleep.

Authors:  S Datta; D F Siwek; E C Stack
Journal:  Neuroscience       Date:  2009-06-18       Impact factor: 3.590

Review 10.  Sleep-Wake Neurobiology.

Authors:  Giancarlo Vanini; Pablo Torterolo
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

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