Literature DB >> 23122879

Hypocretinergic and non-hypocretinergic projections from the hypothalamus to the REM sleep executive area of the pons.

Pablo Torterolo1, Sharon Sampogna, Michael H Chase.   

Abstract

Within the postero-lateral hypothalamus neurons that utilize hypocretin or melanin-concentrating hormone (MCH) as neuromodulators are co-distributed. These neurons have been involved in the control of behavioral states, and a deficit in the hypocretinergic system is the pathogenic basis of narcolepsy with cataplexy. In this report, utilizing immunohistochemistry and retrograde tracing techniques, we examined the hypocretinergic innervation of the nucleus pontis oralis (NPO), which is the executive site that is responsible for the generation of REM sleep in the cat. The retrograde tracer cholera toxin subunit b (CTb) was administered in pontine regions where carbachol microinjections induced REM sleep. Utilizing immunohistochemical techniques, we found that approximately 1% of hypocretinergic neurons in the tuberal area of the hypothalamus project to the NPO. In addition, approximately 6% of all CTb+ neurons in this region were hypocretinergic. The hypocretinergic innervation of the NPO was also compared with the innervation of the same site by MCH-containing neurons. More than three times as many MCHergic neurons were found to project to the NPO compared with hypocretinergic cells; both neuronal types exhibited bilateral projections. We also identified a group of non-hypocretinergic non-MCHergic neuronal group of neurons that were intermingled with both hypocretinergic and MCHergic neurons that also projected to this same brainstem region. These neurons were grater in number that either hypocretin or MCH-containing neurons; their soma size was also smaller and their projections were mainly ipsilateral. The present anatomical data suggest that hypocretinergic, MCHergic and an unidentified companion group of neurons of the postero-lateral hypothalamus participate in the regulation of the neuronal activity of NPO neurons, and therefore, are likely to participate in the control of wakefulness and REM sleep.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 23122879      PMCID: PMC3529971          DOI: 10.1016/j.brainres.2012.10.050

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


  58 in total

1.  Hypocretin receptor protein and mRNA expression in the dorsolateral pons of rats.

Authors:  M A Greco; P J Shiromani
Journal:  Brain Res Mol Brain Res       Date:  2001-03-31

2.  Anatomical demonstration of a medullary enkephalinergic pathway potentially implicated in the oro-facial muscle atonia of paradoxical sleep in the cat.

Authors:  P Fort; C Rampon; D Gervasoni; C Peyron; P H Luppi
Journal:  Sleep Res Online       Date:  1998

3.  Release of hypocretin (orexin) during waking and sleep states.

Authors:  Lyudmila I Kiyashchenko; Boris Y Mileykovskiy; Nigel Maidment; Hoa A Lam; Ming-Fung Wu; Joshi John; John Peever; Jerome M Siegel
Journal:  J Neurosci       Date:  2002-07-01       Impact factor: 6.167

4.  The injection of hypocretin-1 into the nucleus pontis oralis induces either active sleep or wakefulness depending on the behavioral state when it is administered.

Authors:  Mingchu Xi; Michael H Chase
Journal:  Sleep       Date:  2010-09       Impact factor: 5.849

Review 5.  The orexin system: roles in sleep/wake regulation.

Authors:  Takeshi Sakurai; Michihiro Mieda; Natsuko Tsujino
Journal:  Ann N Y Acad Sci       Date:  2010-07       Impact factor: 5.691

6.  Relationship between the perifornical hypothalamic area and oral pontine reticular nucleus in the rat. Possible implication of the hypocretinergic projection in the control of rapid eye movement sleep.

Authors:  A Nuñez; M E Moreno-Balandrán; M L Rodrigo-Angulo; M Garzón; I De Andrés
Journal:  Eur J Neurosci       Date:  2006-11-24       Impact factor: 3.386

7.  Induction of wakefulness and inhibition of active (REM) sleep by GABAergic processes in the nucleus pontis oralis.

Authors:  M C Xi; F R Morales; M H Chase
Journal:  Arch Ital Biol       Date:  2001-02       Impact factor: 1.000

8.  Sleep-wakefulness effects after microinjections of hypocretin 1 (orexin A) in cholinoceptive areas of the cat oral pontine tegmentum.

Authors:  Elena Moreno-Balandrán; Miguel Garzón; Cristina Bódalo; Fernando Reinoso-Suárez; Isabel de Andrés
Journal:  Eur J Neurosci       Date:  2008-07       Impact factor: 3.386

Review 9.  [Modulation by the hypocretinergic/orexinergic neurotransmission system in sleep-wakefulness cycle states].

Authors:  E del Cid-Pellitero; M Garzón
Journal:  Rev Neurol       Date:  2007 Oct 16-31       Impact factor: 0.870

10.  Presynaptic and postsynaptic actions and modulation of neuroendocrine neurons by a new hypothalamic peptide, hypocretin/orexin.

Authors:  A N van den Pol; X B Gao; K Obrietan; T S Kilduff; A B Belousov
Journal:  J Neurosci       Date:  1998-10-01       Impact factor: 6.167

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  7 in total

1.  Melanin-concentrating hormone neurons specifically promote rapid eye movement sleep in mice.

Authors:  Ramalingam Vetrivelan; Dong Kong; Loris L Ferrari; Elda Arrigoni; Joseph C Madara; Sathyajit S Bandaru; Bradford B Lowell; Jun Lu; Clifford B Saper
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2.  Optogenetic activation of melanin-concentrating hormone neurons increases non-rapid eye movement and rapid eye movement sleep during the night in rats.

Authors:  Carlos Blanco-Centurion; Meng Liu; Roda P Konadhode; Xiaobing Zhang; Dheeraj Pelluru; Anthony N van den Pol; Priyattam J Shiromani
Journal:  Eur J Neurosci       Date:  2016-10-16       Impact factor: 3.386

Review 3.  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

4.  The hypocretins (orexins) mediate the "phasic" components of REM sleep: A new hypothesis.

Authors:  Pablo Torterolo; Michael H Chase
Journal:  Sleep Sci       Date:  2014-08-20

5.  Synaptic interactions between perifornical lateral hypothalamic area, locus coeruleus nucleus and the oral pontine reticular nucleus are implicated in the stage succession during sleep-wakefulness cycle.

Authors:  Silvia Tortorella; Margarita L Rodrigo-Angulo; Angel Núñez; Miguel Garzón
Journal:  Front Neurosci       Date:  2013-11-19       Impact factor: 4.677

Review 6.  Melanin-Concentrating Hormone (MCH): Role in REM Sleep and Depression.

Authors:  Pablo Torterolo; Cecilia Scorza; Patricia Lagos; Jessika Urbanavicius; Luciana Benedetto; Claudia Pascovich; Ximena López-Hill; Michael H Chase; Jaime M Monti
Journal:  Front Neurosci       Date:  2015-12-17       Impact factor: 4.677

7.  Orexin signaling modulates synchronized excitation in the sublaterodorsal tegmental nucleus to stabilize REM sleep.

Authors:  Hui Feng; Si-Yi Wen; Qi-Cheng Qiao; Yu-Jie Pang; Sheng-Yun Wang; Hao-Yi Li; Jiao Cai; Kai-Xuan Zhang; Jing Chen; Zhi-An Hu; Fen-Lan Luo; Guan-Zhong Wang; Nian Yang; Jun Zhang
Journal:  Nat Commun       Date:  2020-07-21       Impact factor: 14.919

  7 in total

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