Narcolepsy and Orexins: An Example of Progress in Sleep Research

Narcolepsy is a chronic neurodegenerative disease caused by a deficiency of orexin-producing neurons in the lateral hypothalamus (LH). It is clinically characterized by excessive daytime sleepiness and by intrusions into wakefulness of physiological aspects of rapid eye movement (REM) sleep such as...

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Main Authors: Alberto K De La Herrán-Arita, Magdalena eGuerra-Crespo, René eDrucker-Colin
Format: Article
Language:English
Published: Frontiers Media S.A. 2011-04-01
Series:Frontiers in Neurology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fneur.2011.00026/full
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spelling doaj-774217a5e10e476aac6c6415673ab4312020-11-24T22:57:03ZengFrontiers Media S.A.Frontiers in Neurology1664-22952011-04-01210.3389/fneur.2011.0002610208Narcolepsy and Orexins: An Example of Progress in Sleep ResearchAlberto K De La Herrán-Arita0Magdalena eGuerra-Crespo1René eDrucker-Colin2Universidad Nacional Autónoma de MéxicoUniversidad Nacional Autónoma de MéxicoUniversidad Nacional Autónoma de MéxicoNarcolepsy is a chronic neurodegenerative disease caused by a deficiency of orexin-producing neurons in the lateral hypothalamus (LH). It is clinically characterized by excessive daytime sleepiness and by intrusions into wakefulness of physiological aspects of rapid eye movement (REM) sleep such as cataplexy, sleep paralysis and hypnagogic hallucinations. The major pathophysiology of narcolepsy has been recently described on the bases of the discovery of the neuropeptides named orexins (hypocretins) in 1998; considerable evidence, summarized below, demonstrates that narcolepsy is the result of alterations in the genes involved in the pathology of the orexin ligand or its receptor. Deficient orexin transmission is sufficient to produce narcolepsy, as we describe here, animal models with dysregulated orexin signaling exhibit a narcolepsy-like phenotype. Remarkably, these narcoleptic models have different alterations of the orexinergic circuit, this diversity provide us with the means for making comparison, and have a better understanding of orexin cell physiology.It is of particular interest that the most remarkable findings regarding this sleep disorder were fortuitous and due to keen observations. Sleep is a highly intricate and regulated state, and narcolepsy is a disorder that still remains as one of the unsolved mysteries in science. Nevertheless, advances and development of technology in neuroscience will provide us with the necessary tools to unravel the narcolepsy puzzle in the near future.Through an evaluation of the scientific literature we traced an updated picture of narcolepsy and orexins in order to provide insight into the means by which neurobiological knowledge is constructed.http://journal.frontiersin.org/Journal/10.3389/fneur.2011.00026/fullHypothalamusNarcolepsySleepOrexins
collection DOAJ
language English
format Article
sources DOAJ
author Alberto K De La Herrán-Arita
Magdalena eGuerra-Crespo
René eDrucker-Colin
spellingShingle Alberto K De La Herrán-Arita
Magdalena eGuerra-Crespo
René eDrucker-Colin
Narcolepsy and Orexins: An Example of Progress in Sleep Research
Frontiers in Neurology
Hypothalamus
Narcolepsy
Sleep
Orexins
author_facet Alberto K De La Herrán-Arita
Magdalena eGuerra-Crespo
René eDrucker-Colin
author_sort Alberto K De La Herrán-Arita
title Narcolepsy and Orexins: An Example of Progress in Sleep Research
title_short Narcolepsy and Orexins: An Example of Progress in Sleep Research
title_full Narcolepsy and Orexins: An Example of Progress in Sleep Research
title_fullStr Narcolepsy and Orexins: An Example of Progress in Sleep Research
title_full_unstemmed Narcolepsy and Orexins: An Example of Progress in Sleep Research
title_sort narcolepsy and orexins: an example of progress in sleep research
publisher Frontiers Media S.A.
series Frontiers in Neurology
issn 1664-2295
publishDate 2011-04-01
description Narcolepsy is a chronic neurodegenerative disease caused by a deficiency of orexin-producing neurons in the lateral hypothalamus (LH). It is clinically characterized by excessive daytime sleepiness and by intrusions into wakefulness of physiological aspects of rapid eye movement (REM) sleep such as cataplexy, sleep paralysis and hypnagogic hallucinations. The major pathophysiology of narcolepsy has been recently described on the bases of the discovery of the neuropeptides named orexins (hypocretins) in 1998; considerable evidence, summarized below, demonstrates that narcolepsy is the result of alterations in the genes involved in the pathology of the orexin ligand or its receptor. Deficient orexin transmission is sufficient to produce narcolepsy, as we describe here, animal models with dysregulated orexin signaling exhibit a narcolepsy-like phenotype. Remarkably, these narcoleptic models have different alterations of the orexinergic circuit, this diversity provide us with the means for making comparison, and have a better understanding of orexin cell physiology.It is of particular interest that the most remarkable findings regarding this sleep disorder were fortuitous and due to keen observations. Sleep is a highly intricate and regulated state, and narcolepsy is a disorder that still remains as one of the unsolved mysteries in science. Nevertheless, advances and development of technology in neuroscience will provide us with the necessary tools to unravel the narcolepsy puzzle in the near future.Through an evaluation of the scientific literature we traced an updated picture of narcolepsy and orexins in order to provide insight into the means by which neurobiological knowledge is constructed.
topic Hypothalamus
Narcolepsy
Sleep
Orexins
url http://journal.frontiersin.org/Journal/10.3389/fneur.2011.00026/full
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