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Lauflumide (NLS-4) Is a New Potent Wake-Promoting Compound

Psychostimulants are used for the treatment of excessive daytime sleepiness in a wide range of sleep disorders as well as in attention deficit hyperactivity disorder or cognitive impairment in neuropsychiatric disorders. Here, we tested in mice the wake-promoting properties of NLS-4 and its effects...

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Autores principales: Luca, Gianina, Bandarabadi, Mojtaba, Konofal, Eric, Lecendreux, Michel, Ferrié, Laurent, Figadère, Bruno, Tafti, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104159/
https://www.ncbi.nlm.nih.gov/pubmed/30158846
http://dx.doi.org/10.3389/fnins.2018.00519
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author Luca, Gianina
Bandarabadi, Mojtaba
Konofal, Eric
Lecendreux, Michel
Ferrié, Laurent
Figadère, Bruno
Tafti, Mehdi
author_facet Luca, Gianina
Bandarabadi, Mojtaba
Konofal, Eric
Lecendreux, Michel
Ferrié, Laurent
Figadère, Bruno
Tafti, Mehdi
author_sort Luca, Gianina
collection PubMed
description Psychostimulants are used for the treatment of excessive daytime sleepiness in a wide range of sleep disorders as well as in attention deficit hyperactivity disorder or cognitive impairment in neuropsychiatric disorders. Here, we tested in mice the wake-promoting properties of NLS-4 and its effects on the following sleep as compared with those of modafinil and vehicle. C57BL/6J mice were intraperitoneally injected with vehicle, NLS-4 (64 mg/kg), or modafinil (150 mg/kg) at light onset. EEG and EMG were recorded continuously for 24 h after injections and vigilance states as well as EEG power densities were analyzed. NLS-4 at 64 mg/kg induced significantly longer wakefulness duration than modafinil at 150 mg/kg. Although no significant sleep rebound was observed after sleep onset for both treatments as compared with their vehicles, modafinil-treated mice showed significantly more NREM sleep when compared to NLS-4. Spectral analysis of the NREM EEG after NLS-4 treatment indicated an increased power density in delta activity (0.75–3.5 Hz) and a decreased power in theta frequency range (6.25–7.25 Hz), while there was no differences after modafinil treatment. Also, time course analysis of the delta activity showed a significant increase only during the first 2 time intervals of sleep after NLS-4 treatment, while delta power was increased during the first 9 time intervals after modafinil. Our results indicate that NLS-4 is a highly potent wake-promoting drug with no sign of hypersomnia rebound. As opposed to modafinil, recovery sleep after NLS-4 treatment is characterized by less NREM amount and delta activity, suggesting a lower need for recovery despite longer drug-induced wakefulness.
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spelling pubmed-61041592018-08-29 Lauflumide (NLS-4) Is a New Potent Wake-Promoting Compound Luca, Gianina Bandarabadi, Mojtaba Konofal, Eric Lecendreux, Michel Ferrié, Laurent Figadère, Bruno Tafti, Mehdi Front Neurosci Neuroscience Psychostimulants are used for the treatment of excessive daytime sleepiness in a wide range of sleep disorders as well as in attention deficit hyperactivity disorder or cognitive impairment in neuropsychiatric disorders. Here, we tested in mice the wake-promoting properties of NLS-4 and its effects on the following sleep as compared with those of modafinil and vehicle. C57BL/6J mice were intraperitoneally injected with vehicle, NLS-4 (64 mg/kg), or modafinil (150 mg/kg) at light onset. EEG and EMG were recorded continuously for 24 h after injections and vigilance states as well as EEG power densities were analyzed. NLS-4 at 64 mg/kg induced significantly longer wakefulness duration than modafinil at 150 mg/kg. Although no significant sleep rebound was observed after sleep onset for both treatments as compared with their vehicles, modafinil-treated mice showed significantly more NREM sleep when compared to NLS-4. Spectral analysis of the NREM EEG after NLS-4 treatment indicated an increased power density in delta activity (0.75–3.5 Hz) and a decreased power in theta frequency range (6.25–7.25 Hz), while there was no differences after modafinil treatment. Also, time course analysis of the delta activity showed a significant increase only during the first 2 time intervals of sleep after NLS-4 treatment, while delta power was increased during the first 9 time intervals after modafinil. Our results indicate that NLS-4 is a highly potent wake-promoting drug with no sign of hypersomnia rebound. As opposed to modafinil, recovery sleep after NLS-4 treatment is characterized by less NREM amount and delta activity, suggesting a lower need for recovery despite longer drug-induced wakefulness. Frontiers Media S.A. 2018-08-15 /pmc/articles/PMC6104159/ /pubmed/30158846 http://dx.doi.org/10.3389/fnins.2018.00519 Text en Copyright © 2018 Luca, Bandarabadi, Konofal, Lecendreux, Ferrié, Figadère and Tafti. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Luca, Gianina
Bandarabadi, Mojtaba
Konofal, Eric
Lecendreux, Michel
Ferrié, Laurent
Figadère, Bruno
Tafti, Mehdi
Lauflumide (NLS-4) Is a New Potent Wake-Promoting Compound
title Lauflumide (NLS-4) Is a New Potent Wake-Promoting Compound
title_full Lauflumide (NLS-4) Is a New Potent Wake-Promoting Compound
title_fullStr Lauflumide (NLS-4) Is a New Potent Wake-Promoting Compound
title_full_unstemmed Lauflumide (NLS-4) Is a New Potent Wake-Promoting Compound
title_short Lauflumide (NLS-4) Is a New Potent Wake-Promoting Compound
title_sort lauflumide (nls-4) is a new potent wake-promoting compound
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104159/
https://www.ncbi.nlm.nih.gov/pubmed/30158846
http://dx.doi.org/10.3389/fnins.2018.00519
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