The impact of sleep deprivation on sexual behaviors and FAAH expression in the prefrontal cortex of male rats.


Journal

Neuroscience letters
ISSN: 1872-7972
Titre abrégé: Neurosci Lett
Pays: Ireland
ID NLM: 7600130

Informations de publication

Date de publication:
14 09 2020
Historique:
received: 08 05 2020
revised: 27 06 2020
accepted: 14 07 2020
pubmed: 20 7 2020
medline: 24 4 2021
entrez: 20 7 2020
Statut: ppublish

Résumé

Sleep deprivation (SD) causes alterations in the function of the endocannabinoid (EC) system and also results in alteration in many behaviors such as increased anxiety, deteriorated alertness, memory deficits, as well as sexual behaviors. Controversial data about the effects of SD on sexual response are provided. Fatty acid amide hydrolase (FAAH), the enzymes involved in the degradation of the EC system play an important role in the function of the EC system. This study aimed to investigate the effect of REM SD (RSD) and total SD (TSD) on the sexual behaviors and FAAH expression in the prefrontal cortex (PFC) of male rats. RSD was carried out through the flower pot technique for 24 h and 48 h, and TSD also was induced by keeping awake the rats by gentle handling for 6 h. Immediately after RSD and TSD, sexual behaviors were recorded for 45 min. Sexual behaviors were reduced by both types of RSD and TSD. The deleterious effects of 24 h RSD were more severe compared with 6 h of TSD. Serum testosterone concentration was significantly higher after TSD but not RSD compared to the normal sleep (NS) group. FAAH expression in the PFC was significantly reduced after both RSD and TSD compared to the NS group. Given that the function of the EC system has been previously shown to change different behaviors such as sexual activity, our results could suggest that behavioral effects of both types of SD on sexual behavior may partially result from activation of this signaling pathway by the reduction of FAAH in the PFC.

Identifiants

pubmed: 32682844
pii: S0304-3940(20)30524-3
doi: 10.1016/j.neulet.2020.135254
pii:
doi:

Substances chimiques

Amidohydrolases EC 3.5.-
fatty-acid amide hydrolase EC 3.5.1.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

135254

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Mohammad Amini (M)

Neurophysiology Research Center, Urmia University of Medical Sciences, Urmia, Iran.

Ehsan Saboory (E)

Zanjan Metabolic Diseases Research Center, Zanjan University of Medical Sciences, Zanjan, Iran. Electronic address: saboory@zums.ac.ir.

Leila Derafshpour (L)

Neurophysiology Research Center, Urmia University of Medical Sciences, Urmia, Iran.

Ali Fakhari (A)

Research Center of Psychiatry and Behavioral Sciences, Aging Research Institute, Tabriz University of Medical Sciences, Tabriz, Iran.

Joseph C Wu (JC)

UC Irvine Department of Psychiatry and Human Behavior, Irvine, CA 92697, United States.

Richard Bruggeman (R)

University of Groningen, University Medical Center Groningen, Department of Psychiatry, Rob Giel Research Center, the Netherlands.

Fatemeh Asgharzadeh (F)

Neurophysiology Research Center, Urmia University of Medical Sciences, Urmia, Iran.

Ali Ahmadalipour (A)

Research Center of Psychiatry and Behavioral Sciences, Aging Research Institute, Tabriz University of Medical Sciences, Tabriz, Iran. Electronic address: alipoura@tbzmed.ac.ir.

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Classifications MeSH