Sleep and neurochemical modulation by cannabidiolic acid methyl ester in rats.
Adenosine
Cannabinoids
Dopamine
Sleep
Wakefulness
Journal
Brain research bulletin
ISSN: 1873-2747
Titre abrégé: Brain Res Bull
Pays: United States
ID NLM: 7605818
Informations de publication
Date de publication:
02 2020
02 2020
Historique:
received:
12
08
2019
revised:
25
11
2019
accepted:
10
12
2019
pubmed:
16
12
2019
medline:
4
6
2021
entrez:
16
12
2019
Statut:
ppublish
Résumé
Cannabidiolic acid methyl ester (HU-580) is a more stable compound than cannabidiolic acid (CBDA) which has been shown to be effective in reducing nausea, anxiety, depression behaviors in animal models. Here we extend the investigation of this compound to determine its effect on the sleep-wake cycle in male Wistar rats. HU-580 dose-dependently (0.1, 1.0 or 100 μg/Kg, i.p.) prolonged wakefulness (W) and decreased slow wave sleep (SWS) duration whereas rapid eye movement sleep (REMS) showed no statistical change. In addition, the brain microdialysis probes either placed at nucleus accumbens (NAc) or into the basal forebrain in freely moving animals were used to evaluate the effects of HU-580 treatment on neurotransmitters related to the sleep-wake cycle modulation. HU-580 enhanced extracellular levels of dopamine, serotonin collected from NAc while adenosine and acetylcholine were increased in basal forebrain. In summary, HU-580 seems to possess wake-promoting pharmacological properties and enhances the levels of wake-related neurochemicals. This is the first report of effects of HU-580 on sleep modulation expanding the very limited existent data on the neurobiological effects of HU-580 on rats.
Identifiants
pubmed: 31838151
pii: S0361-9230(19)30630-6
doi: 10.1016/j.brainresbull.2019.12.006
pii:
doi:
Substances chimiques
Biogenic Monoamines
0
Cannabinoids
0
HU-580
0
Wakefulness-Promoting Agents
0
Adenosine
K72T3FS567
Acetylcholine
N9YNS0M02X
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
166-173Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.