Kamishoyosan potentiates pentobarbital-induced sleep in socially isolated, ovariectomized mice.


Journal

Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310

Informations de publication

Date de publication:
05 Dec 2021
Historique:
received: 28 04 2021
revised: 28 06 2021
accepted: 27 08 2021
pubmed: 1 9 2021
medline: 27 1 2022
entrez: 31 8 2021
Statut: ppublish

Résumé

Sleep disorders are among the most common symptoms in both peri- and post-menopausal women. Kamishoyosan (KSS) is a Kampo medicine prescribed for the treatment of sleep disorders in menopausal women in Japan. However, its precise mechanism of action remains unclear. In the present study, we developed a new animal model of menopausal sleep disorders by inducing social isolation stress in ovariectomized mice. Using pentobarbital-induced sleeping time as an index, we aimed to investigate the effects of KSS and involvement of the benzodiazepine receptors. Eight-week-old, female ddY mice were ovariectomized or subjected to a sham operation (control) and housed in social isolation or groups for 9 weeks. The animals were divided into four groups, group-housed sham-operated, isolated sham-operated, group-housed ovariectomized, and socially isolated ovariectomized. Pentobarbital (50 mg/kg) was administered intraperitoneally (i.p.). Sleeping time was considered the period between the loss of righting reflex and its return (up to 180 min). KSS was administered orally (p.o.) 60 min before the test. Diazepam and flumazenil were administered i.p. 30 and 45 min before the test, respectively. On the day after administration, the mice were euthanized, and their uteri were weighed. Socially isolated, ovariectomized mice had shorter sleeping times than mice in all other groups. In mice with intact ovaries, diazepam (1 mg/kg, i.p.) considerably prolonged the pentobarbital-induced sleeping time, but KSS (30-1000 mg/kg, p.o.) did not. However, KSS (100 mg/kg, p.o.) significantly prolonged the pentobarbital-induced sleeping time in socially isolated ovariectomized mice. The prolongation of sleeping time mediated by KSS was reversed by flumazenil (3 mg/kg, i.p.). KSS potentiated pentobarbital-induced sleep in socially isolated, ovariectomized mice, and the benzodiazepine receptors are possibly involved in its pharmacological mechanism. These findings suggest that KSS is beneficial for the treatment of menopausal sleep disorders.

Identifiants

pubmed: 34464703
pii: S0378-8741(21)00814-X
doi: 10.1016/j.jep.2021.114585
pii:
doi:

Substances chimiques

Drugs, Chinese Herbal 0
Hypnotics and Sedatives 0
kamisyoyo san 0
Pentobarbital I4744080IR

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

114585

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Nobuaki Egashira (N)

Department of Pharmacy, Kyushu University Hospital, Fukuoka, 812-8582, Japan. Electronic address: egashira.nobuaki.696@m.kyushu-u.ac.jp.

Yu Goto (Y)

Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, 814-0180, Japan. Electronic address: k1876886@kadai.jp.

Hikari Iba (H)

Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, 814-0180, Japan. Electronic address: ihikari.0215@gmail.com.

Rikako Kawanaka (R)

Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, 814-0180, Japan. Electronic address: rikako0510@oita-u.ac.jp.

Ryota Takahashi (R)

Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, 814-0180, Japan. Electronic address: sakaida.kakiemon74632@gmail.com.

Chise Taniguchi (C)

Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, 814-0180, Japan. Electronic address: pd201006@cis.fukuoka-u.ac.jp.

Takuya Watanabe (T)

Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, 814-0180, Japan. Electronic address: twatanabe@fukuoka-u.ac.jp.

Kaori Kubota (K)

Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, 814-0180, Japan; A.I.G. Collaborative Research Institute for Aging and Brain Sciences, Fukuoka University, Fukuoka, 814-0180, Japan. Electronic address: kkubota@fukuoka-u.ac.jp.

Shutaro Katsurabayashi (S)

Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, 814-0180, Japan. Electronic address: shutarok@fukuoka-u.ac.jp.

Katsunori Iwasaki (K)

Department of Neuropharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, 814-0180, Japan; A.I.G. Collaborative Research Institute for Aging and Brain Sciences, Fukuoka University, Fukuoka, 814-0180, Japan. Electronic address: iwasakik@fukuoka-u.ac.jp.

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Classifications MeSH