Effects of aqueous extracts and volatile oils prepared from Huaxiang Anshen decoction on p-chlorophenylalanine-induced insomnia mice.


Journal

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

Informations de publication

Date de publication:
30 Jan 2024
Historique:
received: 23 07 2023
revised: 11 10 2023
accepted: 16 10 2023
medline: 27 11 2023
pubmed: 20 10 2023
entrez: 20 10 2023
Statut: ppublish

Résumé

Insomnia occurs frequently in modern society, and its common symptoms include difficulty in falling asleep and decreased sleep quality and time, memory, and attention. With the advantages of having few side-effects and reduced drug-dependence, a compound traditional Chinese medicine (TCM) prescription called Huaxiang Anshen Decoction (HAD) has been widely used in clinical practice in China mainly for primary insomnia treatment. Although the effects of volatile oils from TCM herbs have been increasingly reported, volatile oils in HAD are conventionally neglected because of its preparation process and clinical usage. Therefore, exploring the anti-insomnia effects of volatile oils from HAD is of great importance. The sedative and hypnotic effects of the conventional aqueous extracts, the volatile oils from HAD, and their combinations were investigated. The main components in HAD volatile oils (HAD-Oils), were analyzed through gas chromatography-mass spectrometry (GC-MS). The HAD volatile oil inclusion complex (HAD-OIC) was prepared with β-cyclodextrin, and characterized. P-chlorophenylalanine (PCPA) was used to induce insomnia mice model and the test groups of HAD aqueous extract (HAD-AE), HAD-OIC and their combination (AE-OIC). An open field test was used in evaluating the mice's activities, and the levels of 5-hydroxytryptamine (5-HT) in mice sera, glutamate (Glu) in the hypothalamus, and γ-aminobutyric acid (γ-GABA) and dopamine (DA) in the brain tissues were assayed by enzyme-linked immunosorbent assay (ELISA). A total 74 components in HAD-Oil were determined by GC/MS, and cyperenone (20.46%) and α-cyperone (10.39%) had the highest relative content. The characterization results of the physical phase showed that volatile oils were successfully encapsulated by β-cyclodextrin and HAD-OIC was produced. The average encapsulation rates of cyperenone and α-cyperone were 79.93% and 71.96%, respectively. The results of pharmacology study showed that all the test groups increased the body weight and decreased voluntary activity when compared with the model group (P < 0.05). The HAD-AE, HAD-OIC, and AE-OIC groups increased the levels of 5-HT in the sera and DA and Glu/γ-GABA in the brains, and AE-OIC groups showed better performance than the other test groups. HAD-Oil exerts sedative and hypnotic effects, which are increased when it is used with HAD-AEs. This result provides a favorable experimental evidence that volatile oils should be retained for the further development of HAD.

Identifiants

pubmed: 37858748
pii: S0378-8741(23)01201-1
doi: 10.1016/j.jep.2023.117331
pii:
doi:

Substances chimiques

Oils, Volatile 0
alpha-cyperone ZL24SG1C2D
Fenclonine R5J7E3L9SP
Serotonin 333DO1RDJY
Hypnotics and Sedatives 0
gamma-Aminobutyric Acid 56-12-2
Dopamine VTD58H1Z2X
beta-Cyclodextrins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

117331

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors report no conflicts of interest in this work.

Auteurs

Xinye Li (X)

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Chao He (C)

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Min Shen (M)

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Mingyun Wang (M)

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Jingwen Zhou (J)

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Dongying Chen (D)

Laboratory of Pharmaceutical Analysis, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.

Tong Zhang (T)

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Yiqiong Pu (Y)

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China. Electronic address: puyiqiong@shutcm.edu.cn.

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Classifications MeSH