GABA and 5-HT systems are implicated in the anxiolytic-like effect of spinosin in mice

被引:77
作者
Liu, Jie [1 ]
Zhai, Wei-Min [2 ]
Yang, Yuan-Xiao [3 ]
Shi, Jin-Li [1 ]
Liu, Qian-Tong [1 ]
Liu, Guo-Lin [1 ]
Fang, Nan [1 ]
Li, Jian [1 ]
Guo, Jian-You [4 ]
机构
[1] Beijing Univ Chinese Med, Sch Chinese Mat Med, Beijing 100102, Peoples R China
[2] State Pharmacopoeia Commiss, Standard Chinese Med, Beijing 100061, Peoples R China
[3] Zhejiang Chinese Med Univ, Sch Pharm, Hangzhou 310053, Zhejiang, Peoples R China
[4] Chinese Acad Sci, Inst Psychol, Key Lab Mental Hlth, Beijing 100101, Peoples R China
基金
美国国家科学基金会;
关键词
Spinosin; Elevated plus maze; Light/dark box; Open field test; GABA(A) receptor antagonist; 5-HT1A receptor antagonist; PENTOBARBITAL-INDUCED SLEEP; ELEVATED PLUS-MAZE; BENZODIAZEPINE-RECEPTOR; OPEN-FIELD; ANXIETY; INVOLVEMENT; BEHAVIOR; CLASSIFICATION; PHARMACOLOGY; FLAVONOIDS;
D O I
10.1016/j.pbb.2014.11.003
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The present study investigated the anxiolytic-like effects of spinosin, one of the major flavonoids in Ziziphi Spinosae Semen (ZSS), in experimental models of anxiety compared with a known anxiolytic, diazepam. Repeated treatment with spinosin (2.5 and 5 mg/kg/day, p.o.) significantly increased the percentage of entries into and time spent on the open arms of the elevated plus maze compared with the control group. In the light/dark box test, spinosin exerted an anxiolytic-like effect at 5 mg/kg. In the open-field test, 5 mg/kg spinosin increased the number of central entries. Spinosin did not affect spontaneous activity. The anxiolytic-like effects of spinosin in the elevated plus maze, light/dark box test, and open field test were blocked by the gamma-aminobutyric acid-A (GABA(A)) receptor antagonist flumazenil (3 mg/kg, i.p.) and 5-hydroxytryptamine-1A (5-HT1A) receptor antagonist WAY-100635 (1 mg/kg, i.p.). These results suggest that spinosin exerts anxiolytic-like effects, and its mechanism of action appears to be modulated by GABA(A) and 5-HT1A receptors. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:41 / 49
页数:9
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