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γ-氨基丁酸(GABA)和5-羟色胺(5-HT)系统与小鼠中刺槐素的抗焦虑样作用有关。

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

作者信息

Liu Jie, Zhai Wei-Min, Yang Yuan-Xiao, Shi Jin-Li, Liu Qian-Tong, Liu Guo-Lin, Fang Nan, Li Jian, Guo Jian-You

机构信息

School of Chinese Materia Medica, Beijing University of Chinese Medicine, 6A Wangjing Central South Road, Chaoyang District, Beijing 100102, China.

Standard of Chinese medicine, State Pharmacopoeia Commission, 11A Law of Southern China, Chongwen District, Beijing 100061, China.

出版信息

Pharmacol Biochem Behav. 2015 Jan;128:41-9. doi: 10.1016/j.pbb.2014.11.003. Epub 2014 Nov 6.

Abstract

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 5mg/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 5mg/kg. In the open-field test, 5mg/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 γ-aminobutyric acid-A (GABAA) receptor antagonist flumazenil (3mg/kg, i.p.) and 5-hydroxytryptamine-1A (5-HT1A) receptor antagonist WAY-100635 (1mg/kg, i.p.). These results suggest that spinosin exerts anxiolytic-like effects, and its mechanism of action appears to be modulated by GABAA and 5-HT1A receptors.

摘要

本研究调查了酸枣仁(ZSS)中的主要黄酮类化合物之一斯皮诺素与已知抗焦虑药地西泮相比,在焦虑实验模型中的抗焦虑样作用。与对照组相比,重复给予斯皮诺素(2.5和5mg/kg/天,口服)显著增加了高架十字迷宫开放臂的进入次数百分比和停留时间。在明暗箱试验中,斯皮诺素在5mg/kg时发挥抗焦虑样作用。在旷场试验中,5mg/kg斯皮诺素增加了中央进入次数。斯皮诺素不影响自发活动。斯皮诺素在高架十字迷宫、明暗箱试验和旷场试验中的抗焦虑样作用被γ-氨基丁酸-A(GABAA)受体拮抗剂氟马西尼(3mg/kg,腹腔注射)和5-羟色胺-1A(5-HT1A)受体拮抗剂WAY-100635(1mg/kg,腹腔注射)阻断。这些结果表明,斯皮诺素发挥抗焦虑样作用,其作用机制似乎受GABAA和5-HT1A受体调节。

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