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乌拉尔甘草中甘草苷和异甘草苷在小鼠强迫游泳试验和悬尾试验中的抗抑郁样作用

Antidepressant-like effects of liquiritin and isoliquiritin from Glycyrrhiza uralensis in the forced swimming test and tail suspension test in mice.

作者信息

Wang Weixing, Hu Xinying, Zhao Zhiyu, Liu Peng, Hu Yuchi, Zhou Jianping, Zhou Dongfeng, Wang Zhibin, Guo Dean, Guo Hongzhu

机构信息

School of Pharmaceutical Sciences, Peking University, Beijing, China.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2008 Jul 1;32(5):1179-84. doi: 10.1016/j.pnpbp.2007.12.021. Epub 2008 Jan 18.

Abstract

Two classic animal behavior despair tests--the Forced Swimming Test (FST) and the Tail Suspension Test (TST) were used to evaluate the antidepressant activity of liquiritin and isoliquiritin from Glycyrrhiza uralensis in mice. It was observed that both liquiritin and isoliquiritin at doses of 10, 20 and 40 mg/kg significantly reduced the immobility time in the FST and TST in mice 30 min after treatment. Measurement of locomotor activity indicated that liquiritin and isoliquiritin had no central nervous system (CNS)-stimulating effects. The main monoamine neurotransmitters and their metabolites in mouse brain regions were also simultaneously determined by HPLC-ECD. It was found that these two compounds significantly increased the concentrations of the main neurotransmitters 5-HT and NE in the hippocampus, hypothalamus and cortex. Liquiritin and isoliquiritin also significantly reduced the ratio of 5-HIAA/5-HT in the hippocampus, hypothalamus and cortex, slowing down 5-HT metabolism compared with mice treated with vehicle+stress. In conclusion, liquiritin and isoliquiritin produced significant antidepressant-like effects, and their mechanism of action may be due to increased 5-HT and NE in the mouse hippocampus, hypothalamus and cortex.

摘要

采用两种经典的动物行为绝望试验——强迫游泳试验(FST)和悬尾试验(TST),来评估甘草中甘草苷和异甘草苷对小鼠的抗抑郁活性。观察发现,甘草苷和异甘草苷在10、20和40mg/kg剂量下,在处理后30分钟时能显著缩短小鼠在FST和TST中的不动时间。运动活性测量表明,甘草苷和异甘草苷没有中枢神经系统(CNS)刺激作用。还通过高效液相色谱-电化学检测法(HPLC-ECD)同时测定了小鼠脑区主要单胺类神经递质及其代谢产物。发现这两种化合物显著提高了海马体、下丘脑和皮层中主要神经递质5-羟色胺(5-HT)和去甲肾上腺素(NE)的浓度。甘草苷和异甘草苷还显著降低了海马体、下丘脑和皮层中5-羟吲哚乙酸(5-HIAA)/5-羟色胺(5-HT)的比值,与接受溶媒+应激处理的小鼠相比,减缓了5-羟色胺(5-HT)的代谢。总之,甘草苷和异甘草苷产生了显著的抗抑郁样作用,其作用机制可能是由于小鼠海马体、下丘脑和皮层中5-羟色胺(5-HT)和去甲肾上腺素(NE)增加所致。

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