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甘草中甘草苷在慢性可变应激诱导的抑郁模型大鼠中的抗抑郁样作用

Antidepressant-like effect of liquiritin from Glycyrrhiza uralensis in chronic variable stress induced depression model rats.

作者信息

Zhao Zhiyu, Wang Weixing, Guo Hongzhu, Zhou Dongfeng

机构信息

Key Laboratory for Mental Health, Ministry of Health, Institute of Mental Health, Peking University, 51 Huayuan Bei Road, Haidian District, Beijing 100083, PR China.

出版信息

Behav Brain Res. 2008 Dec 1;194(1):108-13. doi: 10.1016/j.bbr.2008.06.030. Epub 2008 Jul 4.

Abstract

Many flavonoids extracted from nature plants have been reported to exert antidepressant-like effect in animal studies. The present study was designed to observe the effects of liquiritin, a flavone compound derived from Glycyrrhiza uralensis, on the behaviors of chronic variable stress induced depression model rats and to explore the possible association between its antidepressant-like effect and antioxidative activity by measuring erythrocyte superoxide dismutase (SOD) activity and plasma malondialdehyde (MDA) level of the experimental animals. With the exposure to stressor once daily for consecutive 5 weeks, liquiritin and a positive control drug fluoxetine were administered via gastric intubation to rats once daily for consecutive 3 weeks from the 3rd week. The results showed that CVS reduced open-field activity and sucrose consumption significantly, but increased immobility time in forced swimming test. Treatment of liquiritin could effectively reverse alteration in immobility time and sucrose consumption but did not show significant effect on open-field activity. Moreover, liquiritin could increase SOD activity, inhibit lipid peroxidation, and lessen production of MDA, while fluoxetine did not. In conclusion, the present study demonstrated a potential antidepressant-like effect of liquiritin treatment on chronic variable stress induced depression model rats, which might be related to defense of liquiritin against oxidative stress.

摘要

据报道,从天然植物中提取的许多黄酮类化合物在动物研究中具有抗抑郁样作用。本研究旨在观察从甘草中提取的黄酮类化合物甘草苷对慢性可变应激诱导的抑郁模型大鼠行为的影响,并通过测量实验动物的红细胞超氧化物歧化酶(SOD)活性和血浆丙二醛(MDA)水平,探讨其抗抑郁样作用与抗氧化活性之间的可能关联。连续5周每天对大鼠施加一次应激源,从第3周开始连续3周每天通过胃管给大鼠灌胃甘草苷和阳性对照药物氟西汀。结果表明,慢性可变应激显著降低了旷场活动和蔗糖消耗,但增加了强迫游泳试验中的不动时间。甘草苷治疗可有效逆转不动时间和蔗糖消耗的改变,但对旷场活动无显著影响。此外,甘草苷可增加SOD活性,抑制脂质过氧化,并减少MDA的产生,而氟西汀则没有。总之,本研究证明了甘草苷治疗对慢性可变应激诱导的抑郁模型大鼠具有潜在的抗抑郁样作用,这可能与甘草苷对氧化应激的防御作用有关。

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