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

被引:246
作者
Zhao, Zhiyu [2 ]
Wang, Weixing [1 ]
Guo, Hongzhu [1 ]
Zhou, Dongfeng [2 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, Div Pharmacognost Biotechnol, Beijing 100083, Peoples R China
[2] Peking Univ, Inst Mental Hlth, Minist Hlth, Key Lab Mental Hlth, Beijing 100083, Peoples R China
基金
北京市自然科学基金;
关键词
liquiritin; Glycyrrhiza uralensis; antidepressant-like; chronic variable stress; forced swim test; superoxide dismutase; malondialdehyde;
D O I
10.1016/j.bbr.2008.06.030
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 [法学]; 0303 [社会学]; 030303 [人类学]; 04 [教育学]; 0402 [心理学];
摘要
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 Fats, which might be related to defense of liquiritin against oxidative stress. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:108 / 113
页数:6
相关论文
共 50 条
[1]
Antidepressant effect of an ethanolic extract of the leaves of Cissampelos sympodialis in rats and mice [J].
Almeida, RN ;
Navarro, DS ;
de Assis, TS ;
de Medeiros, IA ;
Thomas, G .
JOURNAL OF ETHNOPHARMACOLOGY, 1998, 63 (03) :247-252
[2]
DEPRESSION AS A CONSEQUENCE OF INADEQUATE NEUROCHEMICAL ADAPTATION IN RESPONSE TO STRESSORS [J].
ANISMAN, H ;
ZACHARKO, RM .
BRITISH JOURNAL OF PSYCHIATRY, 1992, 160 :36-43
[3]
Antioxidant activity of DHC-1, an herbal formulation, in experimentally-induced cardiac and renal damage [J].
Bafna, PA ;
Balaraman, R .
PHYTOTHERAPY RESEARCH, 2005, 19 (03) :216-221
[4]
Antioxidative enzyme activities and lipid peroxidation in major depression:: alterations by antidepressant treatments [J].
Bilici, M ;
Efe, H ;
Köroglu, MA ;
Uydu, HA ;
Bekaroglu, M ;
Deger, O .
JOURNAL OF AFFECTIVE DISORDERS, 2001, 64 (01) :43-51
[5]
Flavonoids from Hypericum perforatum show antidepressant activity in the forced swimming test [J].
Butterweck, V ;
Jürgenliemk, G ;
Nahrstedt, A ;
Winterhoff, H .
PLANTA MEDICA, 2000, 66 (01) :3-6
[6]
Antidepressant effects of Apocynum venetum leaves in a forced swimming test [J].
Butterweck, V ;
Nishibe, S ;
Sasaki, T ;
Uchida, M .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2001, 24 (07) :848-851
[7]
Antidepressant-like components of Hypericum perforatum extracts:: An overview of their pharmacokinetics and metabolism [J].
Caccia, S .
CURRENT DRUG METABOLISM, 2005, 6 (06) :531-543
[8]
Charney Dennis S, 2004, Sci STKE, V2004, pre5, DOI 10.1126/stke.2252004re5
[9]
FLAVONOIDS AS SUPEROXIDE SCAVENGERS AND ANTIOXIDANTS [J].
CHEN, YT ;
ZHENG, RL ;
JIA, ZJ ;
JU, Y .
FREE RADICAL BIOLOGY AND MEDICINE, 1990, 9 (01) :19-21
[10]
Antidepressant-like activity of Glycyrrhiza glabra L. in mouse models of immobility tests [J].
Dhingra, D ;
Sharma, A .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2006, 30 (03) :449-454