Anxiolytic-like effects of ginsenosides on the elevated plus-maze model in mice

被引:40
作者
Cha, HY
Park, JH
Hong, JT
Yoo, HS
Song, S
Hwang, BY
Eun, JS
Oh, KW [1 ]
机构
[1] Chungbuk Natl Univ, Coll Pharm, Cheongju 361763, South Korea
[2] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[3] Woosuk Univ, Coll Pharm, Samrye 565701, South Korea
关键词
anxiolytic; elevated plus-maze; open arm; closed arm; ginsenoside; diazepam; locomotor activity;
D O I
10.1248/bpb.28.1621
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In a previous study, we reported that ginseng extract has anxiolytic-like effects in the elevated plus-maze model and that the ginseng saponin fraction plays an important role. This experiment was performed to investigate the anxiolytic-like effects of ginsenosides Rb-1, Rg(1), Rg(3)-R, and Rg(3)-S, and the Rg(5) and Rk mixture isolated from the ginseng saponin fraction in the elevated plus-maze. Furthermore, the anxiolytic-effects of Rb-1, Rg(1), Rg(3)-R, Rg(3)-S, and the Rg(5) and Rk mixture were compared with those of a well-known active anxiolytic drug (diazepam). The oral administration of ginsenoside Rb-1 significantly increased the number of open arm entries and the time spent on the open arm compared with those in the vehicle-treated group. Ginsenoside Rg(1) and the Rg(5) and Rk mixture also significantly increased the number of open arm entries and the time spent on the open arm. However, ginsenosides Rg(3)-R and Rg(3)-S did not increase the number of open arm entries or the time spent on the open arm. On the other hand, ginsenoside Rb-1 and the Rg(5) and Rk mixture decreased locomotor activity in a manner similar to diazepam. These data indicate that ginsenosides Rb-1, Rg(1), and the Rg(5) and Rk mixture have anxiolytic-like effects, but ginsenosides Rg(3)-R and Rg(3)-S do not in this model. We provide evidence that some ginsenosides may be useful for the treatment of anxiety.
引用
收藏
页码:1621 / 1625
页数:5
相关论文
共 31 条
[1]   A review of herbal medicines for psychiatric disorders [J].
Beaubrun, G ;
Gray, GE .
PSYCHIATRIC SERVICES, 2000, 51 (09) :1130-1134
[2]  
Cha Hwa-Young, 2004, Journal of Ginseng Research, V28, P132
[3]   Behavioral effects of diazepam in the murine plus-maze: Flumazenil antagonism of enhanced head dipping but not the disinhibition of open-arm avoidance [J].
Dalvi, A ;
Rodgers, RJ .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1999, 62 (04) :727-734
[4]   USE OF THE ELEVATED PLUS-MAZE IN THE SEARCH FOR NOVEL ANXIOLYTIC AGENTS [J].
DAWSON, GR ;
TRICKLEBANK, MD .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1995, 16 (02) :33-36
[5]   Trends in alternative medicine use in the United States, 1990-1997 - Results of a follow-up national survey [J].
Eisenberg, DM ;
Davis, RB ;
Ettner, SL ;
Appel, S ;
Wilkey, S ;
van Rompay, M ;
Kessler, RC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (18) :1569-1575
[6]   The effect of treatment regimen on the development of tolerance to the sedative and anxiolytic effects of diazepam [J].
Fernandes, C ;
Arnot, MI ;
Irvine, EE ;
Bateson, AN ;
Martin, IL ;
File, SE .
PSYCHOPHARMACOLOGY, 1999, 145 (03) :251-259
[7]  
Friede M, 2002, EUR PSYCHIAT, V17, p96S
[8]  
GRIFFITHS RR, 1987, ABUSE DEPENDENCE BEN, P1535
[9]   Ethnopharmacology in drug discovery: an analysis of its role and potential contribution [J].
Heinrich, M ;
Gibbons, S .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2001, 53 (04) :425-432
[10]   A review of the validity and variability of the elevated plus-maze as an animal model of anxiety [J].
Hogg, S .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1996, 54 (01) :21-30