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Journal of Ethnopharmacology
Volume 111, Issue 3, 22 May 2007, Pages 613-618
 
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doi:10.1016/j.jep.2007.01.009    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2007 Elsevier Ireland Ltd All rights reserved.

Anxiolytic effect of saponins from Panax quinquefolium in mice

Xiu-Yan Weia, Jing-Yu Yanga, Jin-Hui Wangb and Chun-Fu Wua, Corresponding Author Contact Information, E-mail The Corresponding Author, E-mail The Corresponding Author

aDepartment of Pharmacology, Shenyang Pharmaceutical University, Shenyang 110016, PR China bDepartment of Chemistry for Natural Drugs, Shenyang Pharmaceutical University, Shenyang 110016, PR China

Received 21 September 2006; 
revised 3 January 2007; 
accepted 9 January 2007. 
Available online 14 January 2007.

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Abstract

The anxiolytic effect of the saponins from Aniliaeea Panax quinquefolium L. (PQS) was studied in male mice by using a number of experimental paradigms of anxiety and compared with that of the known anxiolytic compound diazepam. Use of the elevated plus-maze test revealed that PQS (50 mg/kg, p.o.) and diazepam (2.5 mg/kg, p.o.) increased the percentage of time and entries spent in open arms. In the light/dark test, PQS (50 and 100 mg/kg, p.o.) and diazepam (2.5 mg/kg, p.o.) prolonged the time spent in the light area. In the hole-board test, PQS (50 and 100 mg/kg, p.o.) and diazepam (2.5 mg/kg, p.o.) significantly increased both head-dip counts and head-dip duration. Both PQS (50 and 100 mg/kg, p.o.) and diazepam (2.5 mg/kg, p.o.) decreased the total fighting time in the isolation-induced aggressive test. Since PQS, in contrast to diazepam, had no effect on locomotion in these tests, its side-effect profile might be considered superior to the benzodiazepines. Thus, the present findings suggest that PQS might be a potential candidate for use as an anxiolytic drug.

Keywords: Anxiolytic; PQS; Elevated plus-maze test; Hole-board test; Light-dark test; Isolation-induced aggressive test

Article Outline

1. Introduction
2. Materials and methods
2.1. Plant material
2.2. Preparation of extracts
2.3. Animals
2.4. Drugs
2.5. Procedures
2.5.1. Elevated plus-maze test
2.5.2. Light/dark test
2.5.3. The hole-board test
2.5.4. Isolation-induced aggressive test
2.6. Statistical analysis
3. Results
3.1. Elevated plus-maze test
3.2. Light/dark test
3.3. The hole-board test
3.4. Isolation-induced aggressive test
4. Discussion and conclusions
References




 
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