Optimal Dose for Anti-depression Effect of Xiaoyaosan
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Optimal Dose for Anti-depression Effect of Xiaoyaosan
Chinese Journal of Experimental Traditional Medical FormulaeVol. 16, Issue 13, Pages: 194-198(2010)
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Published:2010
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CUI Jie, ZHENG Xing-yu, GAO Xiao-xia, et al. Optimal Dose for Anti-depression Effect of Xiaoyaosan[J]. Chinese journal of experimental traditional medical formulae, 2010, 16(13): 194-198.
DOI:
CUI Jie, ZHENG Xing-yu, GAO Xiao-xia, et al. Optimal Dose for Anti-depression Effect of Xiaoyaosan[J]. Chinese journal of experimental traditional medical formulae, 2010, 16(13): 194-198.DOI:
Optimal Dose for Anti-depression Effect of Xiaoyaosan
Objective: To screen the optimal dose of Xiaoyaosan in rats and to improve the anti-depression clinical effect. Method: In this research
two experiments were processed using the model of chronic unpredictable mild stress (CUMS). Amitriptyline and fluoxetine hydrochloride
venlafaxine hydrochloride were used as positive control
respectively. Behavioral changes
such as the weight
open-field
and sugar consumption
were measured. The urine was collected and analyzed by GC-MS
and the result was analyzed with SPSS and SIMCA-P. Result: The results of behavior changes and GC-MS suggested that the control group and model group were significantly different
which indicated that the model was successful. Comparing the treated group with the positive control group and the control group
the dose of 46.3 g ·kg-1 was closest to the control group
there was no significant difference. Conclusion: Xiaoyaosan has the obvious anti-depression effect
Metabolomic Analysis of Urine in Rat Model with Spleen-stomach Damp-heat Syndrome
Effect of Xiaoyaosan on Chronic Unpredictable Mild Stress Model in Rats
Analysis of Mechanism of Xiaoyaowan on Rats with Nonalcoholic Fatty Liver Disease and Syndrome of Liver Depression and Spleen Deficiency by H-NMR Metabolomics
Metabolomics of Roudoukou-8 San in Preprotecting Myocardial Ischemia Reperfusion Injury
Herbal Cake-separated Moxibustion Improves Cognitive Function in Rat Model of Chronic Fatigue Syndrome via PI3K/Beclin1 Signaling Pathway
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