Studies on the anxiolytic effects of Kai-Mai-Ta-Taso-Tang in Rodents

碩士 === 中國醫藥學院 === 中國醫藥研究所 === 86 === The present study was investigated the anxiolytic effects of Kan-Mai-Ta- Taso-Tang by the animal anxiety models: two-way active avoidance, black/white chamber, and elevated plus-maze. We also investigated the action mechanis...

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Bibliographic Details
Main Authors: Yang,Shu-Er, 楊淑娥
Other Authors: Hsieh, Ming-Tsuen
Format: Others
Language:zh-TW
Published: 1998
Online Access:http://ndltd.ncl.edu.tw/handle/57376519765835989016
Description
Summary:碩士 === 中國醫藥學院 === 中國醫藥研究所 === 86 === The present study was investigated the anxiolytic effects of Kan-Mai-Ta- Taso-Tang by the animal anxiety models: two-way active avoidance, black/white chamber, and elevated plus-maze. We also investigated the action mechanism of KM via combining with the drug altered the 5-HT neuron activities or using biochemical method. KM ( 0.3-2.0 g/kg, p.o. ) decreased the rats'' response counts of unconditioned stimulus and intertrial crossing in two-way active avoidance. In the elevated plus-maze, KM ( 0.3-1.0 g/kg, p.o. ) increased the percentage of the time spent in the open arms and entries, and decreased the percentage of the time spent in the closed arms and entries. However, KM ( 2.0 g/kg, p.o. ) prolonged the percentage of the time spent of mice in the closed arms. For mice in the black/white chamber, KM prolonged the time spent in the white chamber and decreased the time spent in the black chamber. KM ( 1.0, 2.0 g/kg, p.o. ) decreased the locomotor activities of mice. KM ( 0.3 g/kg, p.o. ) blocked the anxiogenic effect induced by 5-HTP, and enhanced the anxiolytic effects induced by PCPA, buspirone, p-MPPI and ritanserin in mice. The concentrations of monoamines and their metabolites in the brain stem of mice were detected by using High- performance liquid chromatography. KM decreased the 5-HT, NE, DA and 5-HIAA levels, and increased the VMA and HVA levels. From the above results, the mechamisms on the anxiolytic effects of KM may be related to the decrease in the 5-HT turnover rate via activating the activity of the presynaptic 5-HT1A autoreceptors and decreasing the activities of the postsynaptic 5-HT1A , 5-HT2 receptors