结论：四逆散有明显的催眠作用。
Conclusions: Sinisan has a significant pharmacological role of hypnotic.
经方四逆散具有一定的保肝作用。
Classic prescription Sinisan has certain protective effect on liver injury.
结论：四逆散具有抑制小鼠小肠推进的作用。
Conclusion: Sinisan could restrain the small intestine propulsion function of mice.
同时也发现四逆散还能扩张小白鼠耳廓血管。
目的：观察四逆散对小鼠小肠推进功能的影响。
Objective: To observe the effect of Sinisan on small intestine propulsion function of mice.
目的比较四逆汤煎剂和缓释片两种剂型的毒性。
Objective to compare the toxicity of Sini decoction with the toxicity of Sini Sustained Release Tablets.
观察经方四逆散对肝损害的保护作用及机制研究。
Objective To observe the protective effect of classic prescription Sinisan and the mechanism on liver injury.
结论大孔树脂吸附法可用于加味四逆颗粒的精制。
Conclusion Macroporous resin adsorption method can be used for refining Jiawei Sini Granules.
目的观察加味四逆散治疗恶劣心境障碍的临床疗效。
Objective To observe the clinical effects of Jiawei Sini Decoction in the treatment of Dysthymia.
观察四逆汤加味对心绞痛型冠心病心肌收缩力的影响。
To observe the influence of Sini Decoction on cardiac contractility in coronary heart disease with angina pectoris.
同时，四逆汤还能降低缺血心肌丙二醛和乳酸的浓度。
Results indicate that SD can increase ATP content and reduce consumption of glycogen in IM, and decrease concentrations of MDA and lactic acid of IM.
经方四逆散能使肝损害小鼠肝组织病理变化程度明显减轻。
The extent of pathological injury of liver tissue was alleviated markedly.
目的：研究微量元素与四逆汤组方原则及功能主治的关系。
Objective: To study the relationship of trace elements and the principle of formulating Sini Tang, as well as the functions of curing for Sini Tang.
方法：大鼠随机分为3组：正常对照组、模型组、加味四逆散组。
METHODS: Wistar rats were randomly divided into 3 groups: control, model and JWSNS group.
方法：昆明种小鼠，随机分为对照组、缺血组、缺血加四逆汤组。
METHODS: Kunming mice were randomly divided into control group, ischemic group and Sini decoction group.
结果：缺血加四逆汤组gst基因表达显著强于对照组及缺血组。
RESULTS: the expression of GST mRNA in Sini decoction group was significantly up-regulated compared with the ischemic group and control group.
目的观察四逆汤对失血性休克大鼠心功能的保护作用及其机制探讨。
OBJECTIVE To study the protective effect of Sini Tang on cardiac function of hemorrhagic shock rats.
结论：复方玄驹胶囊联合加味四逆散疗效确切，未见明显不良反应。
Conclusion: Compound Xuanju capsule combined MSP effective, no significant adverse reactions.
目的研究附子中脂类生物碱（脂碱）的溶解性，确定四逆汤中脂碱的来源。
Objective To study the solubility of lipo-alkaloids from prepared aconite root(Radix Aconiti Lateralis Preparata) and identify the sources of lipo-alkaloids in Sini Decoction.
结论：可以采用阳离子树脂纯化四逆散总生物碱，该纯化工艺简单、经济。
Conclusion: Total alkaloids from Sinisan can be purified by cation resins. The purification process is simple and affordable.
目的观察加味四逆散对大鼠恶劣心境障碍模型纹状体单胺类神经递质的影响。
Objective To investigate the effect of Jiawei Sini powder on monoamine neurotransmitters in striatum of rat dysthymic disorder Model.
目的：观察加味四逆散对大鼠恶劣心境障碍模型海马单胺类神经递质的影响。
Objective: To investigate the effect of Jiawei Sini Powder on monoamine transmitters in Hippocampus of Rat Dysthymic disorder model.
目的：观察加味四逆散对大鼠恶劣心境障碍模型额叶单胺类神经递质的影响。
Objective: To investigate the effect of Jiawei Sini Powder on monoamine transmitters in frontal lobe of Rat Dysthymic disorder Model.
目的：探讨四逆汤对缺血心肌谷胱甘肽s转移酶(GST)基因表达的影响。
AIM: To detect the effect of Sini decoction on glutathione S-transferase (GST) mRNA expression in the ischemic myocardium.
四逆汤加味对改善心功能，调节血脂代谢有明显治疗作用，有助于提高远期疗效。
Sini Decoction has obvious therapeutic effect on improvement of cardiac function, regulation of blood lipid metabolism, and can help to increase the long-term effect.
目的对加味四逆颗粒大孔树脂吸附精制的方法进行工艺考察，选取最佳工艺条件。
Objective To optimize the conditions of Jiawei Sini granules by inspecting the macroporous resin adsorption refined methods.
目的：观察四逆汤(SND)对大鼠肠缺血再灌注后小肠上皮细胞超微结构的影响。
AIM: To investigate the effect of Sini decoction (SND) on the ultrastructure of small intestinal epithelial cells in rats with intestinal ischemia-reperfusion.
目的比较四逆汤超微颗粒和传统饮片两种不同荆型对豚鼠离体心脏作用是否存在差别。
Objective To observe the difference between traditional cut crude drug(TC- CD)and ultra-micro granule drug (UGD) in Sini decoction (SD) on the guinea pigs' heart in vitro.
目的比较四逆汤超微颗粒和传统饮片两种不同荆型对豚鼠离体心脏作用是否存在差别。
Objective To observe the difference between traditional cut crude drug(TC- CD)and ultra-micro granule drug (UGD) in Sini decoction (SD) on the guinea pigs' heart in vitro.
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