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中药四逆散抗抑郁样作用及其在小鼠体内可能的作用机制研究

Screening of the antidepressant-like effect of the traditional Chinese medicinal formula Si-Ni-San and their possible mechanism of action in mice.

作者信息

Yi Li-Tao, Li Jing, Liu Bin-Bin, Li Cheng-Fu

机构信息

Department of Chemical and Pharmaceutical Engineering, College of Chemical Engineering, Huaqiao University, Xiamen, China.

出版信息

Pharmacognosy Res. 2013 Jan;5(1):36-42. doi: 10.4103/0974-8490.105647.

Abstract

BACKGROUND

The traditional Chinese medicine formula Si-Ni-San has well therapeutic applications in improvement of mental diseases including depression. However, the neuropharmacological and neuroendocrine mechanisms of the formula on antidepressant-like action have not been reported.

OBJECTIVE

Herein, we explored the antidepressant-like effect and its mechanism of Si-Ni-San.

MATERIALS AND METHODS

Acute effect of Si-Ni-San on the immobility time was assessed in the mouse forced swim test (FST) and tail suspension test (TST). Moreover, we investigated the neurochemical, neuroendocrine, and neurotrophin systems involved in the antidepressant-like effect of this formula.

RESULTS

Si-Ni-San significantly decreased the immobility time after acute treatment in the mouse TST (1300 mg/kg) but not in the FST compared with the control group. In addition, pretreatment of mice with PCPA or AMPT prevented the anti-immobility effect of Si-Ni-San (1300 mg/kg) in the TST. Moreover, acute Si-Ni-San (1300 mg/kg) decreased serum corticosterone levels, elevated serotonin (5-HT), norepinephrine (NE), and dopamine (DA) levels without affecting brain-derived neurotrophic factor (BDNF) levels in the whole brain exposed to TST.

CONCLUSION

The acute antidepressant-like action of Si-Ni-San is mediated by the monoaminergic and neuroendocrine systems although underlying mechanism still remains to be further elucidated, and this formula should be further investigated as an alternative therapeutic approach for the treatment of depression.

摘要

背景

中药方剂四逆散在改善包括抑郁症在内的精神疾病方面具有良好的治疗应用。然而,该方剂抗抑郁样作用的神经药理学和神经内分泌机制尚未见报道。

目的

在此,我们探讨了四逆散的抗抑郁样作用及其机制。

材料与方法

在小鼠强迫游泳试验(FST)和悬尾试验(TST)中评估四逆散对不动时间的急性作用。此外,我们研究了参与该方剂抗抑郁样作用的神经化学、神经内分泌和神经营养因子系统。

结果

与对照组相比,四逆散在小鼠TST中急性给药(1300mg/kg)后显著缩短了不动时间,但在FST中未观察到该作用。此外,用对氯苯丙氨酸(PCPA)或α-甲基对酪氨酸(AMPT)预处理小鼠可阻断四逆散(1300mg/kg)在TST中的抗不动作用。此外,急性给予四逆散(1300mg/kg)可降低血清皮质酮水平,升高血清素(5-HT)、去甲肾上腺素(NE)和多巴胺(DA)水平,而不影响TST处理后全脑中脑源性神经营养因子(BDNF)水平。

结论

四逆散的急性抗抑郁样作用由单胺能和神经内分泌系统介导,尽管其潜在机制仍有待进一步阐明,该方剂作为抑郁症的替代治疗方法应进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5352/3579018/13923b4f21fe/PR-5-36-g001.jpg

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