Wei Guining, Su Hua, He Fei, Lu Wenjie, Lu Guoshou, Huang Zhoufeng, Tan Xiao, Lin Xiao, Zeng Xianbiao, Wei Baowei, Chen Naihong, Chu Shifen, Su Qibiao, Chen Naihong, Lin Meiyu
Department of Pharmacology, Guangxi Institute of Chinese Medicine and Pharmaceutical Science, Nanning 530022, China.
State Key Laboratory of Bioactive Substances and Functions of Natural Medicines, Institute of Materia & Neuroscience Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
J Tradit Chin Med. 2018 Feb;38(1):12-21.
To investigate the antidepressant-like effect of active fraction of Polyrhachis vicina Roger (AFPR) in a rat depression model, and to elucidate the underlying mechanism.
AFPR was extracted with ethanol followed by petroleum ether. Its antidepressant-like effect was investigated in mice by tail suspension test (TST), forced swimming test (FST) and open field test (OPT). A repeated dose of reserpine (0.5 mg/kg, daily for 14 d) was used to establish a rat depression model. Fluoxetine was used as positive control agent. The effect of AFPR on reserpine-induced ptosis, hypothermia and akinesia, the levels of monoamines and their metabolites, and the activity of monoamine oxidase (MAO) in hippocampus and prefrontal cortex were determined.
Administration of AFPR by gavage at 160 and 320 mg/kg significantly reduced the duration of immobility in the FST and TST, and did not affect locomotor activity in the OPT. In the reserpine-induced depression model, AFPR attenuated anhedonia, demonstrated by reversing hypothermia, akinesia and sucrose consumption. AFPR significantly increased the concentration of monoamines, including dopamine, serotonin, noradrenaline and acetylcholine.
AFPR normalized the metabolism rates of noradrenaline, serotonin and dopamine, and the activity of MAO, which were altered by chronic reserpine exposure. The findings suggest that modulation of the monoaminergic neurotransmitter system likely underlies the antidepressant-like effect of AFPR.
研究拟黑多刺蚁活性部位(AFPR)在大鼠抑郁模型中的抗抑郁样作用,并阐明其潜在机制。
采用乙醇提取后用石油醚萃取的方法获得AFPR。通过悬尾试验(TST)、强迫游泳试验(FST)和旷场试验(OPT)研究其在小鼠体内的抗抑郁样作用。使用重复剂量的利血平(0.5mg/kg,每日1次,共14天)建立大鼠抑郁模型。氟西汀作为阳性对照药。测定AFPR对利血平诱导的眼睑下垂、体温过低和运动不能的影响,以及海马和前额叶皮质中单胺及其代谢产物的水平和单胺氧化酶(MAO)的活性。
以160和320mg/kg的剂量灌胃给予AFPR可显著缩短FST和TST中的不动时间,且不影响OPT中的运动活性。在利血平诱导的抑郁模型中,AFPR通过逆转体温过低、运动不能和蔗糖消耗减轻快感缺失。AFPR显著增加了包括多巴胺、5-羟色胺、去甲肾上腺素和乙酰胆碱在内的单胺浓度。
AFPR使慢性利血平暴露所改变的去甲肾上腺素、5-羟色胺和多巴胺的代谢率以及MAO的活性恢复正常。这些发现表明,单胺能神经递质系统的调节可能是AFPR抗抑郁样作用的基础。