荷花对急性小鼠模型的抗抑郁作用。

ISRN Pharmacology Pub Date : 2014-03-12 eCollection Date: 2014-01-01 DOI:10.1155/2014/324063
Kennedy K E Kukuia, Priscilla K Mante, Eric Woode, Elvis O Ameyaw, Donatus W Adongo
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引用次数: 15

摘要

目标。在强迫游泳(FST)和悬尾试验(TST)中,研究了加纳用于中枢神经系统条件的植物Mallotus oppositifolius (MOE)叶子的水酒精提取物的急性抗抑郁作用。结果。在FST和TST中,MOE(10、30和100 mg kg(-1))显著减少了静止时间和频率。用200 mg kg(-1), i.p,对氯苯丙氨酸(PCPA),一种色氨酸羟化酶抑制剂,预处理3天,逆转了MOE诱导的静止能力下降和游泳分数增加。单独用利血平(1 mg kg(-1))、单独用α -甲基多巴(400 mg kg(-1), i.p)或两种药物联合预处理,都不能逆转由改性FST中提取物引起的不动能力下降或游泳评分增加。该提取物可增强5-羟色胺诱导的头抽搐反应频率。用甘氨酸/NMDA激动剂d-丝氨酸(600 mg kg(-1), i.p)预处理可以消除MOE的行为效应,而甘氨酸/NMDA部分激动剂d-环丝氨酸(2.5 mg kg(-1), i.p)在TST和改性FST中都增强了MOE的作用。结论。其抗抑郁作用是通过增强血清素神经传递和抑制甘氨酸/NMDA受体的激活来实现的。
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Antidepressant Effects of Mallotus oppositifolius in Acute Murine Models.

Objective. Hydroalcoholic extract of leaves of Mallotus oppositifolius (MOE), a plant used for CNS conditions in Ghana, was investigated for acute antidepressant effects in the forced swimming (FST) and tail suspension tests (TST). Results. In both FST and TST, MOE (10, 30, and 100 mg kg(-1)) significantly decreased immobility periods and frequencies. A 3-day pretreatment with 200 mg kg(-1), i.p., para-chlorophenylalanine (PCPA), a tryptophan hydroxylase inhibitor, reversed the decline in immobility and the increase of swimming score induced by MOE in the modified FST. Pretreatment with reserpine alone (1 mg kg(-1)), α -methyldopa alone (400 mg kg(-1), i.p.), or a combination of both drugs failed to reverse the decline in immobility or the increase in swimming score caused by the extract in the modified FST. The extract potentiated the frequency of head twitch responses induced by 5-hydroxytryptamine. Pretreatment with d-serine (600 mg kg(-1), i.p.), glycine/NMDA agonist, abolished the behavioural effects of MOE while d-cycloserine (2.5 mg kg(-1), i.p.), a glycine/NMDA partial agonist, potentiated it in both TST and modified FST. Conclusion. The extract exhibited antidepressant effects in mice which is mediated by enhancement of serotoninergic neurotransmission and inhibition of glycine/NMDA receptor activation.

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