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对叶野桐在急性小鼠模型中的抗抑郁作用

Antidepressant Effects of Mallotus oppositifolius in Acute Murine Models.

作者信息

Kukuia Kennedy K E, Mante Priscilla K, Woode Eric, Ameyaw Elvis O, Adongo Donatus W

机构信息

Department of Pharmacology, University of Ghana Medical School, College of Health Sciences, University of Ghana, Accra, Ghana.

Department of Pharmacology, Faculty of Pharmacy and Pharmaceutical Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

出版信息

ISRN Pharmacol. 2014 Mar 12;2014:324063. doi: 10.1155/2014/324063. eCollection 2014.

Abstract

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.

摘要

目的。对加纳用于中枢神经系统疾病的植物对叶野桐(Mallotus oppositifolius)叶的水醇提取物(MOE)进行强迫游泳试验(FST)和悬尾试验(TST),以研究其急性抗抑郁作用。结果。在FST和TST中,MOE(10、30和100 mg kg⁻¹)均显著缩短不动时间并降低不动频率。用色氨酸羟化酶抑制剂对氯苯丙氨酸(PCPA)腹腔注射200 mg kg⁻¹进行3天预处理,可逆转MOE在改良FST中引起的不动时间下降和游泳得分增加。单独用利血平(1 mg kg⁻¹)、单独用α-甲基多巴(400 mg kg⁻¹,腹腔注射)或两种药物联合预处理均未能逆转提取物在改良FST中引起的不动时间下降或游泳得分增加。该提取物增强了5-羟色胺诱导的头部抽搐反应频率。用甘氨酸/NMDA激动剂d-丝氨酸(600 mg kg⁻¹,腹腔注射)预处理可消除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,腹腔注射)在TST和改良FST中均增强了其效应。结论。该提取物在小鼠中表现出抗抑郁作用,其作用机制是通过增强5-羟色胺能神经传递和抑制甘氨酸/NMDA受体激活来介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c528/3972934/4d771d511a62/ISRN.PHARMACOLOGY2014-324063.001.jpg

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