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Antidepressant-like effect of extract from Polygala paniculata: Involvement of the monoaminergic systems

机译:远志提取物的抗抑郁样作用:单胺能系统的参与

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Context: Polygala paniculata Linnaeus (Polygalaceae) has shown neuroprotective effects, but there is no report about its antidepressant potential. Objective: The antidepressant-like effect of the hydroalcoholic extract from P. paniculata and some of the possible mechanisms involved in this effect were investigated in forced swimming test (FST). Materials and methods: Mice received extract by oral route and were submitted to FST and open-field test. Animals were forced to swim and the total immobility time was registered (6-min period). A reduction in the immobility time is considered an antidepressant-like effect. In order to investigate the involvement of the monoaminergic systems, mice were treated with pharmacological antagonists before administration of the extract. Results: The acute administration of the hydroalcoholic extract from P. paniculata produced an antidepressant-like effect, since it significantly reduced the immobility time in FST (0.01–30?mg/kg) as compared to control group, without changing locomotor activity. Pretreatment of mice with yohimbine (1?mg/kg, i.p., α2-adrenoceptor antagonist), propranolol (1?mg/kg, i.p., β-adrenoceptor antagonist), SCH23390 (0.05?mg/kg, s.c., dopamine D1 receptor antagonist) or sulpiride (50?mg/kg, i.p., dopamine D2 receptor antagonist) prevented the antidepressant-like effect of the extract in FST (30?mg/kg). Moreover, ketanserin (5?mg/kg, i.p., preferential 5-HT2A receptor antagonist) enhanced the effect of the extract in FST. Discussion and conclusion: The results of the present study indicate that the extract from P. paniculata has an antidepressant-like action that is likely mediated by an interaction with the serotonergic (5-HT2A receptors), noradrenergic (α2 and β-receptor) and dopaminergic (D1 and D2 receptors) systems.
机译:背景:远志(Polygala paniculata Linnaeus)(Polygalaceae)已显示出神经保护作用,但尚无抗抑郁潜力的报道。目的:在强迫游泳试验(FST)中研究了P. paniculata的水醇提取物的抗抑郁样作用及其可能的机制。材料和方法:小鼠通过口服途径接受提取物,并接受FST和野外试验。强迫动物游泳并记录总的不动时间(6分钟)。固定时间的减少被认为是抗抑郁药样的作用。为了研究单胺能系统的参与,在给予提取物之前用药理拮抗剂治疗小鼠。结果:急性给药的P. paniculata的水醇提取物产生了抗抑郁样作用,因为与对照组相比,它显着减少了FST的固定时间(0.01–30?mg / kg),而没有改变运动能力。用育亨宾(1?mg / kg,ip,α 2 -肾上腺素受体拮抗剂),普萘洛尔(1?mg / kg,ip,β-肾上腺素受体拮抗剂),SCH23390(0.05?mg / kg,sc,多巴胺D 1 受体拮抗剂)或舒必利(50?mg / kg,ip,多巴胺D 2 受体拮抗剂)阻止了提取物的抗抑郁作用在FST(30?mg / kg)中。此外,酮色林(5?mg / kg,即优先的5-HT 2A 受体拮抗剂)增强了提取物在FST中的作用。讨论与结论:本研究结果表明,P。paniculata提取物具有抗抑郁样作用,可能是通过与5-羟色胺能(5-HT 2A 受体),去甲肾上腺素能相互作用而介导的。 (α 2 和β受体)和多巴胺能(D 1 和D 2 受体)系统。

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