α-细辛酮对小鼠抗精神病样活性的初步研究

V. Pandy
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引用次数: 3

摘要

α (α) -细辛酮是已知的活性化合物之一,已被发现是负责Acorus物种的治疗效益。已有研究报道菖蒲叶提取物对黑质纹状体多巴胺能系统具有神经调节作用。因此,本研究旨在研究α-细辛酮的抗精神病样活性,采用阿啡啡诱导的小鼠模型刻板行为。本研究采用瑞士白化雄性小鼠(体重25-30g)。在急性研究中,α-细辛酮分别以不同剂量(1、10、30、50、100 mg/kg体重)在阿波吗啡(5mg/kg, ig)注射前1小时口服。注射阿吗啡后立即将小鼠单独置于直径18 cm,高19 cm的圆柱形金属笼中,笼壁和笼底由垂直和水平金属条组成,记录小鼠的攀爬时间和攀爬行为。攀爬行为的评分为4 =四只爪子在笼壁上,2 =两只爪子在笼壁上,0 =四只爪子在地板上。α-细辛酮急性处理(1 ~ 100 mg/kg, p.o)在爬笼行为中表现出倒钟形剂量反应。α-asarone 30和50 mg/kg显著降低阿吗啡诱导小鼠爬笼时间和爬笼行为。这些作用可能与α-细辛酮的抗多巴胺能特性有关。多巴胺D2受体的拮抗作用是大多数临床有效的抗精神病药物的共同特征,特别是对幻觉和妄想有活性。总的来说,本研究揭示了α-细辛酮的抗多巴胺能作用;因此α-细辛酮在小鼠中表现出抗精神病样活性。然而,α-细辛酮作为一种新型抗精神病药物的作用机制有待进一步的神经化学研究。
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Antipsychotic-Like Activity of α-Asarone in Mice: A Preliminary Report
Alpha (α) - asarone is known to be one of the active compounds which have been discovered to be responsible for the therapeutic benefits of Acorus species. Previous studies have reported that Acorus calamus leaf extracts exerted the neuromodulatory effects on the nigrostriatal dopaminergic system. Therefore, the present study aimed to investigate the antipsychotic-like activity of α-asarone using a mouse model of apomorphine-induced stereotyped behaviour. Swiss albino male mice (bodyweight, 25-30g) were used for this study. In acute studies, α-asarone at different doses 1, 10, 30, 50, and 100 mg/kg bodyweight were administered orally one hour prior to apomorphine (5mg/kg, i.p.) injection respectively. Immediately after the injection of apomorphine, the mice were placed individually in cylindrical metal cages (18 cm in diameter and 19 cm in height) with the wall and floor consisting of vertical and horizontal metal bars and recorded for climbing time and climbing behaviour. The climbing behaviour was scored as 4 = four paws on the wall of the cage, 2 = two paws on the wall of the cage, 0 = four paws on the floor. The acute treatment of α-asarone (1-100 mg/kg, p.o.) exhibited an inverted bell-shaped dose-response in cage climbing behaviour. α-asarone at 30 and 50 mg/kg significantly decreased the apomorphine-induced cage climbing time and climbing behaviour in mice. These observed effects might be attributed due to the antidopaminergic property of α-asarone. Antagonism of dopamine D2 receptors is a common feature of the most clinically effective antipsychotic drugs, especially active against hallucinations and delusions. Overall, the present study uncovered the antidopaminergic effect of α-asarone; thereby α-asarone exhibited antipsychotic-like activity in mice. However, further neurochemical studies are warranted to explore the actual mechanism of action of α-asarone as a promising novel antipsychotic agent.
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