Anxiolytic and Sedative Effects of Extracts and Essential Oil from Citrus aurantium L.

抗焦虑药 镇静剂 抗惊厥药 药理学 高架加迷宫 戊巴比妥 化学 安定 氟马西尼 镇静 精油 催眠药 麻醉 医学 焦虑 癫痫 食品科学 苯二氮卓 生物化学 受体 精神科
作者
M.I.R. Carvalho-Freitas,Mirtes Costa
出处
期刊:Biological & Pharmaceutical Bulletin [Pharmaceutical Society of Japan]
卷期号:25 (12): 1629-1633 被引量:244
标识
DOI:10.1248/bpb.25.1629
摘要

Citrus aurantium L. is commonly used as an alternative treatment for insomnia, anxiety and epilepsy. Essential oil from peel (EOP) and hydroethanolic (70% w/v) extract (HE) from leaves were obtained. Hexanic (HF), dichloromethanic (DF) and final aqueous (AF) fractions were obtained from HE by successive partitions. Swiss male mice (35—45 g) were treated orally with 0.5 or 1.0 g/kg of these preparations 30 min before the experiments for the evaluation of the sedative/hypnotic activity (sleeping time induced by sodium pentobarbital – SPB: 40 mg/kg, i.p.), anxiolytic activity (elevated plus maze – EPM) and anticonvulsant activity (induced by pentylenetetrazole – PTZ: 85 mg/kg, sc or by maximal electroshock – MES: 50 mA, 0.11 s, corneal). The results showed that EOP (0.5 g/kg) increased the latency period of tonic seizures in both convulsing experimental models. This effect was not dose-dependent. Treatment with 1.0 g/kg increased the sleeping time induced by barbiturates and the time spent in the open arms of the EPM. Specific tests indicated that the preparation, in both doses used, did not promote deficits in general activity or motor coordination. HF and DF fractions (1.0 g/kg) did not interfere in the epileptic seizures, but were able to enhance the sleeping time induced by barbiturates. The results obtained with EOP in the anxiety model, and with EOP, HF and DF in the sedation model, are in accord with the ethnopharmacological use of Citrus aurantium L., which could be useful in primary medical care, after toxicological investigation.
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