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一种简单的含硒分子,甲基苯硒醚,在小鼠体内的抗抑郁作用。

The antidepressant-like action of a simple selenium-containing molecule, methyl phenyl selenide, in mice.

机构信息

Laboratório de Síntese, Reatividade e Avaliação Farmacológica e Toxicológica de Organocalcogênios, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria CEP 97105-900, RS, Brazil.

出版信息

Eur J Pharmacol. 2012 Sep 5;690(1-3):119-23. doi: 10.1016/j.ejphar.2012.06.009. Epub 2012 Jun 16.

DOI:10.1016/j.ejphar.2012.06.009
PMID:22713547
Abstract

Selenium-containing molecules show promising pharmacological properties. The antidepressant-like action of CH(3)SePh in the mouse forced swimming test (FST) and the tail suspension test (TST), models predictive of depressant activity, were investigated in this study. Moreover, the involvement of dopaminergic system in the antidepressant-like action of CH(3)SePh was studied. The behavioral results showed that CH(3)SePh significantly reduced the immobility time in the FST (25 and 50 mg/kg, intragastrically; i.g.) and the TST (50 mg/kg, i.g.), without accompanying changes in ambulation when assessed in the open-field test (OFT). The anti-immobility effect of CH(3)SePh (50 mg/kg, intragastrically; i.g.) in the FST was prevented by pretreatment of mice with haloperidol (0.2 mg/kg, i.p., a dopamine D(2) receptor antagonist), SCH 23390 (R-(+)-8-chloro-2,3,4,5-tetrahydro-3-methyl-5-phenyl-1H-3-benzazepine-7-ol) (0.05 mg/kg, s.c., a dopamine D(1) receptor antagonist) and sulpiride (50 mg/kg, i.p., a dopamine D(2) and D(3) antagonist). These results suggest that CH(3)SePh produced an antidepressant-like action in the mouse FST and TST. The antidepressant-like action of CH(3)SePh, a simple selenium-containing molecule, seems most likely to be mediated through an interaction with the dopaminergic system.

摘要

含硒分子显示出有前景的药理学特性。本研究旨在探讨 CH(3)SePh 在小鼠强迫游泳试验(FST)和悬尾试验(TST)中的抗抑郁样作用,这两种模型可预测抗抑郁活性。此外,还研究了多巴胺能系统在 CH(3)SePh 抗抑郁样作用中的参与情况。行为学结果表明,CH(3)SePh 可显著减少 FST(25 和 50mg/kg,灌胃;i.g.)和 TST(50mg/kg,i.g.)中的不动时间,而在开放场试验(OFT)中评估时,对运动没有伴随变化。CH(3)SePh(50mg/kg,灌胃;i.g.)在 FST 中的抗不动作用可被氟哌啶醇(0.2mg/kg,腹腔注射,多巴胺 D2 受体拮抗剂)、SCH 23390(R-(+)-8-氯-2,3,4,5-四氢-3-甲基-5-苯基-1H-3-苯并氮杂卓-7-醇)(0.05mg/kg,皮下注射,多巴胺 D1 受体拮抗剂)和舒必利(50mg/kg,腹腔注射,多巴胺 D2 和 D3 拮抗剂)预处理的小鼠所阻止。这些结果表明,CH(3)SePh 在小鼠 FST 和 TST 中产生了抗抑郁样作用。CH(3)SePh 是一种简单的含硒分子,其抗抑郁样作用似乎最有可能通过与多巴胺能系统相互作用介导。

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