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普瑞巴林对诱发海马θ振荡的抗焦虑作用

Anxiolytic profile of pregabalin on elicited hippocampal theta oscillation.

作者信息

Siok Chester J, Taylor Charles P, Hajós Mihály

机构信息

Department of Neuroscience, Pfizer Global Research and Development, Eastern Point Road, Groton, CT 06340, USA.

出版信息

Neuropharmacology. 2009 Feb;56(2):379-85. doi: 10.1016/j.neuropharm.2008.09.013. Epub 2008 Oct 7.

Abstract

Previous published work with the novel anticonvulsant, analgesic and anti-anxiety medication, pregabalin (Lyrica), has shown that it has anxiolytic-like actions in several animal behavioral models. However, pregabalin is structurally and pharmacologically different from other classes of known anxiolytic drugs, and the mechanisms that alter brain activity to produce anxiolytic-like actions are not well understood. In an effort to determine more about the cellular mechanisms of pregabalin, we studied its effects on hippocampal theta activity of urethane-anesthetized rats that was elicited by electrical stimulation of the nucleus pontis oralis (nPO) in the brainstem. We found that systemic administration of pregabalin significantly reduced the frequency of stimulation-induced hippocampal theta activity similarly to the effects of diazepam. In addition, pregabalin (but not diazepam) significantly altered the stimulus intensity/frequency relationship, and increased slow delta oscillation (<3.0Hz) in spontaneous hippocampal EEG in a dose-dependent manner. Our findings suggest that pregabalin may alter evoked theta frequency activity in the hippocampus by reducing neurotransmitter-mediated activation of either the septal nucleus or the hippocampus, and that its actions are unlikely to be mediated by direct activation of GABA neurotransmitter systems. These observations provide further insight to the action of pregabalin, and support the utilization of stimulation-induced theta model in discovery of novel anxiolytic drugs.

摘要

先前发表的关于新型抗惊厥、镇痛和抗焦虑药物普瑞巴林(乐瑞卡)的研究表明,它在多种动物行为模型中具有抗焦虑样作用。然而,普瑞巴林在结构和药理上与其他已知抗焦虑药物不同,其改变大脑活动以产生抗焦虑样作用的机制尚不清楚。为了更多地了解普瑞巴林的细胞机制,我们研究了它对经脑干脑桥嘴侧核(nPO)电刺激诱发的、乌拉坦麻醉大鼠海马θ活动的影响。我们发现,与地西泮的作用相似,全身给予普瑞巴林可显著降低刺激诱发的海马θ活动频率。此外,普瑞巴林(而非地西泮)显著改变了刺激强度/频率关系,并以剂量依赖的方式增加了海马自发脑电图中的慢δ振荡(<3.0Hz)。我们的研究结果表明,普瑞巴林可能通过减少隔核或海马的神经递质介导的激活来改变海马中诱发的θ频率活动,并且其作用不太可能由GABA神经递质系统的直接激活介导。这些观察结果为普瑞巴林的作用提供了进一步的见解,并支持在新型抗焦虑药物发现中利用刺激诱发的θ模型。

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