Smith Dylan M, Fisher Derek, Blier Pierre, Illivitsky Vadim, Knott Verner
University of Ottawa Institute of Mental Health Research, 1145 Carling Ave., Ottawa, ON, Canada, K1Z 7K4,
Psychopharmacology (Berl). 2015 Jun;232(11):1911-20. doi: 10.1007/s00213-014-3823-8. Epub 2014 Dec 4.
The cognitive effects of nicotine in humans remain a topic of great interest, due to the continued prevalence of cigarette smoking in society as well as the hypothesis that cognitively impaired populations such as schizophrenia patients use nicotine as a means of self-medicating against deficits of sensory gating. However, chronic smoking can predispose individuals to robust monoamine oxidase (MAO) inhibition, and thus far, the effect of MAO inhibition on human sensory gating is unknown.
In this study, we investigated the effects of both nicotine (6-mg gum) and pharmacologically induced MAO-A inhibition via moclobemide (75 mg) on P50 event-related potential-indexed sensory gating in a sample of 24 healthy non-smoking males.
Ratio score (rP50) measured gating revealed significant improvement in auditory stimulus suppression after combined nicotine and MAO-A inhibition compared to placebo and to the nicotine-alone condition. This nicotine + MAO-A inhibition-induced efficient gating was consistent regardless of participants' baseline (placebo) gating efficiency, despite the observation that nicotine in the absence of MAO-A inhibition exhibited a detrimental effect on gating in participants with high baseline suppression ratios.
Nicotine and monoamine oxidase-inhibiting agents in tobacco smoke appear to exert a synergistic effect on sensory gating, which may contribute to the elevated dependence rates seen in populations with cognitive deficits such as schizophrenia.
由于社会中吸烟现象持续普遍,以及诸如精神分裂症患者等认知受损人群将尼古丁用作自我治疗感觉门控缺陷手段的假说,尼古丁对人类认知的影响仍是一个备受关注的话题。然而,长期吸烟会使个体易于出现强烈的单胺氧化酶(MAO)抑制作用,迄今为止,MAO抑制对人类感觉门控的影响尚不清楚。
在本研究中,我们调查了尼古丁(6毫克口香糖)和通过吗氯贝胺(75毫克)进行的药理学诱导的MAO-A抑制对24名健康非吸烟男性样本中P50事件相关电位索引的感觉门控的影响。
与安慰剂和单独使用尼古丁的情况相比,测量门控的比率分数(rP50)显示,联合使用尼古丁和MAO-A抑制后听觉刺激抑制有显著改善。无论参与者的基线(安慰剂)门控效率如何,这种尼古丁+MAO-A抑制诱导的有效门控都是一致的,尽管观察到在没有MAO-A抑制的情况下尼古丁对基线抑制率高的参与者的门控有不利影响。
烟草烟雾中的尼古丁和单胺氧化酶抑制剂似乎对感觉门控发挥协同作用,这可能导致在诸如精神分裂症等认知缺陷人群中出现较高的依赖率。