非典型意识改变和精神病的Kappa阿片模型:U50488, DOI, AC90179对小鼠脉搏前抑制和运动的影响。

Journal of young investigators Pub Date : 2009-07-01
Michael A Ruderman, Susan B Powell, Mark A Geyer
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引用次数: 0

摘要

感觉控制门控和运动行为分别反映了注意前感觉过滤和高阶自上而下的感觉加工。这些过程被认为会影响环境中对新颖性的感知(过滤)或认知(高阶处理),这是意识改变状态模型(ASC)的显著特征。具有高选择性受体亲和力的药物可产生ASC,有助于建立ASC的神经关联、通路和机制。此外,筛选选择性逆转药物诱导的感觉处理偏离的物质对实验性抗精神病药物的开发是有价值的。本研究调查了两种ASC模型中的异常阿片亚型kappa阿片(KA)系统。在三个BPM测量中观察到KA与血清素/2A (5-HT2A)系统(与经典迷幻药相关的血清素亚型)之间的显著相互作用和逆转效应。这些测量表明,KA激活诱导的效应可以通过5-HT2A失活来逆转。这些结果表明KA可以作为一种非典型抗精神病药物和/或作为新的抗精神病药物的筛选工具。本研究的实验工作包括剂量反应和逆转实验,首次在小鼠的两种行为模型中使用药物激活和停用kappa阿片样物质和血清素系统。
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A Kappa Opioid Model of Atypical Altered Consciousness and Psychosis: U50488, DOI, AC90179 Effects on Prepulse Inhibition and Locomotion in Mice.

Sensorimortor gating and locomotion are behaviors that reflect pre-attentive sensory filtering and higher order, top-down, sensory processing, respectively. These processes are thought to affect either the perception of novelty in an environment (filtering) or cognition (higher order processing), salient features of models of altered states of consciousness (ASC). Drugs with highly selective receptor affinities that produce ASC can help to establish neural correlates, pathways, and mechanisms underlying ASC. Furthermore, screening for substances that selectively reverse drug-induced sensory processing departures is valuable for development of experimental antipsychotics. This study investigated the anomalous opioid sub-type, the kappa opioid (KA) system, within the two ASC models. Significant interaction and reversal effects between KA and the serotonin/2A (5-HT2A) system - the serotonin sub-type associated with classical psychedelics - were observed in three BPM measures. These measures showed that KA activation-induced effects could be reversed by 5-HT2A deactivation. These results suggest that KA could function as an atypical antipsychotic medications and/or as a screening tool for new antipsychotic medicines. The experimental work for this study comprised dose-response and reversal experiments with drugs that activate and deactivate kappa opioid and serotonin systems in the two behavioral models for the first time in mice.

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