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The role of 5-HT1a and 5-HT2a receptors in attention and motor control: a mechanistic study in healthy volunteers.

机译:5-HT1a和5-HT2a受体在注意力和运动控制中的作用:在健康志愿者中的机制研究。

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RATIONALE: Various studies have demonstrated a modulating role for serotonin in attention. Selective serotonin inhibitors have repeatedly been shown to impair performance in sustained attention tasks. OBJECTIVES: To assess the contribution of serotonin reuptake inhibition and specific blockade of the pre-synaptic 5-HT(1a) receptor and the 5-HT(2a) receptor to deficits in attention. MATERIALS AND METHODS: The study was conducted according to a randomized, double-blind, placebo controlled, four-way crossover design including 16 healthy volunteers. Treatments consisted of oral administration of the selective serotonin reuptake inhibitor (SSRI) escitalopram 20 mg + placebo; escitalopram 20 mg + ketanserin (5-HT(2a) antagonist), 50 mg; escitalopram 20 mg + pindolol (5-HT(1a) antagonist) 10 mg; and placebo + placebo on four separate days. A range of performance tasks were conducted to assess the subjects' attention and motor functions. RESULTS: Escitalopram administered alone impaired tracking performance ina divided attention task. The combination of escitalopram and pindolol and escitalopram and ketanserin impaired divided attention as compared to placebo. In addition, escitalopram and ketanserin impaired sustained attention. Divided attention impairment observed after combined treatments did not significantly differ from impairments after escitalopram alone. Sustained attention impairment observed after combined escitalopram and ketanserin significantly differed from escitalopram alone. CONCLUSIONS: 5HT(1a) blockade hardly affected SSRI effects on attention. Additional 5HT(2a) blockade, however, produced impairments of sustained attention and motor impulse control.
机译:理由:各种研究表明5-羟色胺在注意力中的调节作用。选择性5-羟色胺抑制剂已被反复证明会损害持续注意力任务的表现。目的:评估5-羟色胺再摄取抑制和突触前5-HT(1a)受体和5-HT(2a)受体特异性阻滞对注意力缺陷的贡献。材料与方法:该研究是根据随机,双盲,安慰剂对照,四向交叉设计进行的,其中包括16名健康志愿者。治疗包括口服选择性5-羟色胺再摄取抑制剂(SSRI)依他普仑20 mg +安慰剂。依他普仑20毫克+酮色林(5-HT(2a)拮抗剂),50毫克;依他普仑20毫克+品多洛尔(5-HT(1a)拮抗剂)10毫克;和安慰剂+安慰剂分别在四天内进行。进行了一系列表演任务以评估受试者的注意力和运动功能。结果:单独服用艾司西酞普兰会损害分散注意力任务的追踪性能。与安慰剂相比,艾司西酞普兰和品多洛尔和艾司西酞普兰和酮色林的组合损害了注意力分散。此外,依西酞普兰和酮色林损害了持续的注意力。联合治疗后观察到的分散注意力障碍与单用依西酞普兰后的注意力障碍没有显着差异。依他普仑和酮色林联合使用后,观察到的持续注意力障碍明显不同于单独使用依他普仑。结论:5HT(1a)阻滞剂几乎不会影响SSRI对注意力的影响。但是,额外的5HT(2a)封锁会导致持续注意力和运动冲动控制受损。

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