Acute effects of mecamylamine and varenicline on cognitive performance in non-smokers with and without schizophrenia

麦加明 伐尼克兰 烟碱激动剂 精神分裂症(面向对象编程) 心理学 尼古丁 安慰剂 医学 戒烟 药理学 精神科 内科学 受体 替代医学 病理
作者
Sungwon Roh,Susanne S. Hoeppner,David Schoenfeld,Catherine A. Fullerton,Luke E. Stoeckel,A. Eden Evins
出处
期刊:Psychopharmacology [Springer Nature]
卷期号:231 (4): 765-775 被引量:23
标识
DOI:10.1007/s00213-013-3286-3
摘要

Nicotinic acetylcholine receptors (nAChRs) have been implicated in the pathophysiology of cognitive deficits in the domains of attention and memory in schizophrenia. While nicotinic agonists and antagonists have been proposed as smoking cessation aids, few comparisons have been made of these agents on cognitive performance in individuals with schizophrenia. This study investigated the acute effects of a nAChR antagonist, mecamylamine, and partial agonist, varenicline, on cognitive function in non-smokers with and without schizophrenia. Single oral doses of mecamylamine 10 mg, varenicline 1 mg, and placebo were administered 1 week apart in random order to adults with schizophrenia (n = 30) and to healthy volunteers (n = 41) in a double-blind, crossover design. The primary outcome of interest was sustained attention as assessed with hit reaction time variability (HRT-SD) on the identical pairs continuous performance test (CPT-IP). Mecamylamine worsened performance on CPT-IP HRT-SD, a measure of attention, compared to varenicline in both groups. Performance on mecamylamine was worse than performance on both placebo and varenicline on several additional measures of attention, including CPT-IP hit reaction time (HRT) and random errors at various levels of task difficulty. There was a treatment by diagnosis interaction, such that mecamylamine worsened performance on CPT-IP 2-digit HRT, 3-digit random errors, and 4-digit hit rate compared to placebo and varenicline in participants with schizophrenia; effects not observed in controls. These findings support a role for nAChRs in attention and suggest that those with schizophrenia may be particularly sensitive to nAChR blockade.
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