Pharmacology and Anaesthesiology Unit, School of Medicine and Pharmacology, The University of Western Australia, Australia.
J Psychiatry Neurosci. 2013 Jan;38(1):24-32. doi: 10.1503/jpn.110145.
An emerging endophenotype of schizophrenia is the reduction of both power and phase locking of the 40 Hz auditory steady state response (ASSR), and there have been a number of reports linking increased γ activity with positive psychotic symptoms. Schizophrenia and, more specifically, positive psychotic symptoms have been closely linked to increased dopamine (DA) neurophysiology. Therefore, we gave dexamphetamine to healthy participants to determine the effect that increased DA transmission would have on the ASSR.
We administered 0.45 mg/kg of dexamphetamine orally in a double-blind placebo-controlled crossover study. Stimuli were 20 Hz and 40 Hz click trains presented in an auditory oddball-type stimulus format (probability of stimulus presentation: 0.2 for targets, 0.8 for nontargets).
We included 44 healthy volunteers (18 women) in the study. Dexamphetamine significantly increased the 40 Hz power for both target and nontarget ASSR stimuli. Dexamphetamine did not significantly affect the 40 Hz phase-locking factor (PLF) or the 20 Hz power and PLF. Whereas there were significant effects of selective attention on power and PLF for 20 and 40 Hz ASSR, there were no significant interactions between dexamphetamine and selective attention.
Dexamphetamine releases both noradrenaline and DA with equal potency. Further research with selective dopaminergic and noradrenergic agents will better characterize the effects of monoamines on γ activity.
The results demonstrate a frequency-specific effect of dexamphetamine on the ASSR. This finding is consistent with previous research that has found an association between increased γ and positive symptoms of psychosis. However, this result also raises the possibility that previous 40 Hz ASSR findings in people with schizophrenia may be confounded by effects of antipsychotic medication. Possible neural mechanisms by which dexamphetamine specifically increases 40 Hz power are also discussed. AUSTRALIAN AND NEW ZEALAND CLINICAL TRIALS REGISTRY NUMBER: ACTRN12608000610336.
精神分裂症的一个新兴内表型是 40Hz 听觉稳态响应(ASSR)的功率和相位锁定的降低,并且有许多报告将γ活动增加与阳性精神病症状联系起来。精神分裂症,更具体地说,阳性精神病症状与多巴胺(DA)神经生理学的增加密切相关。因此,我们给健康参与者服用右苯丙胺,以确定增加 DA 传递对 ASSR 的影响。
我们在一项双盲安慰剂对照交叉研究中口服给予 0.45mg/kg 的右苯丙胺。刺激物是 20Hz 和 40Hz 的点击列车,以听觉异类刺激格式呈现(刺激呈现的概率:目标为 0.2,非目标为 0.8)。
我们纳入了 44 名健康志愿者(18 名女性)参与研究。右苯丙胺显著增加了目标和非目标 ASSR 刺激物的 40Hz 功率。右苯丙胺对 40Hz 相位锁定因子(PLF)或 20Hz 功率和 PLF 没有显著影响。虽然选择性注意对 20Hz 和 40Hz ASSR 的功率和 PLF 有显著影响,但右苯丙胺和选择性注意之间没有显著的相互作用。
右苯丙胺以同等效力释放去甲肾上腺素和 DA。进一步研究选择性多巴胺能和去甲肾上腺素能药物将更好地描述单胺对γ活性的影响。
结果表明右苯丙胺对 ASSR 有频率特异性影响。这一发现与先前的研究一致,即发现增加的γ与精神病阳性症状之间存在关联。然而,这一结果也提出了一个可能性,即以前在精神分裂症患者中发现的 40Hz ASSR 结果可能受到抗精神病药物的影响。还讨论了右苯丙胺特异性增加 40Hz 功率的可能神经机制。澳大利亚和新西兰临床试验注册编号:ACTRN12608000610336。