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静息态动力学可作为健康成年女性中多巴胺给药的神经生物标志物。

Resting-state dynamics as a neuromarker of dopamine administration in healthy female adults.

机构信息

1 Department of Psychology I, University of Lübeck, Lübeck, Germany.

2 Decision Neuroscience and Nutrition, German Institute of Human Nutrition (DIfE), Nuthetal, Germany.

出版信息

J Psychopharmacol. 2019 Aug;33(8):955-964. doi: 10.1177/0269881119855983. Epub 2019 Jun 27.

Abstract

BACKGROUND

Different neuromarkers of people's emotions, personality traits and behavioural performance have recently been identified. However, not much attention has been devoted to neuromarkers of neural responsiveness to drug administration.

AIMS

We investigated the predictive neuromarkers of acute dopamine (DA) administration.

METHODS

In a double-blind, within-subject study, we administrated a DA agonist (pramipexole) or placebo to 27 healthy female subjects. Using multivariate classification and prediction analyses, we examined whether dopaminergic modulations of task-free resting-state brain dynamics predict individual differences in pramipexole's modulation of facial attractiveness evaluations.

RESULTS

Our results demonstrate that pramipexole's effects on brain dynamics could be successfully discriminated from resting-state functional connectivity (accuracy: 78.9%; < 0.0001). On the behavioural level, pramipexole increased facial attractiveness evaluations ( = 4.44; < 0.0001). In particular, pramipexole administration enhanced connectivity strength of the cinguloopercular network ( = 3.29; = 0.003) and increased brain signal variability in subcortical and prefrontal brain areas ( = 3.05, = 0.009). Importantly, multivariate predictive models reveal that pramipexole-dependent modulation of resting-state dynamics predicted the increase of facial attractiveness evaluations after pramipexole (connectivity strength: standardized mean squared error, = 0.65; = 0.0007; brain signal variability: = 0.94, = 0.015).

CONCLUSION

These results demonstrate that modulations of resting-state brain dynamics induced by a DA agonist predict drug-related effects on evaluation processes, providing a neuromarker of the neural responsiveness of specific brain networks to DA administration.

摘要

背景

最近已经确定了人们情绪、个性特征和行为表现的不同神经标志物,但对药物给药后神经反应性的神经标志物关注较少。

目的

我们研究了急性多巴胺(DA)给药的预测神经标志物。

方法

在一项双盲、自身对照研究中,我们给 27 名健康女性受试者给予 DA 激动剂(普拉克索)或安慰剂。使用多元分类和预测分析,我们检验了任务态静息态脑动力学的多巴胺调制是否可以预测普拉克索对面部吸引力评估的调制的个体差异。

结果

我们的结果表明,普拉克索对脑动力学的影响可以与静息态功能连接成功区分(准确率:78.9%;<0.0001)。在行为水平上,普拉克索增加了面部吸引力评估(=4.44;<0.0001)。特别是,普拉克索给药增强了扣带-前运动网络的连接强度(=3.29;=0.003),并增加了皮质下和前额叶脑区的脑信号变异性(=3.05;=0.009)。重要的是,多元预测模型表明,静息态动力学的普拉克索依赖性调制预测了普拉克索后面部吸引力评估的增加(连接强度:标准化均方误差,=0.65;=0.0007;脑信号变异性:=0.94;=0.015)。

结论

这些结果表明,DA 激动剂诱导的静息态脑动力学的调制预测了药物对评估过程的影响,为特定脑网络对 DA 给药的神经反应性提供了神经标志物。

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