金钱奖惩过程中多巴胺合成的功能动力学。

Andreas Hahn, Murray B Reed, Verena Pichler, Paul Michenthaler, Lucas Rischka, Godber M Godbersen, Wolfgang Wadsak, Marcus Hacker, Rupert Lanzenberger
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引用次数: 0

摘要

PET竞争模型对多巴胺释放的评估已得到充分验证,但对认知过程的研究存在不足。我们介绍了一种新的方法,将6-[18F]FDOPA摄取作为神经元放电对多巴胺合成酶动态调节的指标。通过评估多巴胺神经传递中广泛描述的性别差异,证明了这种方法的可行性。在36名健康参与者中,有16人在金钱激励延迟任务中完成了fPET和fMRI。单次50分钟fPET采集6-[18F]FDOPA用于量化多巴胺合成的任务特异性变化。在男性中,金钱收益比金钱损失更能引起腹侧纹状体多巴胺合成的增加。有趣的是,在女性身上发现了相反的效果。这些变化与奖励(男性)和惩罚敏感性(女性)进一步相关。正如预期的那样,fMRI显示了强大的任务特异性神经元激活,但没有性别差异。我们的研究结果为奖惩处理中已知的行为性别差异提供了神经生物学基础,对精神疾病的性别特异性患病率、奖励处理和多巴胺信号的改变具有重要意义。高时间分辨率和任务特异性变化的大小使fPET成为研究认知加工和大脑疾病过程中功能性神经递质动力学的有前途的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Functional dynamics of dopamine synthesis during monetary reward and punishment processing.

Functional dynamics of dopamine synthesis during monetary reward and punishment processing.

Functional dynamics of dopamine synthesis during monetary reward and punishment processing.

Functional dynamics of dopamine synthesis during monetary reward and punishment processing.

The assessment of dopamine release with the PET competition model is thoroughly validated but entails disadvantages for the investigation of cognitive processes. We introduce a novel approach incorporating 6-[18F]FDOPA uptake as index of the dynamic regulation of dopamine synthesis enzymes by neuronal firing. The feasibility of this approach is demonstrated by assessing widely described sex differences in dopamine neurotransmission. Reward processing was behaviorally investigated in 36 healthy participants, of whom 16 completed fPET and fMRI during the monetary incentive delay task. A single 50 min fPET acquisition with 6-[18F]FDOPA served to quantify task-specific changes in dopamine synthesis. In men monetary gain induced stronger increases in ventral striatum dopamine synthesis than loss. Interestingly, the opposite effect was discovered in women. These changes were further associated with reward (men) and punishment sensitivity (women). As expected, fMRI showed robust task-specific neuronal activation but no sex difference. Our findings provide a neurobiological basis for known behavioral sex differences in reward and punishment processing, with important implications in psychiatric disorders showing sex-specific prevalence, altered reward processing and dopamine signaling. The high temporal resolution and magnitude of task-specific changes make fPET a promising tool to investigate functional neurotransmitter dynamics during cognitive processing and in brain disorders.

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