Trost Sarah, Diekhof Esther Kristina, Zvonik Kerstin, Lewandowski Mirjana, Usher Juliana, Keil Maria, Zilles David, Falkai Peter, Dechent Peter, Gruber Oliver
Department of Psychiatry and Psychotherapy, Centre for Translational Research in Systems Neuroscience and Clinical Psychiatry, Georg August University, Goettingen, Germany.
1] Department of Psychiatry and Psychotherapy, Centre for Translational Research in Systems Neuroscience and Clinical Psychiatry, Georg August University, Goettingen, Germany [2] Biocenter Grindeland Zoological Museum, Institute for Human Biology, University of Hamburg, Hamburg, Germany.
Neuropsychopharmacology. 2014 Jul;39(8):1914-23. doi: 10.1038/npp.2014.39. Epub 2014 Feb 18.
Bipolar disorder (BD) is characterized by recurrent mood episodes ranging from severe depression to acute full-blown mania. Both states of this severe psychiatric disorder have been associated with alterations of reward processing in the brain. Here, we present results of a functional magnetic resonance imaging (fMRI) study on the neural correlates and functional interactions underlying reward gain processing and reward dismissal in favor of a long-term goal in bipolar patients. Sixteen medicated patients diagnosed with bipolar I disorder, euthymic to mildly depressed, and sixteen matched healthy controls performed the 'desire-reason dilemma' (DRD) paradigm demanding rejection of priorly conditioned reward stimuli to successfully pursue a superordinate goal. Both groups exhibited significant activations in reward-related brain regions, particularly in the mesolimbic reward system. However, bipolar patients showed reduced neural responses of the ventral striatum (vStr) when exploiting a reward stimulus, and exhibited a decreased suppression of the reward-related activation of the mesolimbic reward system while having to reject immediate reward in favor of the long-term goal. Further, functional interaction between the anteroventral prefrontal cortex and the vStr in the 'DRD' was significantly impaired in the bipolar group. These findings provide evidence for a reduced responsivity of the vStr to reward stimuli in BD, possibly related to clinical features like anhedonia. The disturbed top-down control of mesolimbic reward signals by prefrontal brain regions in BD can be interpreted in terms of a disease-related enhanced impulsivity, a trait marker of BD.
双相情感障碍(BD)的特征是反复出现情绪发作,范围从严重抑郁到急性全面躁狂。这种严重精神疾病的两种状态都与大脑奖赏处理的改变有关。在此,我们展示了一项功能磁共振成像(fMRI)研究的结果,该研究针对双相情感障碍患者在奖赏获得处理和为了长期目标而摒弃奖赏背后的神经关联和功能相互作用。16名被诊断为双相I型障碍、处于情绪平稳至轻度抑郁状态的正在接受药物治疗的患者,以及16名匹配的健康对照者,进行了“欲望 - 理性困境”(DRD)范式实验,该实验要求拒绝先前已形成条件的奖赏刺激,以成功追求一个更高层次的目标。两组在与奖赏相关的脑区均表现出显著激活,尤其是在中脑边缘奖赏系统。然而,双相情感障碍患者在利用奖赏刺激时腹侧纹状体(vStr)的神经反应减弱,并且在不得不为了长期目标而拒绝即时奖赏时,对中脑边缘奖赏系统奖赏相关激活的抑制作用降低。此外,双相情感障碍组在“DRD”实验中前额叶腹侧前皮质与vStr之间的功能相互作用显著受损。这些发现为双相情感障碍中vStr对奖赏刺激的反应性降低提供了证据,这可能与快感缺失等临床特征有关。双相情感障碍中前额叶脑区对中脑边缘奖赏信号自上而下的控制受到干扰,可以用与疾病相关的冲动性增强来解释,冲动性增强是双相情感障碍的一个特质标记。