Volman Inge, Pringle Abbie, Verhagen Lennart, Browning Michael, Cowen Phil J, Harmer Catherine J
Oxford Health NHS Foundation Trust, Warneford Hospital, Oxford, UK.
Department of Psychiatry, University of Oxford, Oxford, UK.
Neuropsychopharmacology. 2021 Jan;46(2):386-393. doi: 10.1038/s41386-020-00895-2. Epub 2020 Oct 30.
Lithium is one of the most effective mood-stabilizing medications in bipolar disorder. This study was designed to test whether lithium administration may stabilize mood via effects on reward processing. It was hypothesized that lithium administration would modulate reward processing in the striatum and affect both anticipation and outcome computations. Thirty-seven healthy human participants (18 males, 33 with suitable fMRI data) received 11 (±1) days of lithium carbonate or placebo intervention (double-blind), after which they completed the monetary incentive delay task while fMRI data were collected. The monetary incentive delay task is a robust task with excellent test-retest reliability and is well suited to investigate different phases of reward processing within the caudate and nucleus accumbens. To test for correlations with prediction error signals a Rescorla-Wagner reinforcement-learning model was applied. Lithium administration enhanced activity in the caudate during reward anticipation compared to placebo. In contrast, lithium administration reduced caudate and nucleus accumbens activity during reward outcome. This latter effect seems related to learning as reward prediction errors showed a positive correlation with caudate and nucleus accumbens activity during placebo, which was absent after lithium administration. Lithium differentially modulates the anticipation relative to the learning of rewards. This suggests that lithium might reverse dampened reward anticipation while reducing overactive reward updating in patients with bipolar disorder. This specific effect of lithium suggests that a targeted modulation of reward learning may be a viable approach for novel interventions in bipolar disorder.
锂是双相情感障碍中最有效的心境稳定剂之一。本研究旨在测试锂的给药是否可能通过对奖赏加工的影响来稳定情绪。研究假设锂的给药会调节纹状体中的奖赏加工,并影响预期和结果计算。37名健康人类参与者(18名男性,33名有合适的功能磁共振成像数据)接受了11(±1)天的碳酸锂或安慰剂干预(双盲),之后他们在收集功能磁共振成像数据的同时完成了金钱激励延迟任务。金钱激励延迟任务是一项稳健的任务,具有出色的重测信度,非常适合研究尾状核和伏隔核内奖赏加工的不同阶段。为了测试与预测误差信号的相关性,应用了雷斯克拉-瓦格纳强化学习模型。与安慰剂相比,锂的给药增强了奖赏预期期间尾状核的活动。相反,锂的给药降低了奖赏结果期间尾状核和伏隔核的活动。后一种效应似乎与学习有关,因为奖赏预测误差在安慰剂期间与尾状核和伏隔核的活动呈正相关,而在锂给药后这种相关性消失。锂相对于奖赏学习对预期进行差异性调节。这表明锂可能会逆转双相情感障碍患者中减弱的奖赏预期,同时减少过度活跃的奖赏更新。锂的这种特定效应表明,针对性地调节奖赏学习可能是双相情感障碍新型干预措施的一种可行方法。