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A low dosage of the dopamine D2-receptor antagonist sulpiride affects effort allocation for reward regardless of trait extraversion

机译:低剂量的多巴胺D2受体拮抗剂舒必利会影响奖励分配的努力而与性格外向性无关

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摘要

Dopamine (DA) is known to be involved in various aspects of reward processing and goal-directed behavior. The present preregistered study aims at directly accessing the causal influence of DA activity on reward motivation in humans, while also accounting for trait extraversion. Therefore, we examined the effect of a single dose of the DA D2 receptor antagonist sulpiride (200 mg) on effort allocation in a modified version of the Effort-Expenditure for Reward Task (EEfRT). Based on its presumably DA increasing action, we expected the low dose of sulpiride to increase participants’ willingness to allocate effort during the modified EEfRT relative to placebo, especially in trials with low probability of reward attainment. Further, we expected a moderating effect of trait extraversion on the effects of sulpiride. Two hundred and three healthy male participants were tested in a randomized, double-blind between-subjects design. Contrary to our expectations, sulpiride reduced the average number of clicks within the modified EEfRT and did not interact with reward attributes, suggesting a more global and not reward-specific effect of sulpiride. Furthermore, trait extraversion did not moderate the effect of sulpiride. Our results provide initial support for the validity of the modified version of the EEfRT, suggesting a possible inhibiting effect of a low dose of sulpiride on approach motivation regardless of trait extraversion. However, given the mixed pattern of findings and the possible confounding role of motoric abilities, further studies examining these effects are clearly warranted.
机译:众所周知,多巴胺(DA)涉及奖励处理和目标导向行为的各个方面。本预先注册的研究旨在直接获得DA活动对人类奖励动机的因果影响,同时也考虑特质外向性。因此,我们在改良版的“用于奖励任务的支出”(EEfRT)中检查了单剂量DA D2受体拮抗剂舒必利(200 mg)对精力分配的影响。基于其可能增加DA的作用,我们期望低剂量的舒必利可以提高参与者在改良EEfRT期间相对于安慰剂分配工作的意愿,尤其是在获得奖励可能性较低的试验中。此外,我们预期性状外向性对舒必利的影响会产生调节作用。在随机,双盲受试者间设计中对203名健康男性参与者进行了测试。与我们的预期相反,舒必利降低了改良版EEfRT中的平均点击次数,并且未与奖励属性交互作用,这表明舒必利具有更广泛的全球效应,而不是针对奖励的作用。此外,性状外向性不能减轻舒必利的作用。我们的结果为EEfRT修改版的有效性提供了初步支持,表明低剂量舒必利可能对进阶动机产生抑制作用,而与性格外向性无关。然而,鉴于发现的混合模式和运动能力的可能混杂作用,显然有必要进一步研究这些作用。

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