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Frobose, M. I.

Publications and source records attributed to Frobose, M. I..

3 recordsLinked to original sources

Dopaminergic and Cholinergic Modulation of Human Cost-Benefit Decision Making

In everyday life, we encounter situations that require tradeoffs between potential rewards and associated costs, such as time and (physical) effort. The literature indicates a prominent role for dopamine in discounting of both delay and effort, with mixed findings for delay discounting in humans. Moreover, the reciprocal antagonistic interaction between dopaminergic and cholinergic transmission in the striatum suggests a potential opponent role of acetylcholine in these processes. We found opposing effects of dopamine D2 (haloperidol) and acetylcholine M1 receptor (biperiden) antagonism on specific components of effort-based decision making in healthy humans: haloperidol decreased, whereas biperiden increased the willingness to exert physical effort. In contrast, delay discounting was reduced under haloperidol, but not affected by biperiden. Together, our data suggest that dopamine, acting at D2 receptors, modulates both effort and delay discounting, while acetylcholine, acting at M1 receptors, appears to exert a more specific influence on effort discounting only.

neuroscience↗

Catecholamine Challenge Uncovers Distinct Mechanisms For Direct Versus Indirect, But Not Social Versus Non-Social, Learning

Evidence that social and individual learning are at least partially dissociable sustains the belief that humans possess adaptive specialisations for social learning. However, in most extant paradigms, social information comprises an indirect source that can be used to supplement ones own, direct, experience. Thus, social and individual learning differ both in terms of social nature (social versus non-social) and directness (indirect versus direct). To test whether the dissociation between social and individual learning is best explained in terms of social nature or directness, we used a catecholaminergic challenge known to modulate learning. Two groups completed a decision-making task which required direct learning, from own experience, and indirect learning from an additional source. The groups differed in terms of whether the indirect source was social or non-social. The catecholamine transporter blocker, methylphenidate, affected direct learning by improving adaptation to changes in the volatility of the environment but there was no effect of methylphenidate on learning from the social or non-social indirect source. Thus, we report positive evidence for a dissociable effect of methylphenidate on direct and indirect learning, but no evidence for a distinction between social and non-social. These data fail to support the adaptive specialisation view, instead providing evidence for distinct mechanisms for direct versus indirect learning.

neuroscience↗

Catecholaminergic modulation of the avoidance of cognitive control

The catecholamines have long been associated with cognitive control and value-based decision-making. More recently, we proposed that the catecholamines might modulate value-based decision-making about whether or not to engage in cognitive control. We test this hypothesis by assessing effects of a catecholamine challenge in a large sample of young, healthy adults (n = 100) on the avoidance of a cognitively demanding control process: task switching. Prolonging catecholamine transmission by blocking reuptake with methylphenidate altered the avoidance, but not the execution of cognitive control. Crucially, these effects could be isolated by taking into account individual differences in trait impulsivity, so that participants with higher trait impulsivity became more avoidant of cognitive control, despite faster task performance. One implication of these findings is that performance-enhancing effects of methylphenidate may be accompanied by an undermining effect on the willingness to exert cognitive control. Taken together, these findings integrate hitherto segregated literatures on catecholamines roles in value-based learning/choice and cognitive control.

neuroscience↗