Key result
Methylphenidate reverses decreased midbrain error activity during mental fatigue in cocaine abusers.
Why the study?
Dopamine modulates executive function and sustaining cognitive control during mental fatigue, but its involvement in cocaine addiction during mental fatigue is unclear.
Does methylphenidate alter midbrain fMRI activity during mental fatigue in cocaine abusers and healthy controls?
Observational (n=82)
Double-blind (for methylphenidate subset)
Counterbalanced (for methylphenidate subset)
No
Does methylphenidate alter midbrain fMRI activity during mental fatigue in cocaine abusers and healthy controls?
The dopaminergic midbrain is involved in sustaining motivation during mental fatigue, and its aberrant response in cocaine addiction can be modulated by methylphenidate.
Answers are grounded in this paper and cite their sources.
Methylphenidate may normalize midbrain error responses during fatigue in cocaine users; hypothesis-generating and should not yet alter practice.
Dopamine modulates executive function, including sustaining cognitive control during mental fatigue. Using event-related functional magnetic resonance imaging (fMRI) during the color-word Stroop task, we aimed to model mental fatigue with repeated task exposures in 33 cocaine abusers and 20 healthy controls. During such mental fatigue (indicated by increased errors, and decreased post-error slowing and dorsal anterior cingulate response to error as a function of time-on-task), healthy individuals showed increased activity in the dopaminergic midbrain to error. Cocaine abusers, characterized by disrupted dopamine neurotransmission, showed an opposite pattern of response. This midbrain fMRI activity with repetition was further correlated with objective indices of endogenous motivation in all subjects: a state measure (task reaction time) and a trait measure (dopamine D2 receptor availability in caudate, as revealed by positron emission tomography data collected in a subset of this sample, which directly points to a contribution of dopamine to these results). In a second sample of 14 cocaine abusers and 15 controls, administration of an indirect dopamine agonist, methylphenidate, reversed these midbrain responses in both groups, possibly indicating normalization of response in cocaine abusers because of restoration of dopamine signaling but degradation of response in healthy controls owing to excessive dopamine signaling. Together, these multimodal imaging findings suggest a novel involvement of the dopaminergic midbrain in sustaining motivation during fatigue. This region might provide a useful target for strengthening self-control and/or endogenous motivation in addiction.
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Moeller et al. (2012) conducted an observational in Cocaine addiction and mental fatigue (n=82). Repeated task exposures (mental fatigue) vs. Healthy controls was evaluated on Midbrain fMRI BOLD response to error as a function of time-on-task (repetition × group interaction) (p=0.026). During mental fatigue induced by repeated task exposures, healthy individuals showed increased dopaminergic midbrain activity to error, whereas cocaine abusers showed an opposite pattern of decreased activity that was reversed by methylphenidate.
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