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The effects of pramipexole on motivational vigour during a saccade task: a placebo-controlled study in healthy adults

Abstract:
Motivation allows us to energise actions when we expect reward and is reduced in depression. This effect, termed motivational vigour, has been proposed to rely on central dopamine, with dopaminergic agents showing promise in the treatment of depression. This suggests that dopaminergic agents might act to reduce depression by increasing the effects of reward or by helping energise actions. The aim of the current study was to investigate whether the dopamine agonist pramipexole enhanced motivational vigour during a rewarded saccade task. In addition, we asked whether the effects of pramipexole on vigour differ between reward contingent on performance and guaranteed reward. Healthy adult participants were randomised to receive either pramipexole (n = 19) or placebo (controls n = 18) for 18 days. The vigour of saccades was measured twice, once before the administration of study medication (Time 1) and after taking it for 12-15 days (Time 2). To separate motivation by contingency vs. reward, saccadic vigour was separately measured when (1) rewards were contingent on performance (2) delivered randomly with matched frequency, (3) when reward was guaranteed, (4) when reward was not present at all. Motivation increased response vigour, as expected. Relative to placebo, pramipexole also increased response vigour. However, there was no interaction, meaning that the effects of reward were not modulated by drug, and there was no differential drug effect on contingent vs. guaranteed rewards. The effect of pramipexole on vigour could not be explained by a speed/accuracy trade-off, nor by autonomic arousal as indexed by pupillary dilation. Chronic D2 stimulation increases general vigour, energising movements in healthy adults irrespective of extrinsic reward.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1007/s00213-024-06567-z

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Psychiatry
Role:
Author
ORCID:
0000-0002-0516-4755
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Psychiatry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Psychiatry
Role:
Author
ORCID:
0000-0001-9632-0823
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Psychiatry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Psychiatry
Oxford college:
St Cross College
Role:
Author
ORCID:
0000-0001-9108-3144


More from this funder
Grant:
National Institute for Health and Care Research


Publisher:
Springer Nature
Journal:
Psychopharmacology More from this journal
Volume:
241
Issue:
7
Pages:
1365–1375
Place of publication:
Germany
Publication date:
2024-03-18
Acceptance date:
2024-02-28
DOI:
EISSN:
1432-2072
ISSN:
0033-3158
Pmid:
38494550


Language:
English
Keywords:
Pubs id:
1885335
Local pid:
pubs:1885335
Deposit date:
2024-06-25

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