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Primate Nigrostriatal Dopamine System Regulates Saccadic Response Inhibition
- Source :
- Neuron. 100:1513-1526.e4
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- Animals need to inhibit inappropriate actions that would lead to unwanted outcomes. Although this ability, called response inhibition, is impaired in neurological/psychiatric disorders with dopaminergic dysfunctions, how dopamine regulates response inhibition remains unclear. Here we investigated neuronal signals of the nigrostriatal dopamine system in monkeys performing a saccadic countermanding task. Subsets of dopamine neurons in the substantia nigra and striatal neurons receiving the dopaminergic input were activated when the monkey was required to cancel a planned saccadic eye movement. These activations were stronger when canceling the eye movements was successful compared with failed and were enhanced in demanding trials. The activated dopamine neurons were distributed mainly in the dorsolateral, but not in the ventromedial, part of the nigra. Furthermore, pharmacological blockade of dopaminergic neurotransmission in the striatum dampened the performance of canceling saccadic eye movements. The present findings indicate that disruption of nigrostriatal dopamine signaling causes impairments in response inhibition.
- Subjects :
- Male
0301 basic medicine
Signal Detection, Psychological
Caudate nucleus
Action Potentials
Substantia nigra
Striatum
Functional Laterality
03 medical and health sciences
0302 clinical medicine
Dopamine
Basal ganglia
Reaction Time
Saccades
medicine
Animals
business.industry
Dopaminergic Neurons
General Neuroscience
Dopaminergic
Eye movement
Neural Inhibition
Benzazepines
Macaca mulatta
Corpus Striatum
Saccadic masking
Substantia Nigra
030104 developmental biology
ROC Curve
nervous system
Dopamine Antagonists
Haloperidol
business
Neuroscience
030217 neurology & neurosurgery
medicine.drug
Subjects
Details
- ISSN :
- 08966273
- Volume :
- 100
- Database :
- OpenAIRE
- Journal :
- Neuron
- Accession number :
- edsair.doi.dedup.....df31330e2c0079da41bbc2fd3fa49bbc
- Full Text :
- https://doi.org/10.1016/j.neuron.2018.10.025