4.7 Article

Dopamine Axons in Dorsal Striatum Encode Contralateral Visual Stimuli and Choices

Journal

JOURNAL OF NEUROSCIENCE
Volume 41, Issue 34, Pages 7197-7205

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0490-21.2021

Keywords

dopamine; dorsal striatum; mice; sensory uncertainty; ventral striatum; visual decision

Categories

Funding

  1. Wellcome Trust [213465, 205093]
  2. GlaxoSmithKline/Fight for Sight Chair in Visual Neuroscience

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Research suggests that dopamine in the striatum plays a critical role in visual decision-making, encoding visual stimuli and rewarded actions in a lateralized fashion. Contrary to previous beliefs, dopamine signals in the DMS respond to contralateral stimuli and rewarded actions, facilitating associations between specific visual stimuli and actions.
The striatum plays critical roles in visually-guided decision-making and receives dense axonal projections from midbrain dopamine neurons. However, the roles of striatal dopamine in visual decision-making are poorly understood. We trained male and female mice to perform a visual decision task with asymmetric reward payoff, and we recorded the activity of dopamine axons innervating striatum. Dopamine axons in the dorsomedial striatum (DMS) responded to contralateral visual stimuli and contralateral rewarded actions. Neural responses to contralateral stimuli could not be explained by orienting behavior such as eye movements. Moreover, these contralateral stimulus responses persisted in sessions where the animals were instructed to not move to obtain reward, further indicating that these signals are stimulus-related. Lastly, we show that DMS dopamine signals were qualitatively different from dopamine signals in the ventral striatum (VS), which responded to both ipsilateral and contralateral stimuli, conforming to canonical prediction error signaling under sensory uncertainty. Thus, during visual decisions, DMS dopamine encodes visual stimuli and rewarded actions in a lateralized fashion, and could facilitate associations between specific visual stimuli and actions.

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