ArticleCommunications biology2025
Higher dopamine D1 receptor expression in prefrontal parvalbumin neurons underlies higher distractibility in marmosets versus macaques.
Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Dopamine D1 and D2 receptors differentially control strength and dynamics of abstract decision codes in the primate prefrontal cortex.Proceedings of the National Academy of Sciences of the United States of America · 2026Article
- From comparative connectomics to large-scale working memory modeling in macaque and marmoset.Cell reports · 2026Article
- From comparative connectomics to large-scale working memory modeling in macaque and marmoset.bioRxiv : the preprint server for biology · 2025Article
- Higher dopamine D1 receptor expression in prefrontal parvalbumin neurons underlies higher distractibility in marmosets versus macaques.Communications biology · 2025Article
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Authors and funding
18 authors.
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Abstract
Marmosets and macaques are common nonhuman primate models of cognition, yet marmosets appear more distractible and perform worse in cognitive tasks. The dorsolateral prefrontal cortex (dlPFC) is pivotal for sustained attention, and research in macaques suggests that dopaminergic modulation and inhibitory parvalbumin (PV) neurons could influence distractor resistance. Here we compare the two species using a visual fixation task with distractors, perform molecular and anatomical analyses in dlPFC, and link functional microcircuitry with cognitive performance using computational modeling. We show that marmosets are more distractible than macaques, and that marmoset dlPFC PV neurons contain higher levels of dopamine D1 receptor (D1R) transcripts and protein, similar to levels in mice. Our modeling indicates that higher D1R expression in marmoset dlPFC PV neurons may increase distractibility by making dlPFC microcircuits more vulnerable to disruptions of their task-related persistent activity, especially when dopamine is released in dlPFC in response to unexpected salient stimuli.
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