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Article Abstract

The ventral striatum (VS) is a key brain region for reward processing and motivation, and its dysfunctions have been implicated in psychiatric disorders such as apathy and obsessive-compulsive disorder. Although functional heterogeneity within the VS has been well established in rodents, its relevance and mechanisms in primates remain unclear. To address this issue, we performed bilateral pharmacological inactivation of the VS in two male macaque monkeys using muscimol, a GABA receptor agonist. Precise targeting was achieved through computed tomography and magnetic resonance imaging. Behavioral effects were evaluated using two methods: a goal-directed task with variable rewards and analysis of spontaneous behavior. Our results demonstrated that anterior (a)VS inactivation induced a hypoactivity state that we termed "resting," whereas posterior (p)VS inactivation elicited compulsive-like "checking" behaviors. Notably, neither the aVS nor the pVS inactivation affected reward value or drive processing, thus differentiating aVS and pVS from those involved in incentive motivation, such as the rostromedial caudate and ventral pallidum. Retrograde tracing demonstrated distinct anatomical projection patterns for the aVS and pVS, supporting their functional segregation. Together, the present results suggest the functional heterogeneity of the primate VS along its anterior-posterior axis, with the aVS and pVS participating in distinct motivational control circuits. Our findings may have important implications for understanding the neural mechanisms of psychiatric disorders and for the development of new therapeutic approaches.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12096147PMC
http://dx.doi.org/10.1523/JNEUROSCI.2430-24.2025DOI Listing

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The ventral striatum (VS) is a key brain region for reward processing and motivation, and its dysfunctions have been implicated in psychiatric disorders such as apathy and obsessive-compulsive disorder. Although functional heterogeneity within the VS has been well established in rodents, its relevance and mechanisms in primates remain unclear. To address this issue, we performed bilateral pharmacological inactivation of the VS in two male macaque monkeys using muscimol, a GABA receptor agonist.

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