Dopamine and acetylcholine correlations in the nucleus accumbens depend on behavioral task states.

IF 8.1 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Current Biology Pub Date : 2025-03-24 Epub Date: 2025-03-03 DOI:10.1016/j.cub.2025.01.064
Kauê Machado Costa, Zhewei Zhang, Douglas Deutsch, Yizhou Zhuo, Guochuan Li, Yulong Li, Geoffrey Schoenbaum
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引用次数: 0

Abstract

Dopamine release in the nucleus accumbens (NAcc) changes quickly in response to errors in predicting events like reward delivery1,2,3 but also slowly ramps up when animals are moving toward a goal.4,5,6,7,8,9,10 This ramping has attracted much recent attention, as there is controversy regarding its computational role5,7,9,11 and whether they are driven by dopamine neuron firing7,8,9 or local circuit mechanisms.5,6 If the latter is true, cholinergic transmission would be a prime candidate mechanism,12,13,14 and acetylcholine and dopamine signals should be positively correlated during behavior, particularly during motivated approach. However, in the dorsal striatum, striatal cholinergic interneurons typically "dip" their activity when reward or associated cues are presented, in opposition to dopamine,15,16,17,18 and acetylcholine and dopamine release is generally anti-correlated in vivo.19,20 Furthermore, acetylcholine and dopamine have opposing effects on downstream striatal projection neurons (SPNs),21,22 which suggests that cholinergic dips create a permissive window for dopamine to drive plasticity.23 These studies therefore suggest that dopamine and acetylcholine should be anti-correlated during behavior. We tested between these hypotheses by simultaneously recording accumbal dopamine and acetylcholine signals in rats executing a task involving motivated approach. We found that dopamine ramps were not coincidental with changes in acetylcholine. Instead, acetylcholine was positively, negatively, or uncorrelated with dopamine depending on the task phase. Our results suggest that accumbal dopamine and acetylcholine dynamics are largely independent but may combine to engage different postsynaptic mechanisms depending on task demands.

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来源期刊
Current Biology
Current Biology 生物-生化与分子生物学
CiteScore
11.80
自引率
2.20%
发文量
869
审稿时长
46 days
期刊介绍: Current Biology is a comprehensive journal that showcases original research in various disciplines of biology. It provides a platform for scientists to disseminate their groundbreaking findings and promotes interdisciplinary communication. The journal publishes articles of general interest, encompassing diverse fields of biology. Moreover, it offers accessible editorial pieces that are specifically designed to enlighten non-specialist readers.
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