ArticlebioRxiv : the preprint server for biology2026
Coordinated yet asymmetric striatal neuromodulatory dynamics encode associative learning.
Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
The striatum integrates dopamine and acetylcholine to support learning and behavioral flexibility, yet how these neuromodulators coordinate during associative learning remains unclear. Using longitudinal dual-color fiber photometry in mice, we simultaneously tracked both signals in the anterior dorsolateral striatum throughout Pavlovian conditioning. We find that learning recruits distinct forms of neuromodulatory plasticity: dopamine maintains rapid, contingency-dependent cue responses, whereas acetylcholine undergoes broader reorganization across training. Despite these differences, trial-by-trial covariance between the two signals converges onto a compact low-dimensional structure that reliably captures learned behavioral state and distinguishes associative learning from sensory exposure alone. Granger causality analyses further reveal a directional asymmetry, present in both paired and unpaired mice, whereby dopamine reliably predicts subsequent acetylcholine fluctuations, with only weak reciprocal prediction. Together, our results identify a low-dimensional organizational principle for dopamine-acetylcholine interactions, and suggest that dopamine acts as a leading temporal signal that shapes cholinergic dynamics during striatal learning.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.