Stimulus-dependent dopamine dynamics from locus coeruleus axons

Arousal is essential for survival, and maladaptive arousal processing leads to an inability to focus, anxiety-like behavior, and dysregulated affective states. Norepinephrine (NE) is known to regulate anxiety, arousal, and learning through locus coeruleus (LC) projections throughout the brain. Evidence for co-release of the NE precursor and neurotransmitter dopamine (DA) from LC neurons has been accumulating for years, yet definitive measures of DA release across regions, stimulus paradigms, and behaviors associated with the LC-NE system remain controversial. Here, we identified the physiological and behavioral properties that evoke DA release from LC axon terminals. Using concomitant approaches, we inhibited the LC and ventral tegmental area (VTA) to selectively isolate the contributions of LC-derived DA release. Together these findings establish the constraints by which LC neurons release DA in a modality-dependent manner.

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Publication Details

Journal
Cell Reports
Published
2026-07-25
DOI
https://doi.org/10.1016/j.celrep.2026.117729
Citations
1
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
4.69

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article

Stimulus-dependent dopamine dynamics from locus coeruleus axons

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Neuroscience and Neuropharmacology Research
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article

Stimulus-dependent dopamine dynamics from locus coeruleus axons

Elena Seaholm, Sean C. Piantadosi, Avi K. Matarasso, David Weinshenker, Li Li, Yulong Li, Michael R. Bruchas, Itzel Rodriguez Reyes, Ashritha Cheeyandira
article en
1 citations

Abstract

Arousal is essential for survival, and maladaptive arousal processing leads to an inability to focus, anxiety-like behavior, and dysregulated affective states. Norepinephrine (NE) is known to regulate anxiety, arousal, and learning through locus coeruleus (LC) projections throughout the brain. Evidence for co-release of the NE precursor and neurotransmitter dopamine (DA) from LC neurons has been accumulating for years, yet definitive measures of DA release across regions, stimulus paradigms, and behaviors associated with the LC-NE system remain controversial. Here, we identified the physiological and behavioral properties that evoke DA release from LC axon terminals. Using concomitant approaches, we inhibited the LC and ventral tegmental area (VTA) to selectively isolate the contributions of LC-derived DA release. Together these findings establish the constraints by which LC neurons release DA in a modality-dependent manner.

Cell ReportsVol. 45(8)
Center for Infectious Disease Research (US), Emory University (US), University of Washington (US), Peking University (CN), Norcliffe Foundation (US), Rice University (US)
University of Washington, National Institute of Mental Health, National Institute on Drug Abuse
Openalex Percentile: Top 13%
Neuroscience and Neuropharmacology Research
4.69
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