Social reward outcompetes drug seeking dopaminergic ensembles to prevent relapse

Drugs of abuse promote substance use disorder (SUD) by hijacking mesolimbic circuits that normally process natural rewards. Among these, social rewards exhibit therapeutic potential, but the underlying neural substrates remain unclear. Using a multimodal approach integrating in vivo single-neuron calcium imaging, optogenetic manipulation, and electrophysiology in male rats, we identified two distinct dopaminergic ensembles in the ventral tegmental area (VTA) that respectively encode social reward and drug seeking. Notably, these antagonistic ensembles exert reciprocal influence through competitive interactions that shape behavioral outcomes. Furthermore, circuit mapping revealed divergent connectivity patterns, with social reward-responsive dopaminergic ensembles receiving preferential input from the dorsal raphe nucleus (DRN). Activation of the DRN-VTA pathway recapitulates the protective effects of social reward against drug seeking. In this study, we uncovered a dynamic competition between functionally specialized dopaminergic ensembles through which social reward attenuates drug seeking, offering insights that may inform development of novel strategies for SUD treatment.

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Publication Details

Journal
Nature Communications
Published
2026-04-03
DOI
https://doi.org/10.1038/s41467-026-71357-4
Primary Topic
Neurotransmitter Receptor Influence on Behavior
Type
article
Field-Weighted Citation Impact
0.00

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article

Social reward outcompetes drug seeking dopaminergic ensembles to prevent relapse

Tangsheng Lu, Xuefang Guan, Jeffrey W. Grimm, Zhe Wang et al.
Nature Communications
Neurotransmitter Receptor Influence on Behavior
article

Social reward outcompetes drug seeking dopaminergic ensembles to prevent relapse

Tangsheng Lu, Xuefang Guan, Jeffrey W. Grimm, Zhe Wang, Xinyou Lv, J. Shi, Xiaoxing Liu, Kai Yuan, Wei Zheng, Trevor W. Robbins, Xue Li, Yan-Xue Xue
article en

Abstract

Drugs of abuse promote substance use disorder (SUD) by hijacking mesolimbic circuits that normally process natural rewards. Among these, social rewards exhibit therapeutic potential, but the underlying neural substrates remain unclear. Using a multimodal approach integrating in vivo single-neuron calcium imaging, optogenetic manipulation, and electrophysiology in male rats, we identified two distinct dopaminergic ensembles in the ventral tegmental area (VTA) that respectively encode social reward and drug seeking. Notably, these antagonistic ensembles exert reciprocal influence through competitive interactions that shape behavioral outcomes. Furthermore, circuit mapping revealed divergent connectivity patterns, with social reward-responsive dopaminergic ensembles receiving preferential input from the dorsal raphe nucleus (DRN). Activation of the DRN-VTA pathway recapitulates the protective effects of social reward against drug seeking. In this study, we uncovered a dynamic competition between functionally specialized dopaminergic ensembles through which social reward attenuates drug seeking, offering insights that may inform development of novel strategies for SUD treatment.

Nature CommunicationsVol. 17(1)
University of Science and Technology of China (CN), Henan University (CN), Peking University (CN), University of Cambridge (GB), Chinese Institute for Brain Research (CN), National Institutes for Food and Drug Control (CN), Center for Life Sciences (CN), Peking University Sixth Hospital (CN), Shandong First Medical University (CN), Shanghai Center for Brain Science and Brain-Inspired Technology (CN), Western Washington University (US)
National Natural Science Foundation of China
Good health and well-being
Openalex Percentile: Top 32%
Neurotransmitter Receptor Influence on Behavior
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