Direct serotonin release in humans shapes aversive learning and inhibition

The role of serotonin in human behaviour is informed by approaches which allow in vivo modification of synaptic serotonin. However, characterising the effects of increased serotonin signalling in human models of behaviour is challenging given the limitations of available experimental probes, notably selective serotonin reuptake inhibitors. Here we use a now-accessible approach to directly increase synaptic serotonin in humans (a selective serotonin releasing agent) and examine its influence on domains of behaviour historically considered core functions of serotonin. Computational techniques, including reinforcement learning and drift diffusion modelling, explain participant behaviour at baseline and after week-long intervention. Reinforcement learning models reveal that increasing synaptic serotonin reduces sensitivity for outcomes in aversive contexts. Furthermore, increasing synaptic serotonin enhances behavioural inhibition, and shifts bias towards impulse control during exposure to aversive emotional probes. These effects are seen in the context of overall improvements in memory for neutral verbal information. Our findings highlight the direct effects of increasing synaptic serotonin on human behaviour, underlining its role in guiding decision-making within aversive and more neutral contexts, and offering implications for longstanding theories of central serotonin function.

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Publication Details

Journal
Nature Communications
Published
2024-08-09
DOI
https://doi.org/10.1038/s41467-024-50394-x
Citations
12
Primary Topic
Neurotransmitter Receptor Influence on Behavior
Type
article
Field-Weighted Citation Impact
3.22

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article

Direct serotonin release in humans shapes aversive learning and inhibition

Catherine J. Harmer, Philip J. Cowen, Chloe Wigg, Hosana Tagomori et al.
12 citations
Nature Communications
Neurotransmitter Receptor Influence on Behavior
3.22
article

Direct serotonin release in humans shapes aversive learning and inhibition

Catherine J. Harmer, Philip J. Cowen, Chloe Wigg, Hosana Tagomori, Michael Colwell, Michael Browning, Susannah E. Murphy, Hoi Iao Cheng, Fei Shang
article en
12 citations

Abstract

The role of serotonin in human behaviour is informed by approaches which allow in vivo modification of synaptic serotonin. However, characterising the effects of increased serotonin signalling in human models of behaviour is challenging given the limitations of available experimental probes, notably selective serotonin reuptake inhibitors. Here we use a now-accessible approach to directly increase synaptic serotonin in humans (a selective serotonin releasing agent) and examine its influence on domains of behaviour historically considered core functions of serotonin. Computational techniques, including reinforcement learning and drift diffusion modelling, explain participant behaviour at baseline and after week-long intervention. Reinforcement learning models reveal that increasing synaptic serotonin reduces sensitivity for outcomes in aversive contexts. Furthermore, increasing synaptic serotonin enhances behavioural inhibition, and shifts bias towards impulse control during exposure to aversive emotional probes. These effects are seen in the context of overall improvements in memory for neutral verbal information. Our findings highlight the direct effects of increasing synaptic serotonin on human behaviour, underlining its role in guiding decision-making within aversive and more neutral contexts, and offering implications for longstanding theories of central serotonin function.

Nature CommunicationsVol. 15(1)
Oxford Health NHS Foundation Trust (GB), Warneford Hospital (GB), University of Oxford (GB)
Zogenix, National Institute for Health and Care Research, UCB Pharma
Peace, Justice and strong institutions
Openalex Percentile: Top 8%
Neurotransmitter Receptor Influence on Behavior
3.22
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