# A dopaminergic projection from the ventral tegmental area to the dorsal raphe nucleus critically regulates propofol anesthesia in mice

**Authors:** Junjie He, Tianxi Yao, Huan Guo, Haichuan He, Zhuangzhuang Tian, Ketao Ma, Jiangwen Yin, Yan Li

PMC · DOI: 10.1186/s13062-026-00736-0 · Biology Direct · 2026-02-09

## TL;DR

This study identifies a brain circuit connecting the VTA and DRN that controls propofol anesthesia in mice, offering new insights into how consciousness is regulated during anesthesia.

## Contribution

The study reveals a novel VTADA→DRN5-HT circuit that bidirectionally regulates propofol anesthesia in mice.

## Key findings

- VTADA terminals and DRN5-HT neurons are anatomically connected and functionally linked.
- Activation of VTADA or DRN5-HT neurons shortens propofol anesthesia, while inhibition prolongs it.
- Optogenetic activation of VTADA terminals rapidly induces arousal from propofol anesthesia.

## Abstract

General anesthesia induces a reversible loss of consciousness, yet the precise neural circuits mediating this state transition remain incompletely understood. The ventral tegmental area (VTA) dopaminergic (DA) neurons and the dorsal raphe nucleus (DRN) serotonergic (5-HT) neurons are key components of the ascending arousal system. This study investigated the existence and functional role of VTADA→DRN5-HT circuit in regulating propofol anesthesia. Using virus-mediated neural circuit tracing in DAT-Cre and TPH2-CreER transgenic mice, we demonstrated an anatomically connected circuit appositions between VTADA axon terminals and DRN5-HT neurons. In vivo fiber photometry revealed that the activity of both presynaptic VTADA terminals in the DRN and postsynaptic DRN5-HT neurons was significantly suppressed under propofol anesthesia. Chemogenetic activation of either VTADA or DRN5-HT neurons facilitated emergence from propofol anesthesia, whereas their inhibition prolonged the duration of anesthesia. Optogenetic activation of VTADA terminals within the DRN rapidly induced behavioral and electroencephalographic (EEG) arousal from stable propofol anesthesia. Crucially, this pro-arousal effect was abolished by chemogenetic inhibition of DRN5-HT neurons, indicating a functional hierarchy. These findings identify a putative direct pathway VTADA→DRN5-HT circuit that bidirectionally regulates propofol anesthesia, providing a novel neural substrate for conscious state control and a potential target for therapeutic interventions.

The online version contains supplementary material available at 10.1186/s13062-026-00736-0.

## Linked entities

- **Chemicals:** propofol (PubChem CID 4943)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Chemicals:** propofol (MESH:D015742)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12969853/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12969853/full.md

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Source: https://tomesphere.com/paper/PMC12969853