# A Common Neuronal Ensemble in the Lateral Habenula Regulates Ciprofol Anesthesia in Mice

**Authors:** Kang Zhou, Lin-Chen Zhang, He Zhu, Bei Wen, Jia-Li Tang, Ping-Chuan Yuan, A-Fang Zhu, Yu-Guang Huang

PMC · DOI: 10.3390/ph17030363 · Pharmaceuticals · 2024-03-11

## TL;DR

This study identifies a specific group of neurons in mice that control the effects of a new anesthetic drug called ciprofol.

## Contribution

The study reveals a specific role of lateral habenula neurons in regulating ciprofol anesthesia, which was previously unexplored.

## Key findings

- Ciprofol induces c-Fos expression in the lateral habenula of mice.
- Ablation of these neurons speeds up recovery from ciprofol anesthesia.
- Activating these neurons deepens the hypnotic state during anesthesia.

## Abstract

General anesthetics were first used over 170 years ago; however, the mechanisms of how general anesthetics induce loss of consciousness (LOC) remain unclear. Ciprofol, a novel intravenous anesthetic, has been developed by incorporating cyclopropyl into the chemical structure of propofol. This modification offers the benefits of rapid onset and minimal injection pain. Recent studies have revealed that the glutamatergic neurons of the lateral habenula (LHb) play a crucial role in modulating the LOC induced by propofol and sevoflurane. Nevertheless, the specific involvement of LHb in the anesthetic effects of ciprofol remains uncertain. Here, using targeted recombination in active populations (TRAP) combined with electroencephalogram/electromyography recordings and the righting reflex behavioral test, our study revealed that intravenous infusion of ciprofol for 1 h could lead to the induction of c-Fos expression in the LHb in mice. The combination of TRAP and gene ablation, aimed at selectively ablating ciprofol-activated neurons in the LHb, has been shown to facilitate the emergence of ciprofol anesthesia and decrease the proportion of delta waves during the emergence phase. Chemogenetic inhibition of these neurons produced a comparable effect, whereas chemogenetic activation resulted in the opposite outcome. Chemogenetic activation of ciprofol-activated neurons in the LHb delays the emergence of anesthesia and induces a deep hypnotic state during the emergence phase. Taken together, our findings suggest that LHb ciprofol-activated neurons modulate the state of consciousness and could potentially be targeted to manipulate consciousness during ciprofol anesthesia.

## Linked entities

- **Genes:** FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353]
- **Chemicals:** ciprofol (PubChem CID 86301664), propofol (PubChem CID 4943), sevoflurane (PubChem CID 5206), cyclopropyl (PubChem CID 123162)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353] {aka AP-1, C-FOS, p55}
- **Diseases:** pain (MESH:D010146), LOC (MESH:D014474)
- **Chemicals:** sevoflurane (MESH:D000077149), propofol (MESH:D015742), Ciprofol (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10975929/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC10975929/full.md

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Source: https://tomesphere.com/paper/PMC10975929