# Paraventricular nucleus–locus coeruleus VGlut2 neural circuit regulates energy metabolism in mice

**Authors:** Haodong Liu, Penghui Li, Mingyang Yu, Xin Zhang, Hefeng Zhu, Yang He, Zelin Zhang, Xiaolong Li, Bingkun Teng, Jiaxin Fan, Wenchao Yang, Junzhe Yin, Qinqin Hao, Guifang Cao, Haijun Li, Shuying Liu, Yongqiang Li, Junguang Ren, Yujie Chen, Chenguang Du

PMC · DOI: 10.1038/s41419-025-08238-z · Cell Death & Disease · 2025-12-09

## TL;DR

A brain circuit involving PVHVGlut2 neurons and the locus coeruleus helps regulate energy metabolism and combat obesity in mice.

## Contribution

Identifies a novel neural circuit linking PVHVGlut2 neurons to the locus coeruleus in regulating energy metabolism and obesity.

## Key findings

- PVHVGlut2 neurons are activated during high-fat diets and inhibit feeding while enhancing brown fat thermogenesis.
- Optogenetic activation of the PVHVGlut2→LC circuit reduces food intake and increases brown fat temperature.
- Long-term activation of this circuit ameliorates obesity and insulin resistance in mice.

## Abstract

The role of the central nervous system in energy homoeostasis remains unclear. This study examined the role of VGlut2-expressing neurons in the paraventricular nucleus of the hypothalamus (PVHVGlut2) and their downstream circuits in the regulation of energy homoeostasis. Long-term high-fat diet (HFD) disrupts energy balance and compensatorily activates PVHVGlut2 neurons that innervate interscapular brown adipose tissue (iBAT). These neurons are inhibited during food consumption, suggesting their involvement in feeding and energy metabolism regulation. Activation of PVHVGlut2 neurons reduces food intake and enhances iBAT thermogenesis. Further, optogenetic PVHVGlut2→ locus coeruleus (LC) circuit activation inhibited feeding and elevated iBAT temperature, which was blocked by sympathetic nerve denervation. Long-term chemogenetic PVHVGlut2 → LC neural circuit activation ameliorates HFD-induced obesity and insulin resistance. The PVHVGlut2 → LC circuit integrates feeding inhibition and peripheral thermogenesis signals to regulate energy metabolism, offering potential intervention targets for obesity and other energy homoeostasis disorders.

## Linked entities

- **Genes:** SLC17A6 (solute carrier family 17 member 6) [NCBI Gene 57084]
- **Chemicals:** doxorubicin (PubChem CID 31703)
- **Diseases:** obesity (MONDO:0011122)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Slc17a6 (solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6) [NCBI Gene 140919] {aka 2900073D12Rik, DNPI, VGLUT2}
- **Diseases:** homoeostasis disorders (MESH:D009358), insulin resistance (MESH:D007333), obesity (MESH:D009765)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12830986/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12830986/full.md

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Source: https://tomesphere.com/paper/PMC12830986