# Subclinical infection combined with surgery induced cognitive dysfunction: a novel adult mouse model for perioperative neurocognitive disorder

**Authors:** Chenchen Xia, Xiao Zhang, Wanbing Dai, Yizhe Zhang, Ye Liu, Xiangyang Cheng, Yeke Zhu, Lili Huang, Minghao Tang, Yongxing Yao, Xuwu Xiang, Weifeng Yu, Diansan Su

PMC · DOI: 10.3389/fnagi.2025.1691681 · Frontiers in Aging Neuroscience · 2026-01-12

## TL;DR

This study introduces a new mouse model for perioperative neurocognitive disorder by combining subclinical infection with surgery, causing cognitive impairments.

## Contribution

A novel adult mouse model for PND using preoperative subclinical infection and surgery is developed.

## Key findings

- Preoperative LPS increased neuroinflammation and microglial activation after surgery.
- Cognitive impairments in memory and learning were observed in mice.
- Synaptic proteins like PSD-95 and BDNF were reduced, indicating disrupted synaptic function.

## Abstract

Perioperative neurocognitive disorder (PND) describes a range of cognitive impairments associated with surgery and anaesthesia, often driven by neuroinflammation. This study explored a novel adult mouse model, in which preoperative subclinical infection, induced by low-dose lipopolysaccharide (LPS) in combination with surgery, led to cognitive dysfunction in adult mice.

Adult male C57BL/6J mice were treated with 0.75 mg/kg LPS two hours before undergoing tibial fracture fixation or appendicectomy. Spontaneous activity and anxiety-like behaviours were tested by open field test. Cognitive outcomes were evaluated using the novel object recognition test and morris water maze. Inflammatory markers and synaptic proteins in the hippocampus were analysed through ELISA, RT-qPCR, and Western blot, while proteomics provided deeper insights into molecular changes.

We found that preoperative LPS sensitised the immune system, leading to heightened neuroinflammation and microglial activation after surgery. This was accompanied by memory and learning impairments. Key synaptic proteins, including PSD-95, GAP-43, SYN and mature BDNF, were significantly reduced, indicating disrupted synaptic function. Proteomics revealed changes in pathways related to immune responses, synaptic organisation, and energy metabolism, providing a potential molecular basis for these cognitive deficits.

This study provided a practical adult mouse model for PND, demonstrating that low-dose LPS followed by surgery induced an inflammatory response, leading to postoperative impairments in learning and memory.

## Linked entities

- **Proteins:** DLG4 (discs large MAGUK scaffold protein 4), GAP43 (growth associated protein 43), FYN (FYN proto-oncogene, Src family tyrosine kinase), BDNF (brain derived neurotrophic factor)

## Full-text entities

- **Genes:** Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], jt (joined toes) [NCBI Gene 16473] {aka syn}, Dlg4 (discs large MAGUK scaffold protein 4) [NCBI Gene 13385] {aka Dlgh4, PSD-95, PSD95, SAP90, SAP90A}, Gap43 (growth associated protein 43) [NCBI Gene 14432] {aka B-50, Basp2, GAP-43}
- **Diseases:** neuroinflammation (MESH:D000090862), infection (MESH:D007239), cognitive deficits (MESH:D003072), tibial fracture (MESH:D013978), Inflammatory (MESH:D007249), anxiety (MESH:D001007), PND (MESH:D019965), impairments in learning and memory (MESH:D007859)
- **Chemicals:** LPS (MESH:D008070)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12832885/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12832885/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12832885/full.md

---
Source: https://tomesphere.com/paper/PMC12832885