# Intermittent Fasting Alleviates Anesthesia/Surgery‐Induced Delirium‐Like Behavior in Aged Mice by Remodeling Gut Microbiota

**Authors:** Peiying Huang, Longlu Cao, Tianyu Cao, Xueji Wang, Sichen Cui, Sufang Jiang, Huan Chen, Lichao Di, Sha Li, Lining Huang

PMC · DOI: 10.1002/cns.70748 · 2026-01-22

## TL;DR

Intermittent fasting before surgery helps prevent delirium in old mice by improving gut bacteria and brain mitochondria.

## Contribution

This study shows intermittent fasting prevents delirium via gut microbiota and mitochondrial mechanisms in aged mice.

## Key findings

- Preoperative intermittent fasting reduced delirium-like behaviors in aged mice after surgery.
- IF preserved gut microbiota and short-chain fatty acids, supporting hippocampal mitochondrial health.
- Fecal microbiota transfer and SCFA supplementation replicated IF's protective effects.

## Abstract

Postoperative delirium (POD) is a serious complication in elderly patients, associated with prolonged recovery and adverse outcomes. Recent evidence links POD to mitochondrial dysfunction. While intermittent fasting (IF) has been shown to enhance mitochondrial function and exert neuroprotective effects, potentially through gut microbiota modulation, its ability to prevent POD and the underlying mechanisms remain unclear.

We examined the effects of preoperative IF on delirium‐like behavior in aged mice following anesthesia/surgery. Assessments included neurobehavioral tests, gut microbiota composition, fecal shortchain fatty acids (SCFAs), hippocampal synaptic and mitochondrial ultrastructure via transmission electron microscopy, mitochondrial function, and related molecular markers. To establish causality, fecal microbiota transplantation and SCFA supplementation experiments were conducted.

Preoperative IF significantly attenuated anesthesia/surgery‐induced delirium‐like behaviors. Mechanistically, IF reshaped the gut microbiota and preserved SCFA levels, which collectively maintained hippocampal mitochondrial homeostasis. Both fecal microbiota transplantation and SCFA supplementation replicated the protective effects of IF, confirming the causal role of gut microbiota and its metabolites.

These findings demonstrate that preoperative intermittent fasting mitigates delirium‐like behavior by modulating the gut microbiota–SCFA–mitochondrial axis, highlighting its potential as a non‐pharmacological strategy to enhance neurocognitive resilience and prevent POD in elderly surgical patients.

Preoperative intermittent fasting alleviates postoperative delirium‐like behaviors in aged mice by remodeling gut microbiota and preserving shortchain fatty acids. This gut‐brain interaction maintains hippocampal mitochondrial dynamics and synaptic plasticity, offering a promising non‐pharmacological strategy for perioperative neuroprotection.

## Linked entities

- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, Dlg4 (discs large MAGUK scaffold protein 4) [NCBI Gene 13385] {aka Dlgh4, PSD-95, PSD95, SAP90, SAP90A}, Dnm1l (dynamin 1-like) [NCBI Gene 74006] {aka 6330417M19Rik, Dlp1, Dnmlp1, Drp1, python}, Vdac1 (voltage-dependent anion channel 1) [NCBI Gene 22333] {aka Vdac5, mVDAC1, mVDAC5}, Aktip (AKT interacting protein) [NCBI Gene 14339] {aka AL023020, Fif, Ft, Ft1, Fts}, Ppargc1a (peroxisome proliferative activated receptor, gamma, coactivator 1 alpha) [NCBI Gene 19017] {aka A830037N07Rik, Gm11133, PGC-1, PPARGC-1-alpha, Pgc-1alpha, Pgc1}
- **Diseases:** dysbiosis (MESH:D064806), cognitive impairment (MESH:D003072), Delirium (MESH:D003693), neurological disorders (MESH:D009461), Alzheimer's disease (MESH:D000544), tibial fracture (MESH:D013978), POD (MESH:D000071257), neurocognitive disorders (MESH:D019965), behavioral deficits (MESH:D019958), pain (MESH:D010146), neuroinflammation (MESH:D000090862), Mitochondrial dysfunction (MESH:D028361), neuropathic pain (MESH:D009437), IF (MESH:D007003)
- **Chemicals:** oxygen (MESH:D010100), carbohydrate (MESH:D002241), glycerol (MESH:D005990), helium (MESH:D006371), uranyl acetate (MESH:C005460), acetic acid (MESH:D019342), ATP (MESH:D000255), acetate (MESH:D000085), paraformaldehyde (MESH:C003043), caproic acid (MESH:C037652), MTBE (MESH:C043243), water (MESH:D014867), tetracaine hydrochloride (MESH:D013748), sevoflurane (MESH:D000077149), PBS (MESH:D007854), JC-1 (MESH:C068624), phosphoric acid (MESH:C030242), propionate (MESH:D011422), 4-methylpentanoic acid (MESH:C034527), Alcian blue (MESH:D000423), lidocaine (MESH:D008012), butyrate (MESH:D002087), metronidazole (MESH:D008795), ampicillin (MESH:D000667), neomycin (MESH:D009355), nitrogen (MESH:D009584), glutaraldehyde (MESH:D005976), Short-Chain Fatty Acids (MESH:D005232), vancomycin (MESH:D014640), FITC-dextran (MESH:C015219), AL (-), butyric acid (MESH:D020148)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Enterococcus (genus) [taxon 1350], Lactobacillus (genus) [taxon 1578], Homo sapiens (human, species) [taxon 9606], Bifidobacterium (genus) [taxon 1678], Prevotella (genus) [taxon 838], Alistipes (genus) [taxon 239759]
- **Mutations:** C2003S
- **Cell lines:** H2022206586 — Rattus norvegicus (Rat), Adenocarcinoma of the rat prostate, Cancer cell line (CVCL_Y658), /6 — Homo sapiens (Human), Tongue squamous cell carcinoma, Cancer cell line (CVCL_5985)

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12825212/full.md

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Source: https://tomesphere.com/paper/PMC12825212