# Zolpidem restores sleep and decreases amyloid in a mouse model

**Authors:** Lu Yu, Shinya Yokomizo, Tri H. Doan, Qiuchen Zhao, Akshatha Ganne, Meenakshisundaram Balasubramaniam, Ksenia V. Kastanenka

PMC · DOI: 10.1002/alz.71175 · 2026-03-11

## TL;DR

Zolpidem improves sleep and reduces amyloid in a mouse model of Alzheimer's disease, suggesting potential early-stage therapeutic benefits.

## Contribution

Zolpidem is shown to restore sleep rhythms and reduce amyloid plaque burden in a mouse model of Alzheimer's disease.

## Key findings

- Zolpidem restored NREM sleep and rescued slow oscillation brain rhythms in APP/PS1 mice.
- Zolpidem reduced cortical amyloid plaque burden and neuronal calcium overload.
- Zolpidem improved sleep-dependent memory consolidation without affecting locomotion.

## Abstract

Deficits in non–rapid eye movement (NREM) sleep facilitate Alzheimer's disease (AD) progression. Enhancing gamma‐aminobutyric acid‐ergic (GABAergic) signaling can restore sleep. Unbiased computational analysis identified zolpidem as high‐affinity GABA receptor modulator facilitating chloride transport that could slow AD.

Zolpidem's effects on sleep and Alzheimer's progression were evaluated in young APP/PS1 (amyloid precursor protein/presenilin 1) mice. Sleep was monitored with electroencephalography/electromyography (EEG/EMG) telemetry. Wide‐field imaging with voltage‐sensitive dyes (VSDs) was used to track sleep‐dependent brain rhythms. Multiphoton microscopy allowed assessments of amyloid plaque load and basal neuronal calcium levels. Behavioral assays were used to measure memory and cognitive function.

Zolpidem restored NREM sleep and rescued sleep‐dependent brain rhythm, slow oscillation. Zolpidem administration reduced cortical amyloid plaque burden, mitigated neuronal calcium overload, and enhanced sleep‐dependent contextual recall without adverse effects on locomotion.

Zolpidem effectively decreased amyloid in young APP/PS1 mice. This supports zolpidem's therapeutic promise as an intervention strategy at early stages of AD.

Zolpidem treatment improves non–rapid eye movement (NREM) sleep stability and reduces sleep fragmentation.Zolpidem restores slow oscillation in young APP/PS1 (amyloid precursor protein/presenilin 1) mice.Zolpidem treatment reduces amyloid plaque burden and calcium overload in neurons.Zolpidem‐treated mice show improved sleep‐dependent memory consolidation.Sleep rhythm enhancement shows promise for Alzheimer's therapy.

Zolpidem treatment improves non–rapid eye movement (NREM) sleep stability and reduces sleep fragmentation.

Zolpidem restores slow oscillation in young APP/PS1 (amyloid precursor protein/presenilin 1) mice.

Zolpidem treatment reduces amyloid plaque burden and calcium overload in neurons.

Zolpidem‐treated mice show improved sleep‐dependent memory consolidation.

Sleep rhythm enhancement shows promise for Alzheimer's therapy.

## Linked entities

- **Chemicals:** zolpidem (PubChem CID 5732)
- **Diseases:** Alzheimer's disease (MONDO:0004975)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cfp (complement factor properdin) [NCBI Gene 18636] {aka BCFG, Pfc}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, Psen1 (presenilin 1) [NCBI Gene 19164] {aka Ad3h, PS-1, PS1, S182}, Slc32a1 (solute carrier family 32 (GABA vesicular transporter), member 1) [NCBI Gene 22348] {aka VGAT, Viaat}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}, Bsn (bassoon) [NCBI Gene 12217], Gabrg1 (gamma-aminobutyric acid type A receptor subunit gamma 1) [NCBI Gene 14405] {aka GabaA, GabaA/BZ}, Gphn (gephyrin) [NCBI Gene 268566] {aka 5730552E08Rik, C230040D23, GPH, GPHRYN, geph}
- **Diseases:** anxiety (MESH:D001007), neuroinflammation (MESH:D000090862), traumatic brain injury (MESH:D000070642), brain atrophy (MESH:C566985), AD (MESH:D000544), neurotoxicity (MESH:D020258), Parkinson's disease (MESH:D010300), Sleep (MESH:D012893), calcium overload (MESH:D019190), RESEARCH (MESH:D014947), neurodegenerative disorder (MESH:D019636), shock (MESH:D012769), synaptic toxicity (MESH:D012183), Deficits (MESH:D009461), stroke (MESH:D020521), Slow oscillation (MESH:D012897), falls (MESH:C537863), toxicity (MESH:D064420), VSD (MESH:D003807), NREM sleep deficits (MESH:D020187), memory impairment (MESH:D008569), cognitive decline (MESH:D003072), amyloid plaques (MESH:D058225), synaptic dysfunction (MESH:C536122), amyloid (MESH:C000718787), dementia (MESH:D003704), cortical hyperexcitability (MESH:D054220), calcium (MESH:D002128), sleep deprivation (MESH:D012892), neuronal loss (MESH:D009410), amyloidosis (MESH:D000686)
- **Chemicals:** flumazenil (MESH:D005442), POPC (MESH:C065191), oxygen (MESH:D010100), NaCl (MESH:D012965), chloride (MESH:D002712), ethanol (MESH:D000431), Lemborexant (MESH:C000634104), GABA (MESH:D005680), isoflurane (MESH:D007530), Diazepam (MESH:D003975), water (MESH:D014867), Zolpidem (MESH:D000077334), Cl- (MESH:D002713), Ti (MESH:D014025), NTG (MESH:D005996), BZD (MESH:D001569), ML (-), eszopiclone (MESH:D000069582), Calcium (MESH:D002118), DMSO (MESH:D004121), lipid (MESH:D008055), Methoxy-X04 (MESH:C465418)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** histidine in position 105

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12976976/full.md

---
Source: https://tomesphere.com/paper/PMC12976976