# Effects of Eisenia bicyclis Extract on Sleep Promotion in a Caffeine-Induced Insomnia Models

**Authors:** Yeon Ji Ha, Sekyung Lee, Hyung Joo Suh, Yejin Ahn, Hyunjae Kim, Yu-Kyong Shin, Ki-Bae Hong

PMC · DOI: 10.4014/jmb.2509.09008 · Journal of Microbiology and Biotechnology · 2025-10-27

## TL;DR

This study shows that Eisenia bicyclis extract helps reduce insomnia caused by caffeine in fruit flies and mice by improving sleep quality and reducing brain damage.

## Contribution

The study demonstrates the novel sleep-promoting effects of Eisenia bicyclis extract in caffeine-induced insomnia models.

## Key findings

- EB treatment normalized disrupted sleep patterns and reduced sleep fragmentation in caffeine-exposed fruit flies.
- EB reduced caffeine-induced hyperactivity and brain damage by enhancing antioxidant defenses and neurotransmitter levels.
- EB restored caffeine-reduced sleep duration in mice without affecting sleep latency.

## Abstract

This study investigated the sleep-promoting effects of the brown alga Eisenia bicyclis (EB), which contains phlorotannins, using caffeine-induced insomnia models of Drosophila melanogaster and ICR mice. In flies exposed to caffeine, EB treatment dose-dependently normalized disrupted nighttime activity and total sleep duration, while high-dose EB significantly reduced sleep fragmentation by decreasing the number of sleep bouts. Locomotor tracking analysis further showed that EB attenuated caffeine-induced hyperactivity, reducing distance moved, velocity, and mobility to levels comparable with the normal and benzodiazepine (BDZ)-treated groups. In the pentobarbital-induced sleep test with mice, EB restored the caffeine-induced reduction in sleep duration, although sleep latency remained unaffected. Moreover, EB significantly reduced elevated brain malondialdehyde levels induced by caffeine, accompanied by increased expression of antioxidant-related enzymes. Neurochemical analyses revealed that EB enhanced the levels of γ-aminobutyric acid (GABA) and serotonin, as well as the expression of their receptors, effectively reversing caffeine-induced reductions. These findings suggest that EB exerts sleep-promoting effects by modulating behavioral activity, enhancing antioxidant defense, and regulating GABAergic and serotonergic neurotransmission. Collectively, our results support the potential application of EB as a marine algae-derived functional material with relevance for both the food and pharmaceutical industries in the management of sleep disorders.

## Linked entities

- **Chemicals:** caffeine (PubChem CID 2519), malondialdehyde (PubChem CID 10964), γ-aminobutyric acid (PubChem CID 119), serotonin (PubChem CID 5202)
- **Diseases:** insomnia (MONDO:0013600)
- **Species:** Drosophila melanogaster (taxon 7227)

## Full-text entities

- **Diseases:** hyperactivity (MESH:D006948), Insomnia (MESH:D007319), sleep disorders (MESH:D012893), sleep fragmentation (MESH:D012892)
- **Chemicals:** BDZ (MESH:D001569), Eisenia bicyclis Extract (-), malondialdehyde (MESH:D008315), Caffeine (MESH:D002110), GABA (MESH:D005680), pentobarbital (MESH:D010424), serotonin (MESH:D012701)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Eisenia bicyclis (species) [taxon 6395], Drosophila melanogaster (fruit fly, species) [taxon 7227], PX clade (clade) [taxon 569578]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12603370/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12603370/full.md

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Source: https://tomesphere.com/paper/PMC12603370