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Effects of <i>Eisenia bicyclis</i> Extract on Sleep Promotion in a Caffeine-Induced Insomnia Models.

Journal of microbiology and biotechnology2025Ha YJ, Lee S, Suh HJ, et al.
Study designOther primary literature
SubjectAnimal

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.

MeSH

AnimalsAntioxidantsBrainCaffeineDisease Models, AnimalDrosophila melanogasterEdible SeaweedsKelpMaleMalondialdehydeMiceMice, Inbred ICRPhaeophyceaePlant ExtractsSerotoninSleepSleep Initiation and Maintenance Disordersgamma-Aminobutyric Acid

DOI 10.4014/jmb.2509.09008

PMID 41162163

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