Simvastatin modulates sleep-wake behavior and locomotor activity in a dose-dependent manner in Drosophila
2026 (English)In: Frontiers in Pharmacology, E-ISSN 1663-9812, Vol. 17, article id 1815042
Article in journal (Refereed) Published
Abstract [en]
Background: Statins, including simvastatin, are widely prescribed cholesterol-lowering drugs with well-established cardiovascular benefits, yet their potential neurobehavioral effects, including sleep disturbances, remain unclear. Because sleep regulation in Drosophila melanogaster is conserved with mammals, this model provides a powerful system to investigate drug-induced behavioral changes. Given the reported neurobehavioral effects of lipophilic statins, we hypothesized that simvastatin exposure would alter sleep-wake behavior and sleep architecture in D. melanogaster.
Methods: Wild-type flies were treated with simvastatin at concentrations of 0.00 (control), 0.05, 0.5, and 1.0 mM, and behavioral phenotypes were quantified.
Results: We observed a disruption of sleep architecture: 0.05 mM produced no detectable effect; 0.5 mM induced a robust insomnia-like phenotype characterized by reduced total sleep and prolonged sleep latency; whereas 1.0 mM increased arousal, enhancing wake activity and delaying sleep onset despite preserved total sleep amount.
Conclusion: These findings demonstrate that simvastatin exerts distinct, dose-dependent effects on sleep regulation, differentially affecting sleep initiation and maintenance. Collectively, this study suggests that Drosophila may serve as a useful model for investigating the behavioral effects of simvastatin, although further studies are required to validate and extend these observations.
Place, publisher, year, edition, pages
Frontiers Media S.A., 2026. Vol. 17, article id 1815042
Keywords [en]
behavioral pharmacology,
Drosophila, locomotor activity, simvastatin, sleep regulation
National Category
Neurosciences Pharmacology and Toxicology
Identifiers
URN: urn:nbn:se:uu:diva-594742DOI: 10.3389/fphar.2026.1815042ISI: 001820014800001PubMedID: 42460007OAI: oai:DiVA.org:uu-594742DiVA, id: diva2:2089119
2026-07-312026-07-312026-07-31Bibliographically approved