FB2026_02 , released June 18, 2026
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Sun, X., Ran, D., Zhao, X., Huang, Y., Long, S., Liang, F., Guo, W., Nucifora, F.C., Gu, H., Lu, X., Chen, L., Zeng, J., Ross, C.A., Pei, Z. (2016). Melatonin attenuates hLRRK2-induced sleep disturbances and synaptic dysfunction in a Drosophila model of Parkinson's disease.  Mol. Med. Rep. 13(5): 3936--3944.
FlyBase ID
FBrf0232202
Publication Type
Research paper
Abstract
Sleep problems are the most common non-motor symptoms in Parkinson's disease (PD), and are more difficult to treat than the motor symptoms. In the current study, the role of human leucine-rich repeat kinase 2 (hLRRK2), the most common genetic cause of PD, was investigated with regards to sleep problems, and the therapeutic potential of melatonin in hLRRK2‑associated sleep problems was explored in Drosophila. hLRRK2 was selectively expressed in the mushroom bodies (MBs) in Drosophila and sleep patterns were measured using the Drosophila Activity Monitoring System. MB expression of hLRRK2 resulted in sleep problems, presynaptic dysfunction as evidenced by reduced miniature excitatory postsynaptic current (mEPSC) and excitatory postsynaptic potential (EPSP) frequency, and excessive synaptic plasticity such as increased axon bouton density. Treatment with melatonin at 4 mM significantly attenuated the sleep problems and rescued the reduction in mEPSC and EPSP frequency in the hLRRK2 transgenic flies. The present study demonstrates that MB expression of hLRRK2 in flies recapitulates the clinical features of the sleep disturbances in PD, and that melatonin attenuates hLRRK2-induced sleep disorders and synaptic dysfunction, suggesting the therapeutic potential of melatonin in PD patients carrying LRRK2 mutations.
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Mol. Med. Rep.
    Title
    Molecular medicine reports
    ISBN/ISSN
    1791-2997 1791-3004
    Data From Reference
    Alleles (3)
    Chemicals (1)
    Genes (2)
    Human Disease Models (1)
    Insertions (1)
    Transgenic Constructs (2)