IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0163976.html
   My bibliography  Save this article

Pulsed Light Stimulation Increases Boundary Preference and Periodicity of Episodic Motor Activity in Drosophila melanogaster

Author

Listed:
  • Shuang Qiu
  • Chengfeng Xiao
  • R Meldrum Robertson

Abstract

There is considerable interest in the therapeutic benefits of long-term sensory stimulation for improving cognitive abilities and motor performance of stroke patients. The rationale is that such stimulation would activate mechanisms of neural plasticity to promote enhanced coordination and associated circuit functions. Experimental approaches to characterize such mechanisms are needed. Drosophila melanogaster is one of the most attractive model organisms to investigate neural mechanisms responsible for stimulation-induced behaviors with its powerful accessibility to genetic analysis. In this study, the effect of chronic sensory stimulation (pulsed light stimulation) on motor activity in w1118 flies was investigated. Flies were exposed to a chronic pulsed light stimulation protocol prior to testing their performance in a standard locomotion assay. Flies responded to pulsed light stimulation with increased boundary preference and travel distance in a circular arena. In addition, pulsed light stimulation increased the power of extracellular electrical activity, leading to the enhancement of periodic electrical activity which was associated with a centrally-generated motor pattern (struggling behavior). In contrast, such periodic events were largely missing in w1118 flies without pulsed light treatment. These data suggest that the sensory stimulation induced a response in motor activity associated with the modifications of electrical activity in the central nervous system (CNS). Finally, without pulsed light treatment, the wild-type genetic background was associated with the occurrence of the periodic activity in wild-type Canton S (CS) flies, and w+ modulated the consistency of periodicity. We conclude that pulsed light stimulation modifies behavioral and electrophysiological activities in w1118 flies. These data provide a foundation for future research on the genetic mechanisms of neural plasticity underlying such behavioral modification.

Suggested Citation

  • Shuang Qiu & Chengfeng Xiao & R Meldrum Robertson, 2016. "Pulsed Light Stimulation Increases Boundary Preference and Periodicity of Episodic Motor Activity in Drosophila melanogaster," PLOS ONE, Public Library of Science, vol. 11(9), pages 1-16, September.
  • Handle: RePEc:plo:pone00:0163976
    DOI: 10.1371/journal.pone.0163976
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0163976
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0163976&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0163976?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Maximiliano L. Suster & Michael Bate, 2002. "Embryonic assembly of a central pattern generator without sensory input," Nature, Nature, vol. 416(6877), pages 174-178, March.
    2. Chengfeng Xiao & R Meldrum Robertson, 2015. "Locomotion Induced by Spatial Restriction in Adult Drosophila," PLOS ONE, Public Library of Science, vol. 10(9), pages 1-19, September.
    3. Joan S. Steffan & Laszlo Bodai & Judit Pallos & Marnix Poelman & Alexander McCampbell & Barbara L. Apostol & Alexsey Kazantsev & Emily Schmidt & Ya-Zhen Zhu & Marilee Greenwald & Riki Kurokawa & David, 2001. "Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila," Nature, Nature, vol. 413(6857), pages 739-743, October.
    4. Pavan Ramdya & Pawel Lichocki & Steeve Cruchet & Lukas Frisch & Winnie Tse & Dario Floreano & Richard Benton, 2015. "Mechanosensory interactions drive collective behaviour in Drosophila," Nature, Nature, vol. 519(7542), pages 233-236, March.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Katerina Karkali & Samuel W. Vernon & Richard A. Baines & George Panayotou & Enrique Martín-Blanco, 2023. "Puckered and JNK signaling in pioneer neurons coordinates the motor activity of the Drosophila embryo," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    2. Joshua M Mueller & Primoz Ravbar & Julie H Simpson & Jean M Carlson, 2019. "Drosophila melanogaster grooming possesses syntax with distinct rules at different temporal scales," PLOS Computational Biology, Public Library of Science, vol. 15(6), pages 1-25, June.
    3. Antonella Cardinale & Emanuela Paldino & Carmela Giampà & Giorgio Bernardi & Francesca R Fusco, 2015. "PARP-1 Inhibition Is Neuroprotective in the R6/2 Mouse Model of Huntington’s Disease," PLOS ONE, Public Library of Science, vol. 10(8), pages 1-22, August.
    4. Thomas A. Verschut & Renny Ng & Nicolas P. Doubovetzky & Guillaume Calvez & Jan L. Sneep & Adriaan J. Minnaard & Chih-Ying Su & Mikael A. Carlsson & Bregje Wertheim & Jean-Christophe Billeter, 2023. "Aggregation pheromones have a non-linear effect on oviposition behavior in Drosophila melanogaster," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    5. William H Barnett & Gennady S Cymbalyuk, 2014. "A Codimension-2 Bifurcation Controlling Endogenous Bursting Activity and Pulse-Triggered Responses of a Neuron Model," PLOS ONE, Public Library of Science, vol. 9(1), pages 1-14, January.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0163976. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.