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    The NCA sodium leak channel is required for persistent motor circuit activity that sustains locomotion

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    Authors
    Gao, Shangbang
    Xie, Lin
    Kawano, Taizo
    Po, Michelle D.
    Guan, Sihui
    Zhen, Mei
    Pirri, Jennifer K.
    Alkema, Mark J
    UMass Chan Affiliations
    Graduate School of Biomedical Sciences, Neuroscience Program
    Alkema Lab
    Neurobiology
    Document Type
    Journal Article
    Publication Date
    2015-02-26
    Keywords
    Neural circuits
    Sodium channels
    Working memory
    Neuroscience and Neurobiology
    
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    Link to Full Text
    http://dx.doi.org/10.1038/ncomms7323
    Abstract
    Persistent neural activity, a sustained circuit output that outlasts the stimuli, underlies short-term or working memory, as well as various mental representations. Molecular mechanisms that underlie persistent activity are not well understood. Combining in situ whole-cell patch clamping and quantitative locomotion analyses, we show here that the Caenorhabditis elegans neuromuscular system exhibits persistent rhythmic activity, and such an activity contributes to the sustainability of basal locomotion, and the maintenance of acceleration after stimulation. The NALCN family sodium leak channel regulates the resting membrane potential and excitability of invertebrate and vertebrate neurons. Our molecular genetics and electrophysiology analyses show that the C. elegans NALCN, NCA, activates a premotor interneuron network to potentiate persistent motor circuit activity and to sustain C. elegans locomotion. Collectively, these results reveal a mechanism for, and physiological function of, persistent neural activity using a simple animal model, providing potential mechanistic clues for working memory in other systems.
    Source
    Nat Commun. 2015 Feb 26;6:6323. doi: 10.1038/ncomms7323.
    DOI
    10.1038/ncomms7323
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/37915
    PubMed ID
    25716181
    Notes

    Co-author Jennifer Pirri is a doctoral student in the Neuroscience Program in the Graduate School of Biomedical Sciences (GSBS) at UMass Medical School.

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    Link to article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1038/ncomms7323
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