Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice. / Bellardita, Carmelo; Caggiano, Vittorio; Leiras, Roberto; Caldeira, Vanessa; Fuchs, Andrea; Bouvier, Julien; Löw, Peter; Kiehn, Ole.

In: eLife, Vol. 6, e23011, 13.02.2017.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Bellardita, C, Caggiano, V, Leiras, R, Caldeira, V, Fuchs, A, Bouvier, J, Löw, P & Kiehn, O 2017, 'Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice', eLife, vol. 6, e23011. https://doi.org/10.7554/eLife.23011

APA

Bellardita, C., Caggiano, V., Leiras, R., Caldeira, V., Fuchs, A., Bouvier, J., Löw, P., & Kiehn, O. (2017). Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice. eLife, 6, [e23011]. https://doi.org/10.7554/eLife.23011

Vancouver

Bellardita C, Caggiano V, Leiras R, Caldeira V, Fuchs A, Bouvier J et al. Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice. eLife. 2017 Feb 13;6. e23011. https://doi.org/10.7554/eLife.23011

Author

Bellardita, Carmelo ; Caggiano, Vittorio ; Leiras, Roberto ; Caldeira, Vanessa ; Fuchs, Andrea ; Bouvier, Julien ; Löw, Peter ; Kiehn, Ole. / Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice. In: eLife. 2017 ; Vol. 6.

Bibtex

@article{2a2e1203df6b476a8244c9a80345d231,
title = "Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice",
abstract = "Spasms after spinal cord injury (SCI) are debilitating involuntary muscle contractions that have been associated with increased motor neuron excitability and decreased inhibition. However, whether spasms involve activation of premotor spinal excitatory neuronal circuits is unknown. Here we use mouse genetics, electrophysiology, imaging and optogenetics to directly target major classes of spinal interneurons as well as motor neurons during spasms in a mouse model of chronic SCI. We find that assemblies of excitatory spinal interneurons are recruited by sensory input into functional circuits to generate persistent neural activity, which interacts with both the graded expression of plateau potentials in motor neurons to generate spasms, and inhibitory interneurons to curtail them. Our study reveals hitherto unrecognized neuronal mechanisms for the generation of persistent neural activity under pathophysiological conditions, opening up new targets for treatment of muscle spasms after SCI.",
author = "Carmelo Bellardita and Vittorio Caggiano and Roberto Leiras and Vanessa Caldeira and Andrea Fuchs and Julien Bouvier and Peter L{\"o}w and Ole Kiehn",
year = "2017",
month = feb,
day = "13",
doi = "10.7554/eLife.23011",
language = "English",
volume = "6",
journal = "eLife",
issn = "2050-084X",
publisher = "eLife Sciences Publications Ltd.",

}

RIS

TY - JOUR

T1 - Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice

AU - Bellardita, Carmelo

AU - Caggiano, Vittorio

AU - Leiras, Roberto

AU - Caldeira, Vanessa

AU - Fuchs, Andrea

AU - Bouvier, Julien

AU - Löw, Peter

AU - Kiehn, Ole

PY - 2017/2/13

Y1 - 2017/2/13

N2 - Spasms after spinal cord injury (SCI) are debilitating involuntary muscle contractions that have been associated with increased motor neuron excitability and decreased inhibition. However, whether spasms involve activation of premotor spinal excitatory neuronal circuits is unknown. Here we use mouse genetics, electrophysiology, imaging and optogenetics to directly target major classes of spinal interneurons as well as motor neurons during spasms in a mouse model of chronic SCI. We find that assemblies of excitatory spinal interneurons are recruited by sensory input into functional circuits to generate persistent neural activity, which interacts with both the graded expression of plateau potentials in motor neurons to generate spasms, and inhibitory interneurons to curtail them. Our study reveals hitherto unrecognized neuronal mechanisms for the generation of persistent neural activity under pathophysiological conditions, opening up new targets for treatment of muscle spasms after SCI.

AB - Spasms after spinal cord injury (SCI) are debilitating involuntary muscle contractions that have been associated with increased motor neuron excitability and decreased inhibition. However, whether spasms involve activation of premotor spinal excitatory neuronal circuits is unknown. Here we use mouse genetics, electrophysiology, imaging and optogenetics to directly target major classes of spinal interneurons as well as motor neurons during spasms in a mouse model of chronic SCI. We find that assemblies of excitatory spinal interneurons are recruited by sensory input into functional circuits to generate persistent neural activity, which interacts with both the graded expression of plateau potentials in motor neurons to generate spasms, and inhibitory interneurons to curtail them. Our study reveals hitherto unrecognized neuronal mechanisms for the generation of persistent neural activity under pathophysiological conditions, opening up new targets for treatment of muscle spasms after SCI.

U2 - 10.7554/eLife.23011

DO - 10.7554/eLife.23011

M3 - Journal article

C2 - 28191872

AN - SCOPUS:85014439465

VL - 6

JO - eLife

JF - eLife

SN - 2050-084X

M1 - e23011

ER -

ID: 194975924