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An output-null signature of inertial load in motor cortex

Author

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  • Eric A. Kirk

    (Case Western Reserve University School of Medicine)

  • Keenan T. Hope

    (Case Western Reserve University School of Medicine)

  • Samuel J. Sober

    (Emory University)

  • Britton A. Sauerbrei

    (Case Western Reserve University School of Medicine)

Abstract

Coordinated movement requires the nervous system to continuously compensate for changes in mechanical load across different conditions. For voluntary movements like reaching, the motor cortex is a critical hub that generates commands to move the limbs and counteract loads. How does cortex contribute to load compensation when rhythmic movements are sequenced by a spinal pattern generator? Here, we address this question by manipulating the mass of the forelimb in unrestrained mice during locomotion. While load produces changes in motor output that are robust to inactivation of motor cortex, it also induces a profound shift in cortical dynamics. This shift is minimally affected by cerebellar perturbation and significantly larger than the load response in the spinal motoneuron population. This latent representation may enable motor cortex to generate appropriate commands when a voluntary movement must be integrated with an ongoing, spinally-generated rhythm.

Suggested Citation

  • Eric A. Kirk & Keenan T. Hope & Samuel J. Sober & Britton A. Sauerbrei, 2024. "An output-null signature of inertial load in motor cortex," Nature Communications, Nature, vol. 15(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-51750-7
    DOI: 10.1038/s41467-024-51750-7
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    References listed on IDEAS

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    1. Nuo Li & Kayvon Daie & Karel Svoboda & Shaul Druckmann, 2016. "Robust neuronal dynamics in premotor cortex during motor planning," Nature, Nature, vol. 532(7600), pages 459-464, April.
    2. Henrik Lindén & Peter C. Petersen & Mikkel Vestergaard & Rune W. Berg, 2022. "Movement is governed by rotational neural dynamics in spinal motor networks," Nature, Nature, vol. 610(7932), pages 526-531, October.
    3. Nuo Li & Kayvon Daie & Karel Svoboda & Shaul Druckmann, 2016. "Correction: Corrigendum: Robust neuronal dynamics in premotor cortex during motor planning," Nature, Nature, vol. 537(7618), pages 122-122, September.
    4. Zhenyu Gao & Courtney Davis & Alyse M. Thomas & Michael N. Economo & Amada M. Abrego & Karel Svoboda & Chris I. Zeeuw & Nuo Li, 2018. "A cortico-cerebellar loop for motor planning," Nature, Nature, vol. 563(7729), pages 113-116, November.
    5. Paolo Capelli & Chiara Pivetta & Maria Soledad Esposito & Silvia Arber, 2017. "Locomotor speed control circuits in the caudal brainstem," Nature, Nature, vol. 551(7680), pages 373-377, November.
    6. V. Caggiano & R. Leiras & H. Goñi-Erro & D. Masini & C. Bellardita & J. Bouvier & V. Caldeira & G. Fisone & O. Kiehn, 2018. "Midbrain circuits that set locomotor speed and gait selection," Nature, Nature, vol. 553(7689), pages 455-460, January.
    7. Zengcai V. Guo & Hidehiko K. Inagaki & Kayvon Daie & Shaul Druckmann & Charles R. Gerfen & Karel Svoboda, 2017. "Maintenance of persistent activity in a frontal thalamocortical loop," Nature, Nature, vol. 545(7653), pages 181-186, May.
    8. Ignacio Alonso & Irina Scheer & Mélanie Palacio-Manzano & Noémie Frézel-Jacob & Antoine Philippides & Mario Prsa, 2023. "Peripersonal encoding of forelimb proprioception in the mouse somatosensory cortex," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    9. Xulu Sun & Daniel J. O’Shea & Matthew D. Golub & Eric M. Trautmann & Saurabh Vyas & Stephen I. Ryu & Krishna V. Shenoy, 2022. "Cortical preparatory activity indexes learned motor memories," Nature, Nature, vol. 602(7896), pages 274-279, February.
    10. Britton A. Sauerbrei & Jian-Zhong Guo & Jeremy D. Cohen & Matteo Mischiati & Wendy Guo & Mayank Kabra & Nakul Verma & Brett Mensh & Kristin Branson & Adam W. Hantman, 2020. "Cortical pattern generation during dexterous movement is input-driven," Nature, Nature, vol. 577(7790), pages 386-391, January.
    11. Gamaleldin F. Elsayed & Antonio H. Lara & Matthew T. Kaufman & Mark M. Churchland & John P. Cunningham, 2016. "Reorganization between preparatory and movement population responses in motor cortex," Nature Communications, Nature, vol. 7(1), pages 1-15, December.
    12. Mark M. Churchland & John P. Cunningham & Matthew T. Kaufman & Justin D. Foster & Paul Nuyujukian & Stephen I. Ryu & Krishna V. Shenoy, 2012. "Neural population dynamics during reaching," Nature, Nature, vol. 487(7405), pages 51-56, July.
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