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Mapping the signatures of inflammatory pain and its relief

Manon Bohic, Luke A. Pattison, Z. Anissa Jhumka, Heather Rossi, Joshua K. Thackray, Matthew Ricci, William Foster, Justin Arnold, Nahom Mossazghi, Max A. Tischfield, Eric A. Yttri, Ewan St. John Smith, Ishmail Abdus-Saboor, Victoria E. Abraira
doi: https://doi.org/10.1101/2021.06.16.448689
Manon Bohic
1Cell Biology and Neuroscience Department, Rutgers University, The State University of New Jersey, New Brunswick, United States of America
2W.M. Keck Center for Collaborative Neuroscience, Rutgers University, The State University of New Jersey, New Brunswick, United States of America
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Luke A. Pattison
3Department of Pharmacology, University of Cambridge, Cambridge, United Kingdom
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Z. Anissa Jhumka
4Zuckerman Mind Brain Behavior Institute and Department of Biological Sciences, Columbia University, New York, New York, United States of America
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Heather Rossi
4Zuckerman Mind Brain Behavior Institute and Department of Biological Sciences, Columbia University, New York, New York, United States of America
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Joshua K. Thackray
6Human Genetics Institute of New Jersey, Rutgers, The State University of New Jersey, Piscataway, NJ, United States of America
7Tourette International Collaborative Genetics Study (TIC Genetics)
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Matthew Ricci
8Data Science Initiative, Brown University, Providence, Rhode Island, United States
9School of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem, Israel
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William Foster
4Zuckerman Mind Brain Behavior Institute and Department of Biological Sciences, Columbia University, New York, New York, United States of America
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Justin Arnold
4Zuckerman Mind Brain Behavior Institute and Department of Biological Sciences, Columbia University, New York, New York, United States of America
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Nahom Mossazghi
10Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA, United States of America
11Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA, United States of America
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Max A. Tischfield
1Cell Biology and Neuroscience Department, Rutgers University, The State University of New Jersey, New Brunswick, United States of America
6Human Genetics Institute of New Jersey, Rutgers, The State University of New Jersey, Piscataway, NJ, United States of America
7Tourette International Collaborative Genetics Study (TIC Genetics)
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Eric A. Yttri
10Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA, United States of America
11Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA, United States of America
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Ewan St. John Smith
3Department of Pharmacology, University of Cambridge, Cambridge, United Kingdom
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Ishmail Abdus-Saboor
4Zuckerman Mind Brain Behavior Institute and Department of Biological Sciences, Columbia University, New York, New York, United States of America
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  • For correspondence: victoria.abraira@rutgers.edu ia2458@columbia.edu
Victoria E. Abraira
1Cell Biology and Neuroscience Department, Rutgers University, The State University of New Jersey, New Brunswick, United States of America
2W.M. Keck Center for Collaborative Neuroscience, Rutgers University, The State University of New Jersey, New Brunswick, United States of America
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  • For correspondence: victoria.abraira@rutgers.edu ia2458@columbia.edu
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Abstract

Ongoing pain is often driven by direct activation of pain-sensing neurons and neuroimmune mediated sensitization. These heightened states of pain alter physiology, reduce motor function, and alter motivation to engage in normal behaviors. The complexity of the pain state has evaded a comprehensive definition, especially in nonverbal animals. Here in mice, we capture the physiological state of sensitized pain neurons at different time points post-inflammation and used computational tools to automatically map behavioral signatures of evoked and spontaneous displays of pain. First, retrograde labeling coupled with electrophysiology of neurons innervating the site of localized inflammation defined critical time points of pain sensitization. Next, we used high-speed videography combined with supervised and unsupervised machine learning tools and uncovered sensory-evoked defensive coping postures to pain. Using 3D pose analytics inspired by natural language processing, we identify movement sequences that correspond to robust representations of ongoing pain states. Surprisingly, with this analytical framework, we find that a commonly used anti-inflammatory painkiller does not return an animal’s behavior back to a pre-injury state. Together, these findings reveal the previously unidentified signatures of pain and analgesia at timescales when inflammation induces heightened pain states.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted December 06, 2021.
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Mapping the signatures of inflammatory pain and its relief
Manon Bohic, Luke A. Pattison, Z. Anissa Jhumka, Heather Rossi, Joshua K. Thackray, Matthew Ricci, William Foster, Justin Arnold, Nahom Mossazghi, Max A. Tischfield, Eric A. Yttri, Ewan St. John Smith, Ishmail Abdus-Saboor, Victoria E. Abraira
bioRxiv 2021.06.16.448689; doi: https://doi.org/10.1101/2021.06.16.448689
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Mapping the signatures of inflammatory pain and its relief
Manon Bohic, Luke A. Pattison, Z. Anissa Jhumka, Heather Rossi, Joshua K. Thackray, Matthew Ricci, William Foster, Justin Arnold, Nahom Mossazghi, Max A. Tischfield, Eric A. Yttri, Ewan St. John Smith, Ishmail Abdus-Saboor, Victoria E. Abraira
bioRxiv 2021.06.16.448689; doi: https://doi.org/10.1101/2021.06.16.448689

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