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ZENODO
Dataset . 2023
License: CC BY
Data sources: Datacite
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ZENODO
Dataset . 2023
License: CC BY
Data sources: Datacite
image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
ZENODO
Dataset . 2023
License: CC BY
Data sources: ZENODO
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Mapping the neuroethological signatures of pain, analgesia and recovery in mice

Authors: Bohic, Manon; Pattison, Luke A.; Jhumka, Z. Anissa; Rossi, Heather; Thackray, Joshua K.; Ricci, Matthew; Mossazghi, Nahom; +10 Authors

Mapping the neuroethological signatures of pain, analgesia and recovery in mice

Abstract

Mapping the neuroethological signatures of pain, analgesia and recovery in mice. Repository containing datasets obtained for M. Bohic, L Pattison, et al. 2023. Neuron. Abstract Ongoing pain is driven by direct activation of pain-sensing neurons and neuroimmune mediated sensitization. These heightened pain states alter physiology, reduce motor function, and affect 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 neurons and use computational tools to automatically map behavioral signatures of evoked and spontaneous displays of pain at different time points for both an acute model of paw inflammatory pain and a chronic model of knee joint pain. First, retrograde labeling coupled with electrophysiology of neurons innervating injury sites revealed key time points corresponding to peripheral sensitivity in multiple pain models. Next, we used high-speed videography combined with supervised and unsupervised machine learning tools to uncover sensory-evoked defensive coping postures, unique to each pain condition. Using 3D pose analytics inspired by natural language processing, we identify movement sequences that correspond to robust representations of ongoing pain states. With this new analytical framework, we find that commonly used analgesics do not return an animal’s behavior to a pre-injury state. Instead, animals adopt a novel set of spontaneous behaviors that are maintained even after most evoked behavioral features of pain have resolved. Together, these findings reveal previously unidentified neuroethological signatures of pain and analgesia at timescales when inflammation induces heightened pain states and during recovery.

Keywords

behavior, analgesia, electrophysiology, recovery, machine learning, inflammation, carrageenan, pain, nociception, osteoarthritis;, allodynia, hyperalgesia

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selected citations
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
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