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A cerebellar-prepontine circuit for tonic immobility triggered by an inescapable threat

Sudden changes in the environment are frequently perceived as threats and provoke defensive behavioral states. One such state is tonic immobility, a conserved defensive strategy characterized by powerful suppression of movement and motor reflexes. Tonic immobility has been associated with multiple b...

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Autores principales: Bhandiwad, Ashwin A., Chu, Nickolas C., Semenova, Svetlana A., Holmes, George A., Burgess, Harold A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519051/
https://www.ncbi.nlm.nih.gov/pubmed/36170356
http://dx.doi.org/10.1126/sciadv.abo0549
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author Bhandiwad, Ashwin A.
Chu, Nickolas C.
Semenova, Svetlana A.
Holmes, George A.
Burgess, Harold A.
author_facet Bhandiwad, Ashwin A.
Chu, Nickolas C.
Semenova, Svetlana A.
Holmes, George A.
Burgess, Harold A.
author_sort Bhandiwad, Ashwin A.
collection PubMed
description Sudden changes in the environment are frequently perceived as threats and provoke defensive behavioral states. One such state is tonic immobility, a conserved defensive strategy characterized by powerful suppression of movement and motor reflexes. Tonic immobility has been associated with multiple brainstem regions, but the underlying circuit is unknown. Here, we demonstrate that a strong vibratory stimulus evokes tonic immobility in larval zebrafish defined by suppressed locomotion and sensorimotor responses. Using a circuit-breaking screen and targeted neuron ablations, we show that cerebellar granule cells and a cluster of glutamatergic ventral prepontine neurons (vPPNs) that express key stress-associated neuropeptides are critical components of the circuit that suppresses movement. The complete sensorimotor circuit transmits information from sensory ganglia through the cerebellum to vPPNs to regulate reticulospinal premotor neurons. These results show that cerebellar regulation of a neuropeptide-rich prepontine structure governs a conserved and ancestral defensive behavior that is triggered by an inescapable threat.
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spelling pubmed-95190512022-10-13 A cerebellar-prepontine circuit for tonic immobility triggered by an inescapable threat Bhandiwad, Ashwin A. Chu, Nickolas C. Semenova, Svetlana A. Holmes, George A. Burgess, Harold A. Sci Adv Neuroscience Sudden changes in the environment are frequently perceived as threats and provoke defensive behavioral states. One such state is tonic immobility, a conserved defensive strategy characterized by powerful suppression of movement and motor reflexes. Tonic immobility has been associated with multiple brainstem regions, but the underlying circuit is unknown. Here, we demonstrate that a strong vibratory stimulus evokes tonic immobility in larval zebrafish defined by suppressed locomotion and sensorimotor responses. Using a circuit-breaking screen and targeted neuron ablations, we show that cerebellar granule cells and a cluster of glutamatergic ventral prepontine neurons (vPPNs) that express key stress-associated neuropeptides are critical components of the circuit that suppresses movement. The complete sensorimotor circuit transmits information from sensory ganglia through the cerebellum to vPPNs to regulate reticulospinal premotor neurons. These results show that cerebellar regulation of a neuropeptide-rich prepontine structure governs a conserved and ancestral defensive behavior that is triggered by an inescapable threat. American Association for the Advancement of Science 2022-09-28 /pmc/articles/PMC9519051/ /pubmed/36170356 http://dx.doi.org/10.1126/sciadv.abo0549 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Neuroscience
Bhandiwad, Ashwin A.
Chu, Nickolas C.
Semenova, Svetlana A.
Holmes, George A.
Burgess, Harold A.
A cerebellar-prepontine circuit for tonic immobility triggered by an inescapable threat
title A cerebellar-prepontine circuit for tonic immobility triggered by an inescapable threat
title_full A cerebellar-prepontine circuit for tonic immobility triggered by an inescapable threat
title_fullStr A cerebellar-prepontine circuit for tonic immobility triggered by an inescapable threat
title_full_unstemmed A cerebellar-prepontine circuit for tonic immobility triggered by an inescapable threat
title_short A cerebellar-prepontine circuit for tonic immobility triggered by an inescapable threat
title_sort cerebellar-prepontine circuit for tonic immobility triggered by an inescapable threat
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519051/
https://www.ncbi.nlm.nih.gov/pubmed/36170356
http://dx.doi.org/10.1126/sciadv.abo0549
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