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Impaired trigeminal control of ingestive behavior in the Prrxl1- / - mouse is associated with a lemniscal-biased orosensory deafferentation

Admir Resulaj, Jeannette Wu, View ORCID ProfileMitra J. Z. Hartmann, Paul Feinstein, H. Phillip Zeigler
doi: https://doi.org/10.1101/2021.10.07.463562
Admir Resulaj
1Northwestern University Institute for Neuroscience, Northwestern University, Evanston, Illinois, 60208
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Jeannette Wu
2Department of Biomedical Engineering, Northwestern University, Evanston, Illinois, 60208
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Mitra J. Z. Hartmann
2Department of Biomedical Engineering, Northwestern University, Evanston, Illinois, 60208
3Department of Mechanical Engineering, Northwestern University, Evanston, Illinois, 60208
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  • ORCID record for Mitra J. Z. Hartmann
Paul Feinstein
4Department of Biological Sciences, Hunter College, City University of New York, New York, NY 10065
5The Graduate Center Programs in Biochemistry, Biology and CUNY Neuroscience Collaborative, 365 5th Ave, New York, NY 10016
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H. Phillip Zeigler
5The Graduate Center Programs in Biochemistry, Biology and CUNY Neuroscience Collaborative, 365 5th Ave, New York, NY 10016
6Department of Psychology, Hunter College, CUNY, New York, NY 10065
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  • For correspondence: mz7445@gmail.com
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Abstract

Although peripheral deafferentation studies have demonstrated a critical role for trigeminal afference in modulating the orosensorimotor control of eating and drinking, the central trigeminal pathways mediating that control, as well as the timescale of control, remain to be elucidated. In rodents, three ascending somatosensory pathways process and relay orofacial mechanosensory input: the lemniscal, paralemniscal, and extralemniscal. Two of these pathways (the lemniscal and extralemniscal) exhibit highly structured topographic representations of the orofacial sensory surface, as exemplified by the one-to-one somatotopic mapping between vibrissae on the animals’ face and barrelettes in brainstem, barreloids in thalamus, and barrels in cortex. Here we use the Prrxl1 knockout mouse model to investigate ingestive behavior deficits associated with disruption of the lemniscal pathway. The Prrxl1 deletion disrupts somatotopic patterning and axonal projections throughout the lemniscal pathway but spares patterning in the extralemniscal nucleus. Our data reveal an imprecise and inefficient ingestive phenotype with deficits that span timescales from milliseconds to months, tightly linking trigeminal input with ingestion, from moment-to-moment consummatory to long term appetitive control. We suggest that ordered assembly of trigeminal sensory information along the lemniscal pathway is critical for the rapid and precise modulation of motor circuits driving eating and drinking action sequences.

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 4.0 International license.
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Posted October 07, 2021.
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Impaired trigeminal control of ingestive behavior in the Prrxl1- / - mouse is associated with a lemniscal-biased orosensory deafferentation
Admir Resulaj, Jeannette Wu, Mitra J. Z. Hartmann, Paul Feinstein, H. Phillip Zeigler
bioRxiv 2021.10.07.463562; doi: https://doi.org/10.1101/2021.10.07.463562
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Impaired trigeminal control of ingestive behavior in the Prrxl1- / - mouse is associated with a lemniscal-biased orosensory deafferentation
Admir Resulaj, Jeannette Wu, Mitra J. Z. Hartmann, Paul Feinstein, H. Phillip Zeigler
bioRxiv 2021.10.07.463562; doi: https://doi.org/10.1101/2021.10.07.463562

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