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Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2022.10.28.514163v1?rss=1
Authors: Broersen, R., Carulli, D., Canto, C. B., De Zeeuw, C. I.
Abstract:
Learning to associate a cue with its aversive consequence enables animals to prevent harm. Associative conditioning relies on activity within the cerebellum, but little is known about how changes in synaptic inputs to its output neurons shape their membrane potential dynamics during learning. Here we studied these changes in inputs using whole-cell and juxtasomal recordings of cerebellar nucleus neurons in awake mice during eyeblink conditioning and doing post-learning structural analysis. We identified changes in mossy fiber- and Purkinje cell-, but not climbing fiber-, inputs, leading to changes in subthreshold processing that correlate with the level and direction of the conditioned eyelid movements. These changes appear sufficient, as optogenetic stimulation of the inputs evoke incremental eyelid closures over the course of conditioning. Our data reveal how electrophysiological and structural modifications at the level of synaptic inputs to cerebellar output neurons facilitate conditioning of eyelid movements.
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http://biorxiv.org/cgi/content/short/2022.10.28.514163v1?rss=1
Authors: Broersen, R., Carulli, D., Canto, C. B., De Zeeuw, C. I.
Abstract:
Learning to associate a cue with its aversive consequence enables animals to prevent harm. Associative conditioning relies on activity within the cerebellum, but little is known about how changes in synaptic inputs to its output neurons shape their membrane potential dynamics during learning. Here we studied these changes in inputs using whole-cell and juxtasomal recordings of cerebellar nucleus neurons in awake mice during eyeblink conditioning and doing post-learning structural analysis. We identified changes in mossy fiber- and Purkinje cell-, but not climbing fiber-, inputs, leading to changes in subthreshold processing that correlate with the level and direction of the conditioned eyelid movements. These changes appear sufficient, as optogenetic stimulation of the inputs evoke incremental eyelid closures over the course of conditioning. Our data reveal how electrophysiological and structural modifications at the level of synaptic inputs to cerebellar output neurons facilitate conditioning of eyelid movements.
Copy rights belong to original authors. Visit the link for more info
Podcast created by Paper Player, LLC
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Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2022.12.30.522096v1?rss=1
Authors: Whitmarsh, S., Nguyen-Michel, V.-H., Lehongre, K., Mathon, B., Adam, C., Lambrecq, V. L., Frazzini, V., Navarro, V.
Abstract:
Epileptic seizures and interictal epileptiform discharges (IEDs) are stron…
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2022.12.30.522289v1?rss=1
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Abstract:
Adolescent cocaine exposure (ACE) induce anxiety and higher sensitivity to dru…
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2022.12.29.522264v1?rss=1
Authors: Kleinfeld, D., Liao, S.-M.
Abstract:
The breathing rhythm serves as a reference that paces orofacial motor actions and orchestrates active sensing. Past work reports that pacing occurs solely at a fix…
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2022.12.28.522095v1?rss=1
Authors: Melo, M. R., Wykes, A. D., Connelly, A. A., Bassi, J. K., Cheung, S. D., McDougall, S. J., Menuet, C., Bathgate, R. A., Allen, A. M.
Abstract:
The preBotzinger Complex (preBotC), a key primary generat…
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2022.12.30.522216v1?rss=1
Authors: Regev, T. I., Casto, C., Hosseini, E. A., Adamek, M., Brunner, P., Fedorenko, E.
Abstract:
A left-lateralized network of frontal and temporal brain regions is specialized for language processing-spoke…
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