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Spontaneous activity and functional connectivity in the developing cerebellorubral system
Journal article   Open access   Peer reviewed

Spontaneous activity and functional connectivity in the developing cerebellorubral system

Carlos Del Rio-Bermudez, Alan M Plumeau, Nicholas J Sattler, Greta Sokoloff and Mark S Blumberg
Journal of neurophysiology, Vol.116(3), pp.1316-1327
09/01/2016
DOI: 10.1152/jn.00461.2016
PMCID: PMC5023414
PMID: 27385801
url
https://doi.org/10.1152/jn.00461.2016View
Published (Version of record) Open Access

Abstract

The development of the cerebellar system depends in part on the emergence of functional connectivity in its input and output pathways. Characterization of spontaneous activity within these pathways provides insight into their functional status in early development. In the present study we recorded extracellular activity from the interpositus nucleus (IP) and its primary downstream target, the red nucleus (RN), in unanesthetized rats at postnatal days 8 (P8) and P12, a period of dramatic change in cerebellar circuitry. The two structures exhibited state-dependent activity patterns and age-related changes in rhythmicity and overall firing rate. Importantly, sensory feedback (i.e., reafference) from myoclonic twitches (spontaneous, self-generated movements that are produced exclusively during active sleep) drove neural activity in the IP and RN at both ages. Additionally, anatomic tracing confirmed the presence of cerebellorubral connections as early as P8. Finally, inactivation of the IP and adjacent nuclei using the GABAA receptor agonist muscimol caused a substantial decrease in neural activity in the contralateral RN at both ages, as well as the disappearance of rhythmicity; twitch-related activity in the RN, however, was preserved after IP inactivation, indicating that twitch-related reafference activates the two structures in parallel. Overall, the present findings point to the contributions of sleep-related spontaneous activity to the development of cerebellar networks.
Muscimol - pharmacology Neural Pathways - drug effects Cerebellum - drug effects Red Nucleus - physiology Male Neurons - cytology Cerebellum - physiology Neural Pathways - physiology Movement - physiology GABA-A Receptor Agonists - pharmacology Neurons - physiology Female Electromyography Neurons - drug effects Action Potentials - drug effects Microelectrodes Movement - drug effects Neural Pathways - growth & development Periodicity Rats, Sprague-Dawley Action Potentials - physiology Red Nucleus - cytology Red Nucleus - growth & development Animals Red Nucleus - drug effects Cerebellum - cytology Neural Pathways - cytology Cerebellum - growth & development Receptors, GABA-A - metabolism

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