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Self-generated Movements with "unexpected" Sensory Consequences

Overview
Journal Curr Biol
Publisher Cell Press
Specialty Biology
Date 2014 Aug 19
PMID 25131675
Citations 52
Authors
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Abstract

The nervous systems of diverse species, including worms and humans, possess mechanisms for distinguishing between sensations arising from self-generated (i.e., expected) movements from those arising from other-generated (i.e., unexpected) movements [1-3]. To make this critical distinction, animals generate copies, or corollary discharges, of motor commands [4, 5]. Corollary discharge facilitates the selective gating of reafferent signals arising from self-generated movements, thereby enhancing detection of novel stimuli [6-10]. However, for a developing nervous system, such sensory gating would be counterproductive if it impedes transmission of the very activity upon which activity-dependent mechanisms depend [11]. In infant rats during active (or REM) sleep--a behavioral state that predominates in early infancy [12-16]--neural circuits within the brainstem [17, 18] trigger hundreds of thousands of myoclonic twitches each day [19]. The putative contribution of these self-generated movements to the activity-dependent development of the sensorimotor system is supported by the observation that reafference from twitching limbs reliably and substantially triggers brain activity [20-23]. In contrast, under identical testing conditions, even the most vigorous wake movements reliably fail to trigger reafferent brain activity [21-23]. One hypothesis that accounts for this paradox is that twitches, uniquely among self-generated movements, lack corollary discharge [23]. Here, we test this hypothesis in newborn rats by manipulating the degree to which self-generated movements are expected and, therefore, their presumed recruitment of corollary discharge. We show that twitches, although self-generated, are processed as if they are unexpected.

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References
1.
Petersson P, Waldenstrom A, Fahraeus C, Schouenborg J . Spontaneous muscle twitches during sleep guide spinal self-organization. Nature. 2003; 424(6944):72-5. DOI: 10.1038/nature01719. View

2.
Kreider J, Blumberg M . Mesopontine contribution to the expression of active 'twitch' sleep in decerebrate week-old rats. Brain Res. 2000; 872(1-2):149-59. DOI: 10.1016/s0006-8993(00)02518-x. View

3.
Tiriac A, Uitermarkt B, Fanning A, Sokoloff G, Blumberg M . Rapid whisker movements in sleeping newborn rats. Curr Biol. 2012; 22(21):2075-80. PMC: 3494768. DOI: 10.1016/j.cub.2012.09.009. View

4.
Brooks J, Cullen K . The primate cerebellum selectively encodes unexpected self-motion. Curr Biol. 2013; 23(11):947-55. PMC: 6100740. DOI: 10.1016/j.cub.2013.04.029. View

5.
Seelke A, Blumberg M . The microstructure of active and quiet sleep as cortical delta activity emerges in infant rats. Sleep. 2008; 31(5):691-9. PMC: 2398759. DOI: 10.1093/sleep/31.5.691. View