Self-generated Movements with "unexpected" Sensory Consequences
Overview
Affiliations
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.
Sensorimotor variability distinguishes early features of cognition in toddlers with autism.
Denisova K, Wolpert D iScience. 2024; 27(9):110685.
PMID: 39252975 PMC: 11381898. DOI: 10.1016/j.isci.2024.110685.
Early-life maturation of the somatosensory cortex: sensory experience and beyond.
Nwabudike I, Che A Front Neural Circuits. 2024; 18:1430783.
PMID: 39040685 PMC: 11260818. DOI: 10.3389/fncir.2024.1430783.
Activity-dependent dendrite patterning in the postnatal barrel cortex.
Nakagawa N, Iwasato T Front Neural Circuits. 2024; 18:1409993.
PMID: 38827189 PMC: 11140076. DOI: 10.3389/fncir.2024.1409993.
Neural decoding reveals specialized kinematic tuning after an abrupt cortical transition.
Glanz R, Sokoloff G, Blumberg M Cell Rep. 2023; 42(9):113119.
PMID: 37690023 PMC: 10591925. DOI: 10.1016/j.celrep.2023.113119.
Axonal connections between S1 barrel, M1, and S2 cortex in the newborn mouse.
Gellert L, Luhmann H, Kilb W Front Neuroanat. 2023; 17:1105998.
PMID: 36760662 PMC: 9905141. DOI: 10.3389/fnana.2023.1105998.