TY - JOUR
T1 - Multiple time courses of vestibular set-point adaptation revealed by sustained magnetic field stimulation of the labyrinth
AU - Jareonsettasin, Prem
AU - Otero-Millan, Jorge
AU - Ward, Bryan K.
AU - Roberts, Dale C.
AU - Schubert, Michael C.
AU - Zee, David S.
N1 - Funding Information:
This study was funded by NIH grants R21DC011919 and T32DC0000027 and by the Fight for Sight and Leon Levy Foundations. This work was made possible by support from the Brain-Science Institute of The Johns Hopkins University, The Johns Hopkins Medicine Discovery Fund, and the Cinquegrana, Lott, and Schwerin families.
Publisher Copyright:
© 2016 Elsevier Ltd.
PY - 2016/5/23
Y1 - 2016/5/23
N2 - A major focus in neurobiology is how the brain adapts its motor behavior to changes in its internal and external environments [1, 2]. Much is known about adaptively optimizing the amplitude and direction of eye and limb movements, for example, but little is known about another essential form of learning, "set-point" adaptation. Set-point adaptation balances tonic activity so that reciprocally acting, agonist and antagonist muscles have a stable platform from which to launch accurate movements. Here, we use the vestibulo-ocular reflex - a simple behavior that stabilizes the position of the eye while the head is moving - to investigate how tonic activity is adapted toward a new set point to prevent eye drift when the head is still [3, 4]. Set-point adaptation was elicited with magneto-hydrodynamic vestibular stimulation (MVS) by placing normal humans in a 7T MRI for 90 min. MVS is ideal for prolonged labyrinthine activation because it mimics constant head acceleration and induces a sustained nystagmus similar to natural vestibular lesions [5, 6]. The MVS-induced nystagmus diminished slowly but incompletely over multiple timescales. We propose a new adaptation hypothesis, using a cascade of imperfect mathematical integrators, that reproduces the response to MVS (and more natural chair rotations), including the gradual decrease in nystagmus as the set point changes over progressively longer time courses. MVS set-point adaptation is a biological model with applications to basic neurophysiological research into all types of movements [7], functional brain imaging [8], and treatment of vestibular and higher-level attentional disorders by introducing new biases to counteract pathological ones [9].
AB - A major focus in neurobiology is how the brain adapts its motor behavior to changes in its internal and external environments [1, 2]. Much is known about adaptively optimizing the amplitude and direction of eye and limb movements, for example, but little is known about another essential form of learning, "set-point" adaptation. Set-point adaptation balances tonic activity so that reciprocally acting, agonist and antagonist muscles have a stable platform from which to launch accurate movements. Here, we use the vestibulo-ocular reflex - a simple behavior that stabilizes the position of the eye while the head is moving - to investigate how tonic activity is adapted toward a new set point to prevent eye drift when the head is still [3, 4]. Set-point adaptation was elicited with magneto-hydrodynamic vestibular stimulation (MVS) by placing normal humans in a 7T MRI for 90 min. MVS is ideal for prolonged labyrinthine activation because it mimics constant head acceleration and induces a sustained nystagmus similar to natural vestibular lesions [5, 6]. The MVS-induced nystagmus diminished slowly but incompletely over multiple timescales. We propose a new adaptation hypothesis, using a cascade of imperfect mathematical integrators, that reproduces the response to MVS (and more natural chair rotations), including the gradual decrease in nystagmus as the set point changes over progressively longer time courses. MVS set-point adaptation is a biological model with applications to basic neurophysiological research into all types of movements [7], functional brain imaging [8], and treatment of vestibular and higher-level attentional disorders by introducing new biases to counteract pathological ones [9].
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U2 - 10.1016/j.cub.2016.03.066
DO - 10.1016/j.cub.2016.03.066
M3 - Article
C2 - 27185559
AN - SCOPUS:84966657878
SN - 0960-9822
VL - 26
SP - 1359
EP - 1366
JO - Current Biology
JF - Current Biology
IS - 10
ER -