Modeling eye-head gaze shifts in multiple contexts without motor planning

被引:7
|
作者
Haji-Abolhassani, Iman [1 ]
Guitton, Daniel [2 ]
Galiana, Henrietta L. [1 ]
机构
[1] McGill Univ, Dept Biomed Engn, Montreal, PQ, Canada
[2] Montreal Neurol Inst, Dept Neurol & Neurosurg, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
gaze shifts; common error feedback; eye-head coordination; vestibular compensation; saccade and fixation; network modeling; MONKEY SUPERIOR COLLICULUS; STEM OMNIPAUSE NEURONS; VESTIBULOOCULAR REFLEX SUPPRESSION; PREPOSITUS HYPOGLOSSI NEURONS; CAUDAL FASTIGIAL NUCLEUS; ALERT SQUIRREL-MONKEY; NECK MUSCLE RESPONSES; LEAD BURST NEURONS; BRAIN-STEM; REVERSIBLE INACTIVATION;
D O I
10.1152/jn.00605.2015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
During gaze shifts, the eyes and head collaborate to rapidly capture a target (saccade) and fixate it. Accordingly, models of gaze shift control should embed both saccadic and fixation modes and a mechanism for switching between them. We demonstrate a model in which the eye and head platforms are driven by a shared gaze error signal. To limit the number of free parameters, we implement a model reduction approach in which steady-state cerebellar effects at each of their projection sites are lumped with the parameter of that site. The model topology is consistent with anatomy and neurophysiology, and can replicate eye-head responses observed in multiple experimental contexts: 1) observed gaze characteristics across species and subjects can emerge from this structure with minor parametric changes; 2) gaze can move to a goal while in the fixation mode; 3) ocular compensation for head perturbations during saccades could rely on vestibular-only cells in the vestibular nuclei with postulated projections to burst neurons; 4) two nonlinearities suffice, i.e., the experimentally-determined mapping of tectoreticular cells onto brain stem targets and the increased recruitment of the head for larger target eccentricities; 5) the effects of initial conditions on eye/head trajectories are due to neural circuit dynamics, not planning; and 6) "compensatory" ocular slow phases exist even after semicircular canal plugging, because of interconnections linking eye-head circuits. Our model structure also simulates classical vestibulo-ocular reflex and pursuit nystagmus, and provides novel neural circuit and behavioral predictions, notably that both eye-head coordination and segmental limb coordination are possible without trajectory planning.
引用
收藏
页码:1956 / 1985
页数:30
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