Mergner T, Nasios G, Maurer C, Becker W
Neurologische Klinik, Universität Freiburg, Breisacherstr. 64, 79106 Freiburg, Germany.
Exp Brain Res. 2001 Nov;141(1):33-51. doi: 10.1007/s002210100826.
Perceptual updating of the location of visual targets in space after intervening eye, head or trunk movements requires an interaction between several afferent signals (visual, oculomotor efference copy, vestibular, proprioceptive). The nature of the interaction is still a matter of debate. To address this problem, we presented subjects (n=6) in the dark with a target (light spot) at various horizontal eccentricities (up to +/-20 degrees ) relative to the initially determined subjective straight-ahead direction (SSA). After a memory period of 12 s in complete darkness, the target reappeared at a random position and subjects were to reproduce its previous location in space using a remote control. For both the presentation and the reproduction of the target's location, subjects either kept their gaze in the SSA (retinal viewing condition) or fixated the eccentric target (visuo-oculomotor). Three experimental series were performed: A, "visual-only series": reproduction of the target's location in space was found to be close to ideal, independently of viewing condition; estimation curves (reproduced vs presented positions) showed intercepts approximately 0 degrees and slopes approximately 1; B, "visual-vestibular series": during the memory period, subjects were horizontally rotated to the right or left by 10 degrees or 18 degrees at 0.8-Hz or 0.1-Hz dominant frequency. Following the 0.8-Hz body rotation, reproduction was close to ideal, while at 0.1 Hz it was partially shifted along with the body, in line with the known vestibular high-pass characteristics. Additionally, eccentricity of target presentation reduced the slopes of the estimation curves (less than 1); C, "visual-vestibular-neck series": a shift toward the trunk also occurred after low-frequency neck stimulation (trunk rotated about stationary head). When vestibular and neck stimuli were combined (independent head and trunk rotations), their effects summed linearly, such that the errors cancelled each other during head rotation on the stationary trunk. Variability of responses was always lowest for targets presented at SSA, irrespective of intervening eye, head or trunk rotations. We conclude that: (1) subjects referenced "space" to pre-rotatory SSA and that the memory trace of the target's location in space was not altered during the memory period; and that (2) they used internal estimates of eye, head and trunk displacements with respect to space to match current target position with the memory trace during reproduction; these estimates would be obtained by inverting the physical coordinate transformations produced by these displacements. We present a model which is able to describe these operations and whose predictions closely parallel the experimental results. In this model the estimate of head rotation in space is not obtained directly from the vestibular head-in-space signal, but from a vestibular estimate of the kinematic state of the body support.
在眼睛、头部或躯干发生干预性运动后,对视觉目标在空间中位置的感知更新需要几种传入信号(视觉、动眼神经传出副本、前庭、本体感觉)之间的相互作用。这种相互作用的本质仍然存在争议。为了解决这个问题,我们让6名受试者在黑暗中面对一个目标(亮点),该目标相对于最初确定的主观正前方方向(SSA)具有不同的水平偏心率(最大可达±20度)。在完全黑暗中经过12秒的记忆期后,目标在一个随机位置重新出现,受试者要用遥控器再现其先前在空间中的位置。对于目标位置的呈现和再现,受试者要么将目光保持在SSA(视网膜观察条件),要么注视偏心目标(视觉 - 动眼神经)。进行了三个实验系列:A,“仅视觉系列”:发现目标在空间中位置的再现接近理想状态,与观察条件无关;估计曲线(再现位置与呈现位置)显示截距约为0度,斜率约为1;B,“视觉 - 前庭系列”:在记忆期内,受试者以0.8赫兹或0.1赫兹的主导频率水平向右或向左旋转10度或18度。在0.8赫兹的身体旋转后,再现接近理想状态,而在0.1赫兹时,它部分地随身体移动,这与已知的前庭高通特性一致。此外,目标呈现的偏心率降低了估计曲线的斜率(小于1);C,“视觉 - 前庭 - 颈部系列”:在低频颈部刺激(躯干围绕固定头部旋转)后也会出现向躯干的偏移。当前庭和颈部刺激相结合(头部和躯干独立旋转)时,它们的效果线性相加,使得在固定躯干上进行头部旋转时误差相互抵消。无论眼睛、头部或躯干如何旋转,在SSA呈现的目标的反应变异性总是最低的。我们得出以下结论:(1)受试者将“空间”参考为旋转前的SSA,并且目标在空间中位置的记忆痕迹在记忆期内没有改变;(2)他们在再现过程中使用眼睛、头部和躯干相对于空间位移的内部估计,以便将当前目标位置与记忆痕迹相匹配;这些估计将通过反转由这些位移产生的物理坐标变换来获得。我们提出了一个能够描述这些操作的模型,其预测与实验结果非常吻合。在这个模型中,空间中头部旋转的估计不是直接从空间中的前庭头部信号获得的,而是从身体支撑运动状态的前庭估计中获得的。