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短潜伏期视差辐辏反应及其对先前眼球扫视运动的依赖性。

Short-latency disparity vergence responses and their dependence on a prior saccadic eye movement.

作者信息

Busettini C, Miles F A, Krauzlis R J

机构信息

Laboratory of Sensorimotor Research, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

J Neurophysiol. 1996 Apr;75(4):1392-410. doi: 10.1152/jn.1996.75.4.1392.

Abstract
  1. A dichoptic viewing arrangement was used to study the initial vergence eye movements elicited by brief horizontal disparity steps applied to large textured patterns in three rhesus monkeys. Disconjugate steps (range, 0.2-10.9 degrees) were applied to the patterns at selected times (range, 13-303 ms) after 10 degrees leftward saccades into the center of the pattern. The horizontal and vertical positions of both eyes were recorded with the electromagnetic search coil technique. 2. Without training or reinforcement, disparity steps of suitable amplitude consistently elicited vergence responses at short latencies. For example, with 1.8 degrees crossed-disparity steps applied 26 ms after the centering saccade, the mean latency of onset of convergence for each of the three monkeys was 52.2 +/- 3.8 (SD) ms, 52.3 +/- 5.2 ms, and 53.4 +/- 4.1 ms. 3. Experiments in which the disparity step was confined to only one eye indicated that each eye was not simply tracking the apparent motion that is saw. For example, when crossed-disparity steps were confined to the right eye (which saw leftward steps), the result was (binocular) convergence in which the left eye moved to the right even though that eye had seen only a stationary scene. This movement of the left eye cannot have resulted from independent monocular tracking and indicates that the vergences here derived from the binocular misalignment of the two retinal images. 4. The initial vergence responses to crossed-disparity steps had the following main features. 1) They were always in the correct (i.e., convergent) direction over the full range of stimuli tested, the initial vergence acceleration increasing progressively with increases in disparity until reaching a peak with steps of 1.4-2.4 degrees and declining thereafter to a nonzero asymptote as steps exceeded 5-7 degrees. 2) They showed transient postsaccadic enhancement whereby steps applied in the immediate wake of a saccadic eye movement resulted in much higher initial vergence accelerations than the same steps applied some time later. The response decline in the wake of a saccade was roughly exponential with time constants of 67 +/- 5 (SD) ms, 35 +/- 2 ms, and 54 +/- 4 ms for the three animals. 3) That the postsaccadic enhancement might have resulted in part from the visual stimulation associated with the prior saccade was suggested by the finding that enhancement could also be observed when the disparity steps were applied in the wake of (conjugate) saccadelike shifts of the textured pattern. However, this visual enhancement did not reach a peak unit 17-37 ms after the end of the "simulated" saccade, and the peak enhancement averaged only 45% of that after a "real" saccade. 4) Qualitatively similar transient enhancements in the wake of real and simulated saccades have also been reported for initial ocular following responses elicited by conjugate drifts of the visual scene. We replicated the enhancement effects on ocular following to allow a direct comparison with the enhancement effects on disparity vergence using the same animals and visual stimulus patterns and, despite some clear quantitative differences, we suggest that the enhancement effects share a similar etiology. 5. Initial vergence responses to uncrossed-disparity steps had the following main features. 1) They were in the correct (i.e., divergent) direction only for very small steps (< 1.5-2.5 degrees), and then only when postsaccadic delays were small; when the magnitude of the steps was increased beyond these levels, responses declined to zero and thereafter reversed direction, eventually reaching a nonzero (convergent) asymptote similar to that seen with large crossed-disparity steps; convergent responses were also seen with larger vertical disparity steps, suggesting that they represent default responses to any disparity exceeding a few degrees. 2) As the postsaccadic delay was increased, responses to small steps (1.8 degrees) declined to zero and thereafter re
摘要
  1. 采用双眼分视观察装置,研究了三只恒河猴在向大纹理图案中心进行10度向左扫视后,在选定时间(范围为13 - 303毫秒)施加短暂水平视差阶跃所引发的初始辐辏眼动。在扫视进入图案中心后,向图案施加非共轭阶跃(范围为0.2 - 10.9度)。双眼的水平和垂直位置通过电磁搜索线圈技术进行记录。2. 未经训练或强化,合适幅度的视差阶跃在短潜伏期内始终能引发辐辏反应。例如,在对中扫视后26毫秒施加1.8度的交叉视差阶跃,三只猴子各自的会聚起始平均潜伏期分别为52.2 +/- 3.8(标准差)毫秒、52.3 +/- 5.2毫秒和53.4 +/- (标准差)4.1毫秒。3. 将视差阶跃仅局限于一只眼睛的实验表明,每只眼睛并非简单地追踪所看到的表观运动。例如,当交叉视差阶跃局限于右眼(看到向左的阶跃)时,结果是(双眼)会聚,其中左眼向右移动,尽管那只眼睛只看到了静止的场景。左眼的这种运动不可能是由独立的单眼追踪导致的,这表明此处的辐辏源自两个视网膜图像的双眼视差不对准。4.对交叉视差阶跃的初始辐辏反应具有以下主要特征。1)在测试的整个刺激范围内,它们始终处于正确(即会聚)方向,初始辐辏加速度随着视差增加而逐渐增大,直到视差为1.4 - 2.4度的阶跃时达到峰值,此后随着视差超过5 - 7度而下降至非零渐近线。2)它们表现出扫视后瞬态增强,即在眼球扫视运动后立即施加的阶跃导致的初始辐辏加速度比稍后施加相同阶跃时高得多。三只动物在扫视后的反应下降大致呈指数形式,时间常数分别为67 +/- 5(标准差)毫秒、35 +/- 2毫秒和54 +/- 4毫秒。3)当视差阶跃在纹理图案的(共轭)类似扫视位移之后施加时也能观察到增强,这表明扫视后增强可能部分源于与先前扫视相关的视觉刺激。然而,这种视觉增强在“模拟”扫视结束后17 - 37毫秒才达到峰值,且峰值增强平均仅为“真实”扫视后的45%。4)对于视觉场景共轭漂移引发的初始眼球跟随反应,在真实和模拟扫视后也有定性相似的瞬态增强报道。我们重复了对眼球跟随的增强效应,以便使用相同的动物和视觉刺激模式与对视差辐辏的增强效应进行直接比较,尽管存在一些明显的定量差异,但我们认为增强效应具有相似的病因。5.对非交叉视差阶跃的初始辐辏反应具有以下主要特征。1)仅在非常小的阶跃(<1.5 - 2.5度)时,且仅在扫视后延迟较小时,它们才处于正确(即发散)方向;当阶跃幅度超过这些水平时,反应下降至零,此后反转方向,最终达到与大交叉视差阶跃时类似的非零(会聚)渐近线;较大的垂直视差阶跃也会出现会聚反应,这表明它们代表对任何超过几度视差的默认反应。2)随着扫视后延迟增加,对小阶跃(1.8度)的反应下降至零,此后重新……

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