Behrens F, Grüsser O J, Weiss L R
Universitätsklinikum Benjamin Franklin, Freie Universität Berlin, Department of Physiology, Germany.
Exp Brain Res. 1999 Feb;124(4):455-68. doi: 10.1007/s002210050641.
Eye position and angular velocity were measured in squirrel monkeys (Saimiri sciureus) by means of the electromagnetic scleral search-coil technique. Horizontal sigma-optokinetic nystagmus (sigma-OKN) was elicited by a stationary, stroboscopically illuminated, periodic, vertical-stripe pattern lining a vertical cylinder. The relationship between the mean slow-phase eye angular velocity, Ve, of sigma-OKN and the product of pattern period, Ps, and flash frequency, f(s), was determined. When Ve approximated k x Ps x f(s) (deg x s(-1)) and k was an integer > or = 1, the sigma-paradigm was fulfilled. Sigma-OKN could be evoked in different "modes", whereby k approximated 1, 2,...n. The sigma-OKN properties of squirrel monkeys were similar to those measured for sigma-OKN in the "stare" mode in man, with the exception of a long-lasting optokinetic afternystagmus (sigma-OKAN) appearing in the monkey. A considerable amount of temporal variability in flash sequence intervals ("temporal noise"), causing retinal error signals that interfered with the sigma-paradigm, was accepted by the visuo-motor system without interruption of sigma-OKN. This observation was explained by the operation of a short memory device for perception of visual motion. The internal gain, g(i), which relates the retinal "error" displacement velocity, Vr, and Ve depended, in turn, on Vr according to a function resembling the known relationship between neuronal activity of NOT (nucleus of the optic tract) nerve cells and Vr. This observation may be taken as direct proof that sigma-OKN can be explained by a centrally preprogrammed relationship between the retinal velocity, Vr, and the OKN slow-phase eye velocity, Ve. It is stipulated that the sum of Vr and efference copy signals generated in cortical or subcortical gaze centers is the essential component controlling the perceived velocity of the sigma-movement, whereby a short-term integrator plays a role for squirrel monkey sigma-OKN. When the flash frequency, f(s), was modulated periodically according to a sinewave or "triangular" function at a rate below 0.5 cycles x s(-1), Ve was found to respond with a corresponding modulation, provided the modulation amplitude did not exceed 50% of the mean flash rate. When the latter occurred, nonlinear responses could be observed. A similar response was found when the speed of "real" optokinetic stimuli was varied sinusoidally. Under these experimental conditions, however, the amplitude of the Ve variation yielded up to 1.0 approximately linear responses.
通过电磁巩膜搜索线圈技术测量松鼠猴(松鼠猴)的眼位和角速度。水平西格玛视动性眼震(西格玛 - OKN)由固定的、频闪照明的、周期性的垂直条纹图案诱发,该图案排列在一个垂直圆柱体上。确定了西格玛 - OKN的平均慢相眼角速度Ve与图案周期Ps和闪光频率f(s)的乘积之间的关系。当Ve近似于k×Ps×f(s)(度×秒⁻¹)且k为大于或等于1的整数时,满足西格玛范式。西格玛 - OKN可以在不同的“模式”下诱发,其中k近似于1、2……n。松鼠猴的西格玛 - OKN特性与人类“凝视”模式下测量的西格玛 - OKN特性相似,但猴子会出现持续时间较长的视动后眼震(西格玛 - OKAN)。视觉运动系统接受了相当数量的闪光序列间隔中的时间变异性(“时间噪声”),这种变异性会产生干扰西格玛范式的视网膜误差信号,但不会中断西格玛 - OKN。这一观察结果通过一个用于感知视觉运动的短记忆装置的运作得到了解释。将视网膜“误差”位移速度Vr与Ve相关联的内部增益g(i),又根据一个类似于已知视束核(NOT)神经细胞的神经元活动与Vr之间关系的函数,依赖于Vr。这一观察结果可被视为西格玛 - OKN可以通过视网膜速度Vr与OKN慢相眼速度Ve之间的中枢预编程关系来解释的直接证据。规定Vr与在皮层或皮层下注视中心产生的传出副本信号之和是控制西格玛运动感知速度的基本组成部分,其中一个短期积分器对松鼠猴的西格玛 - OKN起作用。当闪光频率f(s)以低于0.5周期×秒⁻¹的速率根据正弦波或“三角形”函数进行周期性调制时,发现Ve会以相应的调制做出响应,前提是调制幅度不超过平均闪光速率的50%。当出现后者情况时,可以观察到非线性响应。当“真实”视动刺激的速度以正弦形式变化时,也发现了类似的响应。然而,在这些实验条件下,Ve变化的幅度产生了高达1.0的近似线性响应。