Dieringer N, Precht W
Exp Brain Res. 1982;47(3):394-406. doi: 10.1007/BF00239357.
Compensatory head movements, recorded in unrestrained frogs, were compared to compensatory eye movements recorded from animals that had their head fixed. Movements were evoked by oscillating the animal in the dark (vestibular stimulation) or in the light in front of an earth-fixed, patterned visual background (combined stimulation) or by rotating vertical black and white bars (optokinetic stimulation) around the stationary animal. Oscillations occurred in the horizontal plane at frequencies between 0.025 and 0.5 Hz. Gain and phase values of head and eye movements, relative to stimulus movements were calculated. Evoked eye movements were limited in amplitude to +/- 3-6 degrees, increasing with the size of the animal. Head movements were limited to +/- 30-40 degrees. Resetting fast-phases of both head and eyes were very rarely observed during sinusoidal stimulation and no eye movements were recorded in the absence of intended head movements. Vestibularly evoked head movements exhibited a frequency-dependent threshold that was not observed for vestibulo-ocular responses. Above threshold, the gain of evoked head responses increased and reached a frequency-dependent plateau at which the system behaved approximately linearly. Within the linear range, gain of vestibularly evoked responses increased with frequency (from 0.04 at 0.025 Hz to 0.75 at 0.5 Hz) and phase lead decreased (from about 80 degrees to 0 degrees). Vestibularly evoked eye movements similarly increased in gain from 0.05 to 0.56 and decreased in phase lead from about 56 degrees to 10 degrees over the same frequency range. Optokinetically evoked head and eye movements had their highest gains (about 0.8 and 0.5) at low constant velocities (less than or equal to 1-4 degrees/S) or frequencies (less than or equal to 0.025 Hz). At higher constant velocities or frequencies the gain dropped. The phase lag increased from close to zero (at 0.025 Hz) to about 60 degrees for the head and to about 20 degrees for the eye movements (at 0.25 Hz). These phase lags are explained by reaction times of the evoked movements of about 600 ms (head) and 200 ms (eyes). Combined stimulation evoked compensatory head movements with gain and phase values that were frequency-independent in the linear range. Head movements compensated for about 80-90% of the imposed gaze shift with a small phase lag (0-10 degrees). Evoked eye movements were found to be large enough in amplitude and fast enough in time to enable a frog to stabilize its gaze exclusively with slow phase compensatory movements for a large variety of frequency and amplitude combinations. The two motor systems controlling movements of the head and the eye are matched in such a way that the non-linearities of the evoked eye movements can compensate for the non-linearities of the evoked head movements.
将未受约束的青蛙记录的代偿性头部运动与头部固定的动物记录的代偿性眼球运动进行了比较。通过在黑暗中振荡动物(前庭刺激)、在固定于地面的有图案视觉背景前的光照下振荡动物(联合刺激)或围绕静止动物旋转垂直黑白条纹(视动刺激)来诱发运动。振荡发生在水平面上,频率在0.025至0.5赫兹之间。计算了头部和眼球运动相对于刺激运动的增益和相位值。诱发的眼球运动幅度限制在±3 - 6度,随动物大小增加。头部运动限制在±30 - 40度。在正弦刺激期间,极少观察到头部和眼球的快速复位相,并且在没有预期头部运动时未记录到眼球运动。前庭诱发的头部运动表现出频率依赖性阈值,这在前庭眼反射中未观察到。高于阈值时,诱发的头部反应增益增加并达到频率依赖性平台期,在此期间系统表现出近似线性。在线性范围内,前庭诱发反应的增益随频率增加(从0.025赫兹时的0.04增加到0.5赫兹时的0.75),相位超前减小(从约80度减小到0度)。在前庭诱发的眼球运动中,在相同频率范围内,增益同样从0.05增加到0.56,相位超前从约56度减小到10度。视动诱发的头部和眼球运动在低恒定速度(小于或等于1 - 4度/秒)或频率(小于或等于0.025赫兹)时具有最高增益(约0.8和0.5)。在较高恒定速度或频率时,增益下降。相位滞后从接近零(在0.025赫兹时)增加到头部约60度、眼球运动约20度(在0.25赫兹时)。这些相位滞后由诱发运动的反应时间约600毫秒(头部)和200毫秒(眼球)来解释。联合刺激诱发的代偿性头部运动在其线性范围内具有与频率无关的增益和相位值。头部运动补偿了约80 - 90%的施加的注视转移,相位滞后较小(0 - 10度)。发现诱发的眼球运动幅度足够大且时间足够快,以使青蛙能够通过慢相代偿性运动针对各种频率和幅度组合专门稳定其注视。控制头部和眼球运动的两个运动系统以这样一种方式匹配,即诱发眼球运动中的非线性可以补偿诱发头部运动中的非线性。