Schor C M
Am J Optom Physiol Opt. 1986 Aug;63(8):587-609.
The tonic resting level of accommodation, measured with an objective infrared optometer in an open-loop state (pinhole pupil or empty field), was increased by more than 1.75 D from baseline measures of resting focus after adapting monocularly for 1 min to a 2 D minus lens. The accommodative aftereffect disappeared in darkness, but returned when a visible stimulus reappeared in the open-loop state. Stimulation of disparity vergence with 10 delta, while accommodation was in an open-loop state, also increased the resting focus of accommodation. Similarly, the tonic resting level of vergence became more esophoric after adapting for less than 1 min to base-out prism or to a minus lens presented while the vergence loop was opened. The effects of tonic accommodation on accommodative vergence and the effects of tonic vergence on vergence accommodation were investigated with the temporal frequency responses of the AC/A and CA/C ratios to sinusoidal variations in blur (2 D) and disparity (10 delta), respectively. Accommodative vergence was unresponsive to low temporal frequency sinusoidal variations in blur (less than 0.1 Hz). Similarly, vergence accommodation was unresponsive to low temporal frequency sinusoidal variations in disparity. However, accommodative vergence and vergence accommodation were responsive to higher temporal frequency stimuli (up to 0.5 Hz). When negative feedback to the stimulated system (accommodation or vergence) was cancelled electronically, the low temporal frequency response increased for the AC/A and CA/C ratios, respectively. There was also a nonlinear increase of both AC/A and CA/C ratios as stimulus amplitude increased. It is hypothesized that the nonlinearity resulted from limitations of adaptation to small stimuli. An inverse complementary relation is suggested between the amplitude of the AC/A ratio and adaptable tonic accommodation, and between the amplitude of the CA/C ratio and adaptable tonic vergence. This model predicts that in this complementary relation, adaptable tonic elements would sustain motor responses of accommodation and vergence that were initiated by phasic elements and cross-link interactions. It also predicts that the AC/A and CA/C ratios would decrease in time as dynamic control shifted from the phasic to the adaptable tonic control mechanisms of accommodation and vergence, respectively.
在开环状态(针孔瞳孔或空白视野)下,使用客观红外验光仪测量的调节性静息水平,在单眼适应2D负透镜1分钟后,相较于静息焦点的基线测量值,增加了超过1.75D。调节后效在黑暗中消失,但当在开环状态下再次出现可见刺激时又会恢复。在调节处于开环状态时,用10棱镜度刺激视差性聚散,也会增加调节的静息焦点。同样,在聚散环打开的情况下,适应小于1分钟的外展棱镜或负透镜后,聚散的静息水平会变得更加内隐斜。分别通过AC/A和CA/C比率对模糊(2D)和视差(10棱镜度)的正弦变化的时间频率响应,研究了紧张性调节对调节性聚散的影响以及紧张性聚散对聚散性调节的影响。调节性聚散对低时间频率的模糊正弦变化(小于0.1Hz)无反应。同样,聚散性调节对低时间频率的视差正弦变化也无反应。然而,调节性聚散和聚散性调节对较高时间频率的刺激(高达0.5Hz)有反应。当对受刺激系统(调节或聚散)的负反馈通过电子方式消除时,AC/A和CA/C比率的低时间频率响应分别增加。随着刺激幅度的增加,AC/A和CA/C比率也呈非线性增加。据推测,这种非线性是由于对小刺激的适应限制所致。有人提出AC/A比率的幅度与可适应的紧张性调节之间、CA/C比率的幅度与可适应的紧张性聚散之间存在反向互补关系。该模型预测,在这种互补关系中,可适应的紧张性成分将维持由相位成分和交联相互作用引发的调节和聚散的运动反应。它还预测,随着动态控制分别从调节和聚散的相位控制机制转变为可适应的紧张性控制机制,AC/A和CA/C比率会随时间下降。