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患病眼睛中的时间整合。

Temporal integration in diseased eyes.

作者信息

Kono M, Yamade S

机构信息

Department of Ophthalmology, Shiga University of Medical Science, Japan.

出版信息

Int Ophthalmol. 1996;20(5):231-9. doi: 10.1007/BF00131917.

Abstract

We examined critical duration for visual acuity in eyes with central serous retinopathy (CSR), macular edema (ME) and glaucoma. Critical duration for visual acuity is the minimum period of time to perceive the acuity chart of his best. Visual acuity was measured at several limited exposure durations and the results were then compared with that of normal eyes. The acuity target was a single Landolt ring. The size, direction, and exposure duration of the target were computer controlled. The mean critical duration for visual acuity of the CSR and ME groups was 1.78 s and 2.69 s. These were significantly longer than that of the normal group (0.62 s). The critical duration of the glaucoma group was 0.42 s, which was not significantly prolonged. Critical duration for the increment or static threshold was measured for the purpose of comparison, and no significant differences were found between the diseased eyes (the CSR and ME groups) and the normal eyes, although the thresholds were significantly higher in the diseased eyes. Next, fixation movements which occurred during visual acuity testing were observed in order to investigate their role in acuity testing. In both normal and ME eyes the frequency and amplitude of microsaccades were smaller while the visual acity chart was shown. This suggests that microsaccades play no positive role in the reading of acuity charts, and that they bear little relation to the phenomenon of critical duration for visual acuity. From these results we hypothesized that in the CSR and ME groups the X-type ganglion cells send incomplete information to the central neural system. Thus, a longer time is required to obtain complete information before responding. Furthermore, one glaucoma case suggested that in diseased eyes in which mainly the Y-cell systems are damaged, temporal specificity in visual acuity for shorter exposure duration may reveal different response patterns.

摘要

我们研究了中心性浆液性视网膜病变(CSR)、黄斑水肿(ME)和青光眼患者眼睛的视力临界持续时间。视力临界持续时间是能够看清其最佳视力表的最短时间。在几个有限的暴露持续时间下测量视力,然后将结果与正常眼睛的结果进行比较。视力目标是单个兰道环。目标的大小、方向和暴露持续时间由计算机控制。CSR组和ME组的平均视力临界持续时间分别为1.78秒和2.69秒。这些时间明显长于正常组(0.62秒)。青光眼组的临界持续时间为0.42秒,没有显著延长。为了进行比较,测量了增量或静态阈值的临界持续时间,尽管患病眼睛(CSR组和ME组)的阈值明显更高,但患病眼睛和正常眼睛之间没有发现显著差异。接下来,观察视力测试期间发生的注视运动,以研究它们在视力测试中的作用。在显示视力表时,正常眼睛和ME眼睛的微扫视频率和幅度都较小。这表明微扫视在视力表阅读中没有起到积极作用,并且它们与视力临界持续时间现象几乎没有关系。从这些结果我们推测,在CSR组和ME组中,X型神经节细胞向中枢神经系统发送的信息不完整。因此,在做出反应之前需要更长的时间来获取完整信息。此外,一个青光眼病例表明,在主要Y细胞系统受损的患病眼睛中,较短暴露持续时间下视力的时间特异性可能会显示出不同的反应模式。

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