图形视网膜电图研究的新进展

图形视网膜电图(PERG)是视网膜的综合电反应,是用亮度呈周期变化的光栅或周期翻转的黑白相间的图形诱发。其幅度是图形的空间频率和时间频率的函数,也受图形的对比度及清晰度影响。基础和临床研究都提示PERG可能起源于神经节细胞。一旦神经节细胞的活动发生异常,PERG明显减小或消失。PERG为人的视网膜细胞活动的分层分析提供了一种有效的手段,具有广泛的应用前景。     

用显示器测量办公亮度环境下的人眼对比度敏感视觉特性

对比度敏感是描述人眼视觉系统空间特性的主要指标之一,对比度敏感函数是反映不同条件下的对比度敏感与空间频率之间的关系。人眼对比度敏感数据的测量受到环境亮度较大的影响,为了研究常用办公环境条件下的人眼对比度敏感情况,对6位青年在环境亮度分别为153,312,470 cd/m2和暗室条件下,在距离为2米处观测11种空间频率的矩形光栅进行测量,光栅用显示器进行显示,其平均亮度分别为60和90 cd/m2。实验结果表明,对于相同频率的光栅,人眼对比度敏感程度随着环境亮度的增加而减小,而且人眼在暗室环境下比在办公环境条件下对亮度光栅更敏感;但是在观测平均亮度为60cd/m2的光栅时,人眼特殊地对在环境亮度为312 cd/m2的条件下更敏感。     

用显示器测量办公亮度环境下的人眼对比度敏感视觉特性

对比度敏感是描述人眼视觉系统空间特性的主要指标之一,对比度敏感函数是反映不同条件下的对比度敏感与空间频率之间的关系。人眼对比度敏感数据的测量受到环境亮度较大的影响,为了研究常用办公环境条件下的人眼对比度敏感情况,对6位青年在环境亮度分别为153,312,470 cd/m2和暗室条件下,在距离为2米处观测11种空间频率的矩形光栅进行测量,光栅用显示器进行显示,其平均亮度分别为60和90 cd/m2。实验结果表明,对于相同频率的光栅,人眼对比度敏感程度随着环境亮度的增加而减小,而且人眼在暗室环境下比在办公环境条件下对亮度光栅更敏感;但是在观测平均亮度为60cd/m2的光栅时,人眼特殊地对在环境亮度为312 cd/m2的条件下更敏感。     

双眼和单眼视觉剥夺猫外膝体细胞的图形适应

为测定丘脑外膝体细胞的图形适应是否依赖于早期视觉经验,在细胞外记录了双眼和单眼缝合的猫外膝体中断细胞对手工时间运动光栅刺激的反应。在双眼剥夺猫,占６８％的记录到的细胞在３０ｓ内反应下降到稳定值,其平均反应值下降３３％,适应程度较正常猫显著。在单眼剥夺猫,记录到的剥夺眼驱动的和非剥夺眼驱动的细胞中,分别有占５３％和４４％的细胞显示图形适应,两者差别不大。研究表明,早期视剥夺能增强或保持图形适应,提示     

瞳孔控制系统非线性的频率特性与固有频率

本文用实验方法从时域和频域上揭示了瞳孔对光反应的非线性特性.在亮度以正弦变化的光刺激下,瞳孔反应波形呈同步倍频现象;描述函数的频率-振幅特性曲线呈多峰的锯齿形;具有1.2Hz左右的系统固有频率和极限环现象.     

华虻小叶神经元运动敏感性的研究

用电生理细胞内记录的方法记录了１０个以上小叶神经元对闪光、运动光斑及运动光栅刺激的电生理反应特点,结果表明：（１）小叶神经元对闪光刺激具有特征性反应,细胞对给光和撤光刺激都会表现出不同程度的去极化和超极化,反应的波形不随闪光时间的改变而改变,两次去极化之间的时间间隔与闪光刺激的时间长度成线性关系;（２）小叶神经元对运动光斑的运动速度非常敏感,而对光斑的运动方向的改变却不敏感,尽管有的细胞存在一个能使反应的变化更快的优势方向,但并没有明显的运动方向选择性;（３）小叶神经元对运动光栅的响应频率受光栅的空间频率和运动速度的双重调制,与光栅的运动方向无关。     

综述: 初级视皮层的亮度信息加工

亮度(luminance)是最基本的视觉信息.与其他视觉特征相比,由于视神经元对亮度刺激的反应较弱,并且许多神经元对均匀亮度无反应,对亮度信息编码的神经机制知之甚少.初级视皮层部分神经元对亮度的反应要慢于对比度反应,被认为是由边界对比度诱导的亮度知觉(brightness)的神经基础.我们的研究表明,初级视皮层许多神经元的亮度反应要快于对比度反应,并且这些神经元偏好低的空间频率、高的时间频率和高的运动速度,提示皮层下具有低空间频率和高运动速度通路的信息输入对产生初级视皮层神经元的亮度反应有贡献.已经知道初级视皮层神经元对空间频率反应的时间过程是从低空间频率到高空间频率,我们发现的早期亮度反应是对极低空间频率的反应,与这一时间过程是一致的,是这一从粗到细的视觉信息加工过程的第一步,揭示了处理最早的粗的视觉信息的神经基础.另外,初级视皮层含有偏好亮度下降和高运动速度的神经元,这群神经元的活动有助于在光照差的环境中检测高速运动的低亮度物体.     

猫外膝体神经元对光栅刺激方位倾向性的一种分布特性

我们检测了猫外膝体(LGN)神经元对闪烁方波光栅的反应与光栅方位的关系。对一定对比度和空间频率的光栅,26个记录到的神经元的反应均随方位不同而变化,其最大反应和最小反应的比值平均为3.0±0.3(S.E.)。神经元的最优方位(即引起最大反应的光栅方位)随其感受野中心在视网膜上的位置而异,具有平行于其各自感受野中心与视网膜中央区(area cen-sralis)的连接线的倾向。     

初级视皮层的亮度信息加工

亮度(luminance)是最基本的视觉信息.与其他视觉特征相比,由于视神经元对亮度刺激的反应较弱,并且许多神经元对均匀亮度无反应,对亮度信息编码的神经机制知之甚少.初级视皮层部分神经元对亮度的反应要慢于对比度反应,被认为是由边界对比度诱导的亮度知觉(brightness)的神经基础.我们的研究表明,初级视皮层许多神经元的亮度反应要快于对比度反应,并且这些神经元偏好低的空间频率、高的时间频率和高的运动速度,提示皮层下具有低空间频率和高运动速度通路的信息输入对产生初级视皮层神经元的亮度反应有贡献.已经知道初级视皮层神经元对空间频率反应的时间过程是从低空间频率到高空间频率,我们发现的早期亮度反应是对极低空间频率的反应,与这一时间过程是一致的,是这一从粗到细的视觉信息加工过程的第一步,揭示了处理最早的粗的视觉信息的神经基础.另外,初级视皮层含有偏好亮度下降和高运动速度的神经元,这群神经元的活动有助于在光照差的环境中检测高速运动的低亮度物体.     

不同年龄组立体视及图形诱发电位的对比研究

由微机产生动态随机点立体图(DRDS)和黑白棋盘格图形刺激 ,记录了30名立体视觉正常的成人、30名学龄儿童和30名学龄前儿童的动态立体视诱发电位 (DDEP)和双眼棋盘格图形刺激的诱发电位(PVEP)。实验结果表明 ,三组动态立体视诱发电位的N波潜伏时有显著差异 ,随着年龄的增长 ,N波潜伏时缩短 ;而棋盘格刺激的视觉诱发电位的P100波的潜伏时无显著性差异 ,但波幅有显著差异 ,学龄儿童的波幅最高 ,成人的波幅最低。由DEP在各个年龄组的演变规律与棋盘格图形VEP的演变规律的不一致揭示了视觉系统中立体视发育和类似于棋盘格刺激的较为初级的视功能发育是不同步的 ,它们具有不同的发育规律 ;12岁以下儿童立体视仍具有可塑性。     

光点位移运动激发的瞬态瞳孔反应

用等高度的光点位移运动作为刺激来测量瞳孔反应,实验记录表明,即使输入到视网膜的总光通量不变,仅仅是刺激点的位置改变就能激发起瞳孔反应,且其反应的位置分辨率可达１０’,这一实检结果揭示了瞳孔对光反射通路不仅传递了进入瞳孔的总光通量的信息,而且还检测了刺激光点位置变化的信息。     

The Pupillary Light Response Reveals the Focus of Covert Visual Attention

The pupillary light response is often assumed to be a reflex that is not susceptible to cognitive influences. In line with recent converging evidence, we show that this reflexive view is incomplete, and that the pupillary light response is modulated by covert visual attention: Covertly attending to a bright area causes a pupillary constriction, relative to attending to a dark area under identical visual input. This attention-related modulation of the pupillary light response predicts cuing effects in behavior, and can be used as an index of how strongly participants attend to a particular location. Therefore, we suggest that pupil size may offer a new way to continuously track the focus of covert visual attention, without requiring a manual response from the participant. The theoretical implication of this finding is that the pupillary light response is neither fully reflexive, nor under complete voluntary control, but is instead best characterized as a stereotyped response to a voluntarily selected target. In this sense, the pupillary light response is similar to saccadic and smooth pursuit eye movements. Together, eye movements and the pupillary light response maximize visual acuity, stabilize visual input, and selectively filter visual information as it enters the eye.     

Contrast transfer function of the visual system]

Visually evoked potentials were used to determine the spatial contrast response function of the visual system and the visual acuity of the pigeon. The spatial contrast response describes the relationship between the contrast in a pattern of vertical stripes, whose luminance is a function of position, and the amplitude of the visually evoked response at various spatial frequencies for a given temporal frequency (pattern reversal frequency); it indicates how particular spatial frequencies are attenuated in the visual system. The visually evoked responses were recorded using monopolar stainless steel electrodes inserted into the stratum griseum superficiale of the optic tectum; the depth of penetration was determined on the basis of a stereotactic atlas. The stimulus patterns were generated on a video monitor placed 75 cm in front of the animal's eye perpendicular to the optic axis. The spatial contrast response function measured at 10% contrast and 0.5 Hz reversal frequency shows a peak at a spatial frequency of 0.5 c/deg, corresponding to 1 degree of visual angle, and decreases progressively at higher spatial frequencies. The high-frequency limit (cut-off frequency) for resolution of sinusoidal gratings, estimated from the contrast response function, is 15.5 c/deg, corresponding to a visual acuity of 1.9 min of arc.     

Development of contrast sensitivity and acuity of the infant colour system

We have monitored the development of infant colour vision by measuring chromatic contrast sensitivity and acuity in eight young infants over a period of 6 months. Steady-state visual evoked potentials (VEPS) were recorded in response to both chromatic (red-green) and luminance (red-black or green-black) patterns that were reversed in contrast over time. For most infants, no response could be obtained to chromatic stimuli of any size or contrast before 5 weeks of age, although luminance stimuli of 20% contrast gave reliable responses at that age. When responses to chromatic stimuli first appeared, they could be obtained only with stimuli of very low spatial frequency, 20 times lower than the acuity for luminance stimuli. Both contrast sensitivity and acuity for chromatic stimuli increased steadily, more rapidly than for luminance stimuli. As the spectral selectivities of infant cones are similar to those of adults, the difference in rate of development of luminance and chromatic contrast sensitivity and acuity stimuli probably reflects neural development of the infant colour system.     

Visual acuity of the midland banded water snake estimated from evoked telencephalic potentials

The visual acuity of seven midland banded water snakes was measured by recording evoked responses from telencephalon to temporally modulated square wave grating patterns. Using conventional electrophysiological techniques and signal averaging, high contrast square wave gratings of different spatial frequencies were presented. Acuity was estimated by extrapolating relative response amplitude/log₁₀ spatial frequency functions which yielded an average acuity of 4.25 cycles/degree. Refractive state was also estimated by recording evoked potentials to intermediate spatial frequencies with different lenses in front of the eye. Polynomial fits indicated that under the experimental conditions the snakes were around 6.4 diopters hyperopic suggesting a corrected acuity of 4.89 cycles/degree. Reduction of grating luminance resulted in a reduction in evoked potential acuity measurements. These results indicate that the spatial resolution of midland banded water snakes is the equal of cat; about 20/120 in human clinical terms.     

Neural adjustments to chromatic blur

The perception of blur in images can be strongly affected by prior adaptation to blurry images or by spatial induction from blurred surrounds. These contextual effects may play a role in calibrating visual responses for the spatial structure of luminance variations in images. We asked whether similar adjustments might also calibrate the visual system for spatial variations in color. Observers adjusted the amplitude spectra of luminance or chromatic images until they appeared correctly focused, and repeated these measurements either before or after adaptation to blurred or sharpened images or in the presence of blurred or sharpened surrounds. Prior adaptation induced large and distinct changes in perceived focus for both luminance and chromatic patterns, suggesting that luminance and chromatic mechanisms are both able to adjust to changes in the level of blur. However, judgments of focus were more variable for color, and unlike luminance there was little effect of surrounding spatial context on perceived blur. In additional measurements we explored the effects of adaptation on threshold contrast sensitivity for luminance and color. Adaptation to filtered noise with a 1/f spectrum characteristic of natural images strongly and selectively elevated thresholds at low spatial frequencies for both luminance and color, thus transforming the chromatic contrast sensitivity function from lowpass to nearly bandpass. These threshold changes were found to reflect interactions between different spatial scales that bias sensitivity against the lowest spatial grain in the image, and may reflect adaptation to different stimulus attributes than the attributes underlying judgments of image focus. Our results suggest that spatial sensitivity for variations in color can be strongly shaped by adaptation to the spatial structure of the stimulus, but point to dissociations in these visual adjustments both between luminance and color and different measures of spatial sensitivity.     

在双脉冲光刺激下瞳孔系统的采样控制特性

本文用实验揭示了瞳孔对光动态反应具有采样控制特性。实验中采用各种不同时间间隔的双脉冲光,以开环的方式(Maxwellian View)刺激瞳孔,当双脉冲之间间隔较长时,瞳孔反应相当于对双脉冲光的两次脉冲分别产生瞬态收缩;当双脉冲时间间隔短于0.6s 时,其反应就成了一次瞬态收缩,与单个光脉冲所引起的瞳孔反应一样。同—受试者的多次实验结果相同,不同受试者所得结果也基本一致。故瞳孔对脉冲刺激光引起反应后,必须至少约隔0.6s 才能对另一次脉冲光产生反应,这就说明了瞳孔动态反应具有离散的采样控制特性。实验还进一步证明,瞳孔系统的控制机制是双重模式的控制:不同的刺激条件下,瞳孔反应可呈现为瞬态反应(AC)或持续反应(DC),瞬态反应的 AC 通道为离散的采样控制,持续反应的 DC 通道为连续控制。     

瞳孔控制系统采样特性的中枢机制

本文以双脉冲光分眼刺激（ｄｉｃｈｏｐｔｉｃ ｓｔｉｍｕｌａｔｉｎｇ,双脉冲的第一脉冲光刺激一侧眼,第二脉冲光刺激另一侧眼）进行瞳孔采样特性研究。实验结果表明：当双脉冲之间的时间间隔较长时,瞳孔产生两次收缩反应;当时间间隔小于约０．６ｓ时,瞳孔只对第一个脉冲光刺激产生瞬态收缩,对第二个脉冲光刺激不产生反应。这不仅证实了单眼实验研究的结论：瞳孔系统不是在时间上连续进行控制,而是离散的采样控制,它对光刺     

Correlations Between Acetylcholinesterase Activity in Guinea-Pig Iris and Pupillary Function: A Biochemical and Pupillographic Study

: Acetylcholinesterase (AChE) in guinea pig iris was inhibited by methylisocyclopentylfluorophosphate (soman) administered topically or parenterally, and enzyme activity was correlated to pupillary diameter by infrared pupillography. After a single topical soman instillation into the conjunctival sac there was an almost linear relationship between the reduction in AChE activity and pupillary diameter. Topical administration of soman at 24-h intervals in doses capable of almost complete inhibition of AChE in iris was accompanied by a reduced miotic effect of this drug. This was indicated by a reduced rate of the soman-induced pupillary constriction, a less pronounced reduction in pupillary diameter, and a more rapid return of the pupillary diameter to normal size. The change in pupillary diameter occurred after three daily administrations and remained constant during 31 days of treatment. These observations were seen irrespective of inhibition of blood AChE. The decrease in response to repeated administration could not be explained by a reduced inhibitory effect of soman on AChE, by a more rapid de novo synthesis of AChE, or by a change in the number of the muscarinic receptors as determined by quinuclidinyl benzilate binding. When soman or DFP was administered subcutaneously in high doses a severe AChE inhibition was obtained in iris without any concomitant miosis.