Amplitude-temporal characteristics of evoked responses of the visual analyzer to stimuli of growing intensity

A study was made on cats of the dependence of latency, peak latency, amplitudes and slopes of I and II phases of primary evoked potentials in the chiasm, the colliculi, the lateral geniculate body and visual cortex on the intensity of the photic stimulus in the range of intensities of II orders above the threshold. Practically in the whole examined range, the logarithmic connection is retained, testifying to the extremely wide possibility of the visual system to discriminate a signal in securing a reflex act.     

Cortical distribution of photic evoked potentials

Short-latency evoked potentials (EPs) of the primary response (PR) type, recorded to flashes over wide areas outside the visual cortex, reflect the true arrival of visual impulses in these areas and are not the result of the passive spread of the EPs over the brain tissue. The EPs do not disappear after extirpation of the visual cortex in "nonvisual" areas of the neocortex. They continue to arise also after division of the internal capsule sparing its posterior third. EPs are no longer recorded after division of the posterior third of the internal capsule. It is concluded from these results that the spread of impulses evoked by photic stimulation, not only into the visual areas, but also into other areas of the posterolateral thalamic nuclei.S. M. Kirov Medical Institute, Gor'kii. Translated from Neirofiziologiya, Vol. 2, No. 5, pp. 482–487, September–October, 1970.     

Statistical analysis of the parameters defining the cortical visual evoked potentials in the phases of the sleep-wake cycle

Visual evoked potential parameters (latencies, intervals of latencies and amplitudes) obtained by photic stimulation using a light-emitting diode implanted in the frontal sinus of cats were studied by statistical methods (analysis of variance) during the stages of wakefulness, slow sleep and paradoxical sleep. The results show: a) greater intraindividual homogeneity in all cases with special emphasis on the latencies; b) the greatest homogeneity of responses was found during slow sleep and paradoxical sleep stages; c) in relation to the influences exerted by the sleep-wakefulness cycle on the visual evoked potentials, the parameters most affected were those closely related to the secondary complex. We conclude, that latency, due to its great homogeneity, is the most useful parameter in this kind of experiments and secondly, that it is the secondary complex of the visual evoked potentials that is affected by the endogenous conditions of the subject (in our case the sleep-wakefulness cycle stage).     

Electrophysiological analysis of cortico-tectal connections in the turtle

Two types of evoked potentials are recorded in the tectum mesencephali in response to electrical stimulation of the forebrain surface of the turtleEmys orbicularis. The results of a layer-by-layer analysis show that evoked potentials of type I in response to stimulation of the hippocampal and piriform cortex are generated outside the tectum. Evoked potentials of type II, consisting of two surface-negative components, are recorded in the tectum in response to stimulation of the rostro-central surface of the forebrain. The first component appeared after a latent period of 20 msec and lasted 40–60 msec; the second component appeared after 80–100 msec and lasted 100–300 msec. Layer-by-layer and pharmacological analysis showed that the first component of the type II evoked potential is generated in the tegmental structures of the mesencephalon, whereas the second (long-latency) is generated in the tectum. The tectal origin of the second component is confirmed by its interaction with the tectal response to photic stimulation or to electrical stimulation of the optic nerve, evidence that these evoked potentials are generated by common structures. The efferent pathway from the dorsal cortex to the primary visual center is unilateral and has features of polysynaptic projections (long latent period, low lability).     

Mechanisms of interaction between the parietal association and projection areas of the cat neocortex

Changes in evoked potentials in the first visual (VI), first somatic (SI), and parietal areas of the cortex during local cooling of each area were investigated under pentobarbital anesthesia. Two types of interaction were distinguished. Type I interaction was found in all areas in the early stages of local cooling and was reflected in a similar decrease in amplitude of evoked potentials in intact parts of the cortex. In the thalamic association nuclei — the pulvinar and posterolateral nucleus — somatic evoked potentials were unchanged but visual were transformed differently from those in the cortex. Type IIinteraction was found in the later stages of cooling and only between the association area and each of the projection areas. It was reflected in a greater change in amplitude of the evoked potentials and also in their configuration. In response to somatic stimulation in the early stage of type II interaction transformation of evoked potentials in the cortex took place sooner than in the nuclei; in the later stage it took place immediately after transformation of the "subcortical" evoked potentials. In response to photic stimulation transformations of cortical evoked potentials were always preceded by the corresponding transformations in the nuclei. It is suggested that type I interaction is formed by intercortical connections and type II by direct and subcortical relay connections. Differences in the role of the association area in interaction of types I and II when activated by stimuli of different modalities are discussed.Brain Institute, Academy of Medical Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 10, No. 6, pp. 573–581, November–December, 1978.     

An analysis of interhemispheric interrelationships in the visual cortex of cats based on the law of contrast perception of light]

The dependence of EP amplitude on the intensity of photic stimuli before and after section of the callosal body may be fully defined by the equation of the contrast law of light perception. Analysis of the nature of interhemispheric relationships by means of contrast law has shown that both reciprocal depressing and reciprocal facilitating interhemispheric relationships may exist in the primary visual cortical projection zone, and reciprocal facilitating interhemispheric influences in the secondary visual projection zone. Similarity of interhemispheric relationships has been recorded in the primary visual cortex in cats and in the secondary one, in rats, as well as in the socondary visual cortical zone in cats, and in the primary, in rats. Interhemispheric reciprocal influences in the whole range of stimuli intensities are distributed more uniformly in cats than in rats. Cats may perceive a wider range of intensity of photic stimuli than rats. In cats as in rats, the effectiveness of processing of the photic stimuli contrast is greater in the secondary visual cortical projection zone than in the primary one.     

视力与视觉诱发电位的相关分析

对104例病人的图形翻转VEP的瞬态波形各参数,以及9例正常或近视学生的稳态曲线功率谱与视力之间的关系进行了多元相关统计分析,旨在探讨VEP的哪些参数可客观地评估视力.结果表明,瞬态VEP的波形参数中以13’格诱发的N_1P_1、P_1N_2的峰峰值及P_(100)潜伏期与视力的相关系数最大,故认为,分析视力时以平均P_(100)波的波幅值和P_(100)波潜伏期作指标较为灵敏;而稳态、VEP能谱曲线则显示,视力与平均相叶能谱或刺激频率点的能谱相关性较大,与二次谐波的相关性则小.     

The effect of M-cholinolytics on the lability of rabbit visual analyzer structures]

The influence of M-cholinolytics (amizyl, glipine, cyclozyl and 4-oxypiperidylbenzylate) in 0.01--10 mg/kg doses on EEG and photic driving in structures of the visual analyser was studied in experiments on twenty intact rabbits with chronically implanted electrodes in the optic chiasm, the optic tract, the lateral geniculate body and the visual cortex. All M-cholinolitics in the doses studied produced synchronization of the EEG. Photic stimulation against the background of small doses of M-cholinolytics (0.01--0.5 mg/kg) did not lead to any disturbances of photic driving. With increased doses of cholinolitics up to 1--5 mg/kg only low frequencies (1--5 imp/sec) produced driving in the lateral geniculate body and the visual cortex, while in the optic tract the driving remained at the initial level. Administration of drugs in a 10 mg/kg dose resulted in complete depression of the driving response in the lateral geniculate body and visual cortex, while in the optic tract the driving was retained.     

Cortical visual evoked potentials during the sleep wakefulness cycle of the freely moving cat. Characterization and statistical comparisons

Visual evoked potentiels (VEPs) were obtained during the stages of wakefulness (W), slow sleep (SS) and paradoxical sleep (PS) by means of a light-emitting diode chronically implanted in the frontal sinus of the freely moving cat. Statistical analysis of the variables: latencies, latency intervals and amplitudes, between each of the mentioned stages shows that, for the first components, variations occurred only in the first interval of latency during SS vs. W. Lengthening of VEP latencies and increase of VEP amplitudes were observed for all secondary components in the comparisons between both SS and W, and SS and PS. PS-VEPs vs. W-VEPs showed shortening of latencies and decrease of amplitudes of all secondary components of the former case. The results confirm that in the freely moving cat, the secondary VEP response is more intensely affected by sleep than the primary VEP response, but indicate that there are different mechanisms in the generation of the VEP during SS and PS.     

Two photic pathways contribute to pineal evoked responses

In this study, average photic evoked responses were recorded simultaneously in freely behaving rats from the pineal body and the ventromedial hypothalamus; permanent semimicroelectrodes were implanted several days before the experiments were begun, and both local anesthesia (xylocaine), sympathectomy, and general anesthesia (barbiturate) were used as tools to find out whether or not photic responses are transmitted to the pineal via the superior cervical ganglion (scg)-nervi conorii and/or through another CNS route. The experiments demonstrated that the photic evoked responses recorded from the pineal are transmitted via two separate routes: one, a fast pathway with a “shorter” latency, via the CNS, i.e., the habencular posterior commissure complex, and the other a “slower” (or longer) pathway via the scg to the pineal.     

The effect of selective attention on pattern-specific visual evoked potentials

In a complex choice reaction time experiment, patterned stimuli without luminance change were presented, and pattern-specific visual evoked potentials to lower half-field stimulation were recorded. Two experimental conditions were used. The first was the between-field selection, where square patterns were presented in either the lower or the upper half of the visual field. In a given stimulus run one of the half-fields was task-relevant, and the subjects' task was to press a microswitch to stimuli of higher duration value (GO stimuli), while they had to ignore shorter ones, i. e. stimuli of lower apparent spatial contrast (NOGO stimuli). They had to ignore the stimuli appearing in the irrelevant half-field (IRR stimuli). In order to ensure proper fixation, the subjects had to press another microswitch at the onset of a dim light at the fixation point (CRT stimuli). Our second experimental condition was the within-field selection, where the GO, NOGO, and IRR stimuli appeared in the lower half of the visual field. GO and NOGO were square patterns while IRR stimuli were constructed of circles, or vice versa. (The CRT stimuli were the same as in the previous condition.) Three pattern-specific visual evoked potential components were identified, i. e. CI (70 ms latency), CII (100 ms latency), and CIII (170 ms latency). There were marked selective attention effects on both the CI-CII and CII-CIII peak-to-peak amplitudes. In both experimental conditions, responses with the highest amplitude were evoked by the GO type of stimuli, while the IRR stimuli evoked the smallest responses. According to these results, attention effects on the pattern-specific visual evoked potentials in the first 200 ms cannot be attributed to a simple stimulus set kind of selection.     

Electrical potentials from the eye and optic nerve of Strombus: effects of electrical stimulation of the optic nerve.

1. Photic stimulation of the mature eye of Strombus can evoke in the optic nerve 'on' activity in numerous small afferent fibres and repetitive 'off' bursts of afferent impulses in a smaller number of larger fibres. 2. Synchronous invasion of the eye by electrically evoked impulses in small optic nerve fibres (apparently the 'on' afferents, antidromically activated) can evoke a burst of impulses in the larger 'off' fibres which propagate away from the eye. Invasion of the eye via one branch of optic nerve can evoke an answering burst in another branch. 3. Such electrically evoked bursts are similar to light-evoked 'off' bursts with respect to their impulse composition, their ability to be inhibited by illumination of the eye, and their susceptibility to MgCl2 anaesthesia. 4. Invasion of the eye by a train of repetitive electrically evoked impulses in the absence of photic stimulation can give rise to repetitive 'off' bursts as well as concomitant oscillatory potentials in the eye which are similar to those normally evoked by cessation of a photic stimulus. 5. The electrically evoked 'off' bursts appear to be caused by an excitatory rebound following the cessation of inhibitory synaptic input from photoreceptors which can be antidromically activated by electrical stimulation of the optic nerve. 6. The experimental results suggest that the rhythmic discharge of the 'off' fibres evoked by the cessation of a photic stimulus is mediated by the abrupt decrease of inhibitory synaptic input from the receptors.     

Effects of timing of inspiratory occlusion on cerebral evoked potentials in humans

Previous studies from these laboratories have shown that airway occlusion applied from the onset of inspiration or during midinspiration is associated with cerebral evoked potentials in human subjects. The hypothesis tested in the present study was that the more abrupt decrease in mouth pressure produced by midinspiratory occlusion will be associated with evoked potentials that have shorter peak latencies and greater peak amplitudes than those produced by occlusions from the onset of inspiration. The second objective of the present study was to determine whether there is bilateral projection of inputs from the respiratory system to the somatosensory cortex. Random presentation of 64 midinspiratory occlusions and 64 occlusions from the onset of inspiration was performed in eight subjects. The inspirations preceding the occlusions served as control. Evoked potentials were recorded from the scalp with electrode pairs Cz-C3 and Cz-C4. Reaction time to each type of occlusion was measured from the burst in electromyogram activity produced by contraction of the muscles encircling the eye. Each type of inspiratory occlusion was associated with evoked potentials that could be recorded bilaterally. The peak amplitudes of the evoked potentials recorded over the right cerebral hemisphere were significantly greater than those recorded from the left side. The peak amplitude was greater and the peak latency shorter for the evoked potentials produced by the midinspiratory occlusions. The results are consistent with the hypothesis that afferents mediating these potentials are stimulated by added loads to breathing and project bilaterally to the somatosensory cortex in humans.     

Hemispheric asymetry of the evoked electrical activity of the cerebral cortex to letter and non-verbal stimuli]

Average evoked potentials (AEP) were recorded in practically healthy subjects to "meaningless" figures and letters, presented to different halves of the visual field. Analysis of the amplitudes of AEP late components to verbal and non-verbal stimuli reveals hemispheric asymmetry. A higher amplitude of the late positive evoked response (P300) to a "direct" stimulation both by verbal and non-verbal stimuli (in the contralateral field of vision) is recorded in the left hemisphere than in the right one. Similar stimulation of the right hemisphere does not reveal sucha difference. In the left hemisphere the P300 wave is of a clearly greater amplitude to a "direct" stimulation (contralateral visual field) than to an "indirect" one (ipsilateral visual field), regardless of the nature of the stimulus. No such difference is observed in the right hemisphere. The magnitude of the late negative wave (component N200) to non-verbal stimuli is greater in the right hemisphere both in response to "direct" and "indirect" stimulations. No intrahemispheric difference has been found in the amplitude of late evoked responses of the cerebral cortex to verbal and non-verbal stimuli.     

Physiological response properties of cat retinal ganglion cells projecting to suprachiasmatic nucleus

The aim of this experiment was to characterize the physiological properties of cat retinal ganglion cells that project to the suprachiasmatic nucleus (SCN). Retrogradely labeled SCN-projecting ganglion cells were recorded extracellularly in vitro. For the first time, this study provides crucial information on visual response properties of ganglion cells in the entrainment circuitry. All recorded cells gave sustained responses (n = 9). Although most of the cells (n = 8) had an "on" center receptive field, one cell showed "on-off" center receptive field properties. The range of receptive field sizes was 2 to 5 deg. For most of the cells tested, the spectral wavelength that evoked peak responses was 500 nm (3 out of 5 cells). All recorded cells (n = 9) preferred still or extremely slow-moving stimuli (3.3 deg/s). These results indicate that cat SCN-projecting cells receive inputs from conventional photoreceptors. The hypothesis that both conventional and cryptochromic photoreceptors are involved in transferring photic signals is discussed.     

When the Sun Prickles Your Nose: An EEG Study Identifying Neural Bases of Photic Sneezing

Background

Exposure to bright light such as sunlight elicits a sneeze or prickling sensation in about one of every four individuals. This study presents the first scientific examination of this phenomenon, called ‘the photic sneeze reflex’.

Methodology and Principal Findings

In the present experiment, ‘photic sneezers’ and controls were exposed to a standard checkerboard stimulus (block 1) and bright flashing lights (block 2) while their EEG (electro-encephalogram) was recorded. Remarkably, we found a generally enhanced excitability of the visual cortex (mainly in the cuneus) to visual stimuli in ‘photic sneezers’ compared with control subjects. In addition, a stronger prickling sensation in the nose of photic sneezers was found to be associated with activation in the insula and stronger activation in the secondary somatosensory cortex.

Conclusion

We propose that the photic sneeze phenomenon might be the consequence of higher sensitivity to visual stimuli in the visual cortex and of co-activation of somatosensory areas. The ‘photic sneeze reflex’ is therefore not a classical reflex that occurs only at a brainstem or spinal cord level but, in stark contrast to many theories, involves also specific cortical areas.     

Phase relationships of cortical potentials in rabbits in different functional states

Phase shifts in EEG potentials were investigated in the rabbit cortex during photic stimulation and in controls. Degree of phase shift in the predominating theta waves was found to increase gradually with increasing distance between recording electrodes both with and without photic stimulation, pointing to the existence of a phase gradient — the conditions appropriate to the greater proportion of motor reactions. Photic stimulation induces an increase in numbers of non-phasic EEG waves recorded from close-lying sites as well as reduced scatter in levels of phase shift between EEG of the sensorimotor and visual cortex, thus rendering phase shifts more stable. Irradiation of excitation from the visual to the motor analyzer in response to photic stimulation occurs against a background of high correlation coefficient and coherent function levels and with a phase shift from 0 to 10–11°.Institute of Higher Nervous Activity and Neurophysiology, Academy of Sciences of the USSR. Moscow. Translated from Neirofiziologiya, Vol. 21, No. 4, pp. 507–513, July–August, 1989.     

Trace reactions following combination of a sensory stimulus with polarization of the visual region of the cortex]

Spontaneous activity and responses to photic flashes and tones of 133 neurones were recorded in the visual cortex during polarization of the same area (1.5 to 10 muA, 5 to 30 min) and after it (one to 52 min). Responses of cells to two unimodal stimuli of different parameters were analysed, of which one was presented repeatedly during the polarization ("positive"), and the other one to three times ("negative"). Depending on the previous "learning", 47.4% of the units responded after the polarization to "positive" photic stimulus and 37,8%--to acoustic stimulus. The trace effects of the stimuli pairings are reproduced in polarization after-effect by the action of the sensory signal alone. The recorded differences in the nature and duration of the reproduction of trace processes formed to an adequate and inadequate stimuli, are due to the dissimilar action of polarizing currents on neurones of the cortex cross-section and to different effectivity of the visual and non-visual influences related to it.     

Visual evoked potentials and event related potentials in congenitally deaf subjects

The purpose was to test parameters of visual evoked potentials (VEPs) and of event-related potentials (ERPs) in deaf subjects to verify visual and cognitive CNS functions in a handicapped group of the population. Three types of visual stimuli (with dominating parvocellular or magnocellular system activation or with cognitive tasks) were used in the study. Six deaf persons (4 women, 2 men, mean age 17 years) and 6 persons with normal hearing (sex- and age-matched) were included in this pilot study. In all types of stimulation, latencies and amplitudes of main VEPs and ERPs components were evaluated. No significant latency differences were found. However, significantly reduced amplitudes were found in the occipital area for responses to motion and cognitive stimuli which might be interpreted as a part of functional reorganization of the extrastriate and cognitive cortical areas of deaf subjects.