Localization of the optic tract by using subcortical visual evoked potentials (VEPs) in cats.

OBJECTIVES: This study was aimed to clarify the relationship between the amplitudes of visual evoked near field potentials and distance from the optic tract, and to determine the adequate filter settings to record these potentials from the optic tract separately from the far field potentials. METHODS: The visual evoked near field potentials from the optic tract were consecutively recorded through intracerebral electrodes in 6 cats' brains. Different filter settings were tried and the amplitudes of visual evoked potentials (VEPs) were compared with the distance from the optic tract. RESULTS: The filter settings of 100 Hz to 1 kHz were the best to obtain only the near field potentials separately from the far field potentials. Histological sections revealed that the potentials of the surface of the optic tract showed sudden increase of amplitude, above the 50% of the maximum VEPs amplitudes. CONCLUSIONS: The optic tract can be identified using these methods. These results can be applied to localize the optic tract during such an operative procedure as postero-ventral pallidotomy.     

Visual wulst influences on flash evoked responses in the ectostriatum of the zebra finch

Anatomical data suggest that visual information from the thalamofugal pathway contributes to visual processing in the tectofugal pathway. We addressed the question of the functionality of anatomically described connections to the visual system of a laterally eyed bird, the zebra finch. The study shows the contribution of visual wulst efferents to visual processing in the ectostriatum by recordings of visually evoked slow field potentials. Suppression of visual wulst activity resulted in a selective reduction of distinct potential components in contralaterally evoked slow field potentials. A clear reduction was observed in the maximum amplitude of short latency components in the negative wave. Long latency components of the negative wave and the entire positive wave of the contralaterally flash evoked potentials were almost abolished. Ipsilateral visual evoked potentials (VEPs) were not significantly affected. Cooling and spreading depression of the optic tectum resulted in a uniform amplitude reduction of the negative wave. The positive wave was almost abolished. Ipsilateral VEPs disappeared completely during suppression of optic tectum activity. The results showed that the visual wulst has a significant, most likely facilitatory, influence on the processing of contralateral visual information in the ectostriatum. Ipsilateral stimulus processing was partly independent from visual wulst activity. A model for thalamo- and tectofugal connectivity in the ectostriatum is suggested.     

Do visual evoked potentials give relevant information to the neuro-ophthalmological examination in optic nerve lesions?

The visual evoked potentials (VEPs) and neuro-ophthalmological examinations of 134 patients were compared. The VEPs were abnormal in 95 % of the eyes with optic neuritis. Defective color vision was found in 99 %, visual field defects in 88 %, decreased vision in 66 % and an afferent pupillary defect in 55 %. 29 patients with optic neuritis were followed up with repeated tests. VEPs and color vision recovered more slowly than visual acuity and visual field.
Abnormal VEPs were observed in 68 % of 50 MS patients. An analysis of symptomatic and asymptomatic eyes showed that testing of color vision, visual field and red-free ophthalmoscopy were equally as useful diagnostic tools as VEPs. 4 (8 %) of the MS patients had abnormal VEPs despite a normal neuro-ophthalmological examination; 94 % of MS patients with symptoms and 47 % of MS patients without visual symptoms had abnormal VEPs.
VEPs were pathological in 59 % of 24 patients with traumatic or compressive optic nerve diseases or optic atrophies of unknown etiology. The neuro-ophthalmological examination was more sensitive than VEPs in the diagnosis of these disorders. A neuro-ophthalmological examination is in most cases sufficient to diagnose optic nerve lesions. VEPs are of diagnostic aid especially in mild optic nerve lesions.     

Identification of the trochlear motoneurons by retrograde transport of horseradish peroxidase

A common technique for demonstrating projections in the brain is to electrically stimulate one part of the brain and record mass or field potentials from another part. We showed in the visual system of the cat, where connections between retina, lateral geniculate nucleus, and superior colliculus are very well known, that the recording of field potentials is not at all sufficient to demonstrate connections. The most prominent potential after electrical stimulation of the optic tract is the field potential created by the Y-ganglion cell fibers of the optic nerve. We recorded this potential in the optic nerve head of the eye, in the lateral geniculate nucleus, and in the superior colliculus. To our surprise, we also could record this potential 7 mm in front of the retina, with the electrode in the vitreous, and 5 mm above the lateral geniculate nucleus and the superior colliculus, where there are no direct inputs from the optic tract. These results show quite clearly that field potentials can “stray” much farther than the underlying anatomical structure projects.     

Are field potentials an appropriate method for demonstrating connections in the brain?

A common technique for demonstrating projections in the brain is to electrically stimulate one part of the brain and record mass or field potentials from another part. We showed in the visual system of the cat, where connections between retina, lateral geniculate nucleus, and superior colliculus are very well known, that the recording of field potentials is not at all sufficient to demonstrate connections. The most prominent potential after electrical stimulation of the optic tract is the field potential created by the Y-ganglion cell fibers of the optic nerve. We recorded this potential in the optic nerve head of the eye, in the lateral geniculate nucleus, and in the superior colliculus. To our surprise, we also could record this potential 7 mm in front of the retina, with the electrode in the vitreous, and 5 mm above the lateral geniculate nucleus and the superior colliculus, where there are no direct inputs from the optic tract. These results show quite clearly that field potentials can “stray” much farther than the underlying anatomical structure projects.     

Triiodothyronine and Brain Excitability

We investigated mechanisms involved in thyroid hormone action on brain excitability. The effect of acute exposure of triiodothyronine (T3) to rat hippocampal slices in vitro was studied. No significant changes could be detected in prevolley, field excitatory postsynaptic potentials (fEPSP) and population spike amplitude, while there was a minor, nonsignificant trend toward shortening of the population spike latency time. T3 had no effect on penicillin-induced epileptiform activity. There was, however, an active accumulation of radioactively labeled T3 in the slices. A rat cervaux-isolé preparation was used to determine focal seizure thresholds in the visual cortex, and no acute (2-4 h) effects were demonstrated. No significant acute effects of T3 on brain excitability in the hippocampus and visual cortex was observed, despite an active accumulation of T3. Thus, the effect of T3 on brain excitability most likely is due to delayed effects.     

Disseminated lesions at presentation in patients with optic neuritis.

Thirty five adults and two children with clinically isolated optic neuritis were examined by magnetic resonance imaging (MRI) to determine the presence of disseminated lesions within the brain at presentation and to compare these findings with the results of evoked potential studies. Of the adult patients, 61% showed lesions on the scans whereas the evoked potentials suggested the presence of lesions outside the visual system in 30%. MRI is a sensitive method for the demonstration of clinically unsuspected lesions in patients with uncomplicated optic neuritis.     

Organization and metamorphosis of glia in the Drosophila visual system

The visual system of Drosophila is an excellent model for determining the interactions that direct the differentiation of the nervous system's many unique cell types. Glia are essential not only in the development of the nervous system, but also in the function of those neurons with which they become associated in the adult. Given their role in visual system development and adult function we need to both accurately and reliably identify the different subtypes of glia, and to relate the glial subtypes in the larval brain to those previously described for the adult. We viewed driver expression in subsets of larval eye disc glia through the earliest stages of pupal development to reveal the counterparts of these cells in the adult. Two populations of glia exist in the lamina, the first neuropil of the adult optic lobe: those that arise from precursors in the eye-disc/optic stalk and those that arise from precursors in the brain. In both cases, a single larval source gives rise to at least three different types of adult glia. Furthermore, analysis of glial cell types in the second neuropil, the medulla, has identified at least four types of astrocyte-like (reticular) glia. Our clarification of the lamina's adult glia and identification of their larval origins, particularly the respective eye disc and larval brain contributions, begin to define developmental interactions which establish the different subtypes of glia.     

Optogenetic field potential recording in cortical slices

We introduce a method that uses optogenetic stimulation to evoke field potentials in brain slices prepared from transgenic mice expressing channelrhodopsin-2-YFP. Cortical slices in a recording chamber were stimulated with a 473nm blue laser via either a laser scanning photostimulation setup or by direct guidance of a fiber optic. Field potentials evoked by either of the two optogenetic stimulation methods had stable amplitude, consistent waveform, and similar components as events evoked with a conventional stimulating electrode. The amplitude of evoked excitatory postsynaptic potentials increased with increasing laser intensity or pulse duration. We further demonstrated that optogenetic stimulation can be used for the induction and monitoring of long-term depression. We conclude that this technique allows for efficient and reliable activation of field potentials in brain slice preparation, and will be useful for studying short and long term synaptic plasticity.     

Origin and propagation of spontaneous electrographic sharp waves in the in vitro turtle brain: a model of neuronal synchronization.

OBJECTIVES: Neuronal synchronization is a basic feature in the generation of epileptiform discharges. Spontaneous large sharp waves (LSWs) can be recorded in the turtle brain in vitro, indicating the synchronous activation of large neuronal populations. The aim of this study was to analyze the spatial and temporal distribution of LSWs within the brain; the participation of glutamate in LSWs generation was also investigated. METHODS: Extracellular field potentials were recorded in vivo (n = 4) and in vitro (n = 36). LSWs were recorded from cerebral cortex, optic tectum, and thalamus. RESULTS: LSWs were recorded from cerebral cortex, optic tectum and thalamus. No LSWs were observed in cerebellum and brain stem. In some experiments, LSWs could be recorded only from medial cortex. Latency studies demonstrated that, within each hemisphere, medial cortex led the generation of LSWs; in addition, isolated medial cortex could sustain LSWs. Intracortical laminar field potentials in medial cortex indicated that LSWs generate mainly in the molecular layer, probably at pyramidal cell dendrites. Pharmacological experiments demonstrated that NMDA and non-NMDA glutamate receptors are involved in LWSs generation. CONCLUSIONS: These results suggest that turtle medial cortex is the pacemaker area for LSWs generation and it can be a useful model to study cellular and circuital mechanisms of neuronal synchronization.     

The isolated mammalian brain: an in vivo preparation suitable for pathway tracing

An in vitro preparation of complete brain is presented which allows successful tracing with fast axonal tracers for at least 2 days after in vitro preparation. A simple procedure is used, by which the isolated brain is submerged in oxygenated artificial cerebrospinal fluid, enabling maintenance of adequate integrity without perfusion the vascular system. The use of an isolated brain has many advantages: virtually all brain areas are easily accessible; tracer applications are possible without problems of animal survival; and the tracers are be translocated by blood circulation. The viability of this isolated brain preparation was validated by successful recording of extracellular field potentials 1 day later.     

Lens-Injury-Stimulated Axonal Regeneration throughout the Optic Pathway of Adult Rats

Axonal regrowth and restoration of visual function were studied in adult rats. The optic nerve was completely cut behind the eye. The proximal and distal nerve stumps were realigned and the meninges sutured back together. During the same surgical procedure, the lens was lesioned in order to induce secondary cellular cascades, which are known to strongly support the survival of retinal ganglion cells (RGCs) and to promote axonal regeneration. The anatomical and topographic restoration of the visual pathway was assessed neuroanatomically with the aid of anterograde and retrograde tracing using fluorescent dyes. It appeared that the axons formed growth cones at the junction of the suture soon after injury, before glial cells and extracellular matrix proteins were able to cause local scar formation. Growth cones first entered the distal optic nerve stump 3 days after injury, grew through it to reach the optic chiasm approximately 3 weeks after the lesion was made, and terminated within the retinoreceptive layers of the superior colliculus 5 weeks after lesioning. Quantification of the retrogradely labeled cell bodies within the regenerating retina revealed that up to 30% of the RGCs, which includes all major cell types, were capable of regenerating their axons along the entire visual pathway. To assess whether topography was restored, double-labeling experiments were performed, revealing only crude topographic restoration during the initial stages of regeneration. However, visual-evoked potentials could be recorded, indicating that synaptic transmission in higher visual areas was relatively intact. The data show, in principle, that cut axons can regenerate over long distances within the white matter of a central nerve like the adult optic nerve, spanning over 11 mm to the chiasm and between 12 and 15 mm to the thalamus and midbrain. The findings suggest, for the first time, that lentogenic stimulation of RGCs is sufficient to induce the formation of growth cones that can override inhibitors at the site of injury, grow through the white matter of the optic nerve, pass through the optic chiasm, and make synaptic connections within the brain.     

外伤性视交叉损伤

目的 探讨外伤性视交叉损伤的病理机制及诊断治疗.方法 对14例外伤性视交叉损伤的临床表现、影像学特点、手术治疗及随访进行研究.结果 14例病人中25只眼外伤后出现视力下降(双眼11例、单眼3例),双颞侧偏育10例,单眼颞侧偏肓4例.头颅CT示脑挫裂伤12例,头颅MRI检查11例均发现前颅窝底额叶眶直回脑挫裂伤.11例患者接受手术治疗,术后脑脊液鼻漏2例,随访6-36个月,平均13个月,10例14只眼术后视力提高、6例视野缺损有改善.3例未经手术治疗的患者,药物治疗视力皆提高,但视野无明显改善.结论 视野检查颞侧缺损及头颅MRI检查是外伤性视交叉损伤诊断首选的检查,MRI检查显示有明显视交叉压迫者应该积极手术治疗.     

Morphological and functional analysis of an incomplete CNS fiber tract lesion: graded crush of the rat optic nerve

Fiber tract lesions in the central nervous system (CNS) often induce delayed retrograde neuronal degeneration, a phenomenon that represents an important therapeutic challenge in clinical neurotraumatology. In the present study, we report an in vivo trauma model of graded axonal lesion of CNS neurons. Controlled by a newtonmeter device, we induced retrograde degeneration of adult rat retinal ganglion cells (RGCs) by graded crush of the optic nerve. The extent of secondary RGC death increased linearly with the applied crush force. Moreover, visually evoked potentials were used to characterize the consequences of controlled optic nerve lesion on the functional integrity of the visual projection. The presented model of fiber tract lesion closely resembles the clinical conditions of traumatic brain injury and could prove useful to screen for neuroprotective drugs based on both a morphological and functional read-out.     

Visual system function in patients after surgery for intracranial tumors

Visual function was studied in patients after operations for brain tumours. The study group comprised 7 cases. Visual acuity, field of vision by kinetic and static methods and visual evoked potentials were studied before and after operations. The follow up time was from 1 to 51 months, mean 20 months. In all patients decreased visual acuity, visual field defects and VEP abnormalities were found, before operation. The first control examination after operation showed improvement of visual acuity in 2 cases after removal of pituitary tumours, and worsening of vision in all the remaining ones. In two cases of tumours spreading to the basis of the frontal lobe blindness of one eye developed. Static and kinetic perimetry showed in all cases enlarged visual field defects. VEP confirmed that removal of pituitary tumours compressing visual tract can improve vision: P100 amplitudes increased and latencies become shorter. Further VEP improvement occurred even 6-20 months after achieving of good visual acuity. No improvement of vision developed if the visual pathway had been damaged during the operation. CONCLUSIONS: Pituitary tumours can be removed without damage to the surrounding structures and vision can improve after that. Meningiomas and gliomas lying in immediate vicinity of optic nerves and their chiasma or growing out from them are usually large and often their removal is associated with damage to the visual pathway leading to visual field defects to blindness. The assessment of vision should be based on static and kinetic perimetry and visual evoked potentials (VEP) since these methods are mutually complementary and only their comparison provides a full result.     

Electrophysiological properties of embryonic neocortex transplants replacing the primary visual cortex of adult rats

Solid pieces of the occipital neocortex derived from 17-day rat fetuses were placed in a cavity formed by complete unilateral aspiration of the primary visual cortex in adult rats. Vital labeling of the brain with bisbenzimide was used to differentiate grafts from the host brain tissue. 2 to 10 months after operation electrophysiological experiments were performed in which neuronal activity and field potentials in transplants were recorded in response to sensory and electrical stimulation of the host brain. This study shows that in a large portion of the transplants (14 out of 25): (1) the majority of neurons (183/270) are controlled by visual stimuli and many of them respond to electrical stimulation of the lateral geniculate body (53/62) and the homotopic sites of the contralateral neocortex (28/62); latencies of these responses are within the ranges typical of the normal visual cortex; (2) there is a topical representation of the visual field on the transplants; (3) receptive field sizes, the preference to stationary flashes or to moving visual stimuli and the temporal response pattern of the grafted neurons are similar to those of the primary visual cortex. However, the field potentials evoked visually were recorded only in part of the transplants (8/14) which revealed clear neuronal visual responses, and field potential depth profile differed from that in visual cortex in situ. The functional organization of the transplants remained unchanged throughout the long-time testing. Taken together, these results suggest that after primary visual cortex removal, fetal neocortex transplants may be able to replace functionally the damaged neural circuitries of the host brain.     

Use of evoked potentials for diagnosis of multiple sclerosis

The author discusses visual evoked potentials, brain stem auditory evoked potentials, somatosensory evoked potentials, motor evoked potentials, and MRI for the diagnosis of MS. Most patients with MS will eventually have an MRI scan. However, certain specific questions regarding function and anatomic regions are better studied with evoked potentials, especially those of optic nerve, brain stem, and spinal cord.     

Brain structures of a medaka mutant, el (eyeless), in which eye vesicles do not evaginate

Eye development and brain structures of a mutant teleost fish were investigated. The el (eyeless) mutation in medaka (Oryzias latipes) is recessive and affects eye formation; in the most severe cases, it results in the absence of eyes. Developmental studies revealed that normal eyeballs are not formed in the el mutant embryos, but small optic cup-like structures differentiate in situ in the walls of the prosencephalon without evagination. The anophthalmic el homozygous fish hatched normally, although they did not respond behaviorally to visual stimuli. A small fraction of these fish grew to adulthood. In the adult anophthalmic el homozygous fish, the brain exhibited abnormalities in several subdivisions. A pair of small abnormal protrusions was observed on the surface of the ventral telencephalon and preoptic area. Immunocytochemistry using a rhodopsin monoclonal antibody showed that opsin-positive cells were present in the abnormal structures. Bodian staining showed that the optic nerves were present near the abnormal structures, although the number of optic nerve fibers was extremely small. The optic tectum was extremely small, and the thickness of the stratum opticum and stratum fibrosum et griseum superficiale was reduced. These behavioral and morphological observations suggest that the adult anophthalmic el homozygous fish are functionally blind, although small retina-like structures were partially differentiated and persisted in the adult fish brain. Moreover, the adult anophthalmic el homozygous fish were infertile, and the sizes of the hypophysis and the hypothalamus were reduced. Thus, the el mutation affects not only the brain structures that are related to the visual system but also those related to the reproductive system.     

The electrophysiology of the olfactory-hippocampal circuit in the isolated and perfused adult mammalian brain in vitro.

The viability and general electrophysiological properties of the limbic system in the adult mammalian brain isolated and maintained in vitro by arterial perfusion are described. The isolated brain preparation combines the advantages of intact synaptic connectivity and accessibility of different areas of the encephalic mass with those of the in vitro approach, i.e., stability and control of the ionic environment. Extracellular field potential as well as intracellular recordings were performed at different levels in the limbic system of isolated adult guinea pig brains. The results demonstrate that in the piriform, entorhinal, and hippocampal cortices, the intrinsic electrical properties of individual cells as well as the spontaneous and evoked electrical activity in the neuronal ensembles they comprise, were virtually identical to those observed in vivo. The properties of the limbic system loop were determined.     

Kynurenic acid blocks suprachiasmatic nucleus responses to optic nerve stimulation

An in vitro slice preparation of the mouse hypothalamus was used to determine the effects of pharmacological agents on the field potentials that are evoked in the suprachiasmatic nucleus (SCN) by stimulation of the optic nerve. Postsynaptic components of these responses were identified by lowering the concentration of calcium in the superfusate. Bath application of kynurenate, an antagonist of excitatory amino acid neurotransmission, reversibly blocked postsynaptic responses in the SCN. The evoked responses in the SCN were not affected by the acetylcholinergic agents (+)-tubocurarine, scopolamine, physostigmine, or carbachol. These results suggest that excitatory amino acid receptors mediate responses of SCN neurons to retinal input, but do not support a role for acetylcholine.