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PubMed1977

The visual cortex of the opossum: the retrograde transport of horseradish peroxidase to the lateral geniculate and lateral posterior nuclei.

The visual cortex of opossum was studied by injecting horseradish peroxidase into the cortex and identifying labeled neurons in the thalamus. The results show that the lateral geniculate nucleus projects to area 17 in a topographical manner: the rostral lateral geniculate is represented in caudal striate cortex, and the dorsal extremity of the lateral geniculate, which probably corresponds to the zero vertical meridian, is represented along the border of area 18. Small injections in area 17 produced restricted bands of labeled neurons across the medial-lateral extent of the lateral geniculate, suggesting a greater precision in the topography than previously shown by retrograde degeneration studies. Following injections into area 17, labeled cells were also found in the lateral posterior nucleus. Injections of peristriate cortex produced labeled cells in the lateral posterior nucleus, as well as the lateral intermediate, posterior and intralaminar nuclei. Since the lateral posterior nucleus receives visual projections from the superior colliculus, the results show two visual pathways: the geniculo-striate path projecting just to core area or area 17, and a more diffuse parallel path that projects to both the core and belt. Whether or not this overlap is characteristics of the mammalian prototype it seems to be present in widely separated species.

Animals↗
PubMed2000

Topographic order of retinofugal axons in a marsupial: implications for map formation in visual nuclei.

We studied axon order in the primary visual pathway and in nine retinorecipient nuclei of a small marsupial, the fat-tailed dunnart (Sminthopsis crassicaudata) using animals at postnatal day (P) 40 and P80. Dorsal, ventral, nasal, and temporal axons enter the optic nerve true to their retinal origin being respectively dorsal, ventral, medial, and lateral; the arrangement is retained to the chiasm. Dorsal and ventral axons maintain their respective locations within the chiasm but at the base of the contralateral optic tract undergo a 180 degrees axial rotation, thus reversing the dorsoventral axis with respect to the retina. The alignment is conserved along the optic tract with dorsal and ventral axons mapping directly into appropriate quadrants of each retinorecipient nucleus. Nasal and temporal axons remain segregated as they decussate and lie respectively superficially and deep along the optic tract but with some intermingling. Within each retinorecipient nucleus, the nasotemporal axis is clearly demarcated, being represented in either a rostrocaudal (ventral and dorsal lateral geniculate nuclei; lateral posterior, dorsal terminal, and pretectal nuclei) or caudorostral (medial terminal and caudal pretectal nuclei, intergeniculate nucleus and superior colliculus) direction. The results imply that the dorsoventral axis in the retinorecipient nuclei could be due to preordering within the pathway, whereas the nasotemporal axis is determined by target-based cues. Moreover, cues for the orientation of the nasotemporal axis within retinorecipient nuclei must be localised within individual nuclei rather than as a single organiser, as previously envisaged (Chung and Cooke [1978] Proc. R. Soc. Lond. B. 210:335-373).

Animals↗
PubMed1999

Early intervention for children with cerebral visual impairment: preliminary results.

According to the ophthalmological literature, cerebral visual impairment (CVI) is defined as a temporary or permanent visual loss caused by a disturbance of the posterior visual pathways and/or occipital lobes. The study of CVI is still a new field, and diagnosis is frequently difficult and sometimes may not even be considered. Different studies have taken into account various aetiologies of CVI. Neurological problems are common findings in children with CVI and this population may also show ocular abnormalities. The present study reviews the clinical history of 76 patients who have been examined at the Robert Hollman Foundation, Cannero, Italy, over the past 3 years. Infants and children were studied from birth to 4 years of age from both a neurological and an ophthalmological point of view. Taking the development of the children into account, responses to visual stimulation were analysed in order to compare the behaviours exhibited by the sample with those described in literature.

Age Factors↗
PubMed1997

Imaging findings in patients with clinical anophthalmos.

PURPOSE: To review the intracranial and facial imaging features in children with congenital anophthalmos. METHODS: We retrospectively studied eight children with anophthalmos with respect to intraorbital, intracranial, and craniofacial anomalies (six had CT examinations, including the face, orbits, and brain, and four had MR imaging, including the orbits and brain). RESULTS: Three patients had primary bilateral anophthalmos on CT (n = 1) and MR (n = 3) studies. In these patients, MR images showed hypoplasia of the optic chiasm and posterior visual pathways (n = 3), agenesis (n = 1) or dysgenesis of the corpus callosum (n = 2), and a mass in the tuber cinereum region (n = 1). One patient had incontinentia pigmenti. Five patients had unilateral anophthalmos on CT (n = 5) and MR (n = 1) studies. One of these patients had a contralateral congenital cystic eye and one had contralateral severe microphthalmia and absent optic chiasm. All had craniofacial anomalies that consisted of midline facial clefts (n = 2) and concomitant hemifacial hypoplasia (n = 2). One had a craniosynostosis. All five had normal-appearing brains. CONCLUSION: Patients with bilateral anophthalmos represent a distinct group from those with unilateral anophthalmos. In our patients, bilateral anophthalmos was associated with absence of the optic chiasm, diminished size of the posterior optic pathways, and agenesis or dysgenesis of the corpus callosum. Patients with unilateral anophthalmos had severe craniofacial anomalies. Imaging of the face is helpful in patients with unilateral anophthalmos.

Agenesis of Corpus Callosum↗
PubMed1981

[Efferent and afferent connections of the nucleus lateralis posterior thalami ("pulvinar") in the albino rats (author's transl)].

The efferent and afferent connections of the lateral posterior nucleus (LP) of the albino rat were investigated light microscopically with the silver-degeneration-methods and the HRP-methods as well. The results are: 1. The main projection region of the LP is the area of 18a of the peristriate visual cortex. Most degenerating axons terminate in layer IV. A few fibers pass layers III and II and terminate in layer I. It is not sure if there are also terminating fibers in layer IV. We could not find a topistic relation between LP and area 18 a. 2. We observed a small number of degenerating fibers in area 17, too. 3. A part of the degenerating fibers runs to the temporal cortex end enters area 20. 4. There is no evidence for a projection of the LP to both the subcortical regions and to the superior colliculus. 5. The majority of the LP's afferent fibers originates - on the subcortical level - from the superior colliculus. Especially the lamina III (Str. opticum) of the ipsilateral and of the contralateral side is here the source of fibers terminating in the LP. 6. Other subcortical sources of fibers terminating in the LP are: the pretectal region, the ventral part of the LGN, the Zona incerta, the thalamic reticular formation, and the dorsal raphe nucleus. 7. There exists a fiber projection of the area 17 to the LP. The axons originate mainly from pyramidal cells in layer V. It is discussed whether the area-17-fibers terminating in the LP are collaterals of the fibers terminating in the superior colliculus. The projection of the area 18a to the LP is of greater importance. The axons of this area originate mainly from cells of the layer VI. It becomes obvious that the thalamic relay-station of the second visual pathway seems to project nearly exclusively to the neocortex. In contrast to the dorsal LGN, however, the LP is not only a simple relay-station for visual information as also non-visual information arrives here. The morphological basis for these inputs has not yet been clarified completely. We have to take into consideration as well as the connections with the superior colliculus and the pretectal region and the cortical connections. It is remarkable that there exists also a projection of LP-fibers to a region outside the classical visual cortex. In mammals of higher evolution that kind of projection extends increasingly. It is discussed if - under comparative-anatomical aspect - the morphological changes in the pulvinar region are an expression of the neocorticalization, whereas the morphological changes in the dorsal LGN reflect mainly the functional specialization of the visual system.

Afferent Pathways↗
PubMed2007

Neuro-ophthalmology for neuroradiologists.

Combining an understanding of neuro-ophthalmologic anatomy with proper imaging techniques provides a powerful method to detect lesions involving the afferent and efferent visual pathways. Precise documentation of the extent of injury within the nervous system is becoming increasingly important to assess and monitor the effect of neurologic therapies. This review will focus on those common neuro-ophthalmologic problems that have exquisite localizing value on neuro-imaging.

Brain↗
PubMedDate not supplied

Ascending projections from the optic tectum in the lizard Podarcis hispanica.

The ascending projections of the optic tectum, including their cells of origin, have been studied in the lizard Podarcis hispanica by means of a two-step experimental procedure. First, tracers were injected in the tectum to study the anterograde labeling in the forebrain. Second, the cells of origin of these projections have been identified by analyzing the retrograde labeling after tracer injections in the thalamus, hypothalamus, and pretectum. Three main tectal ascending pathways have been described: the dorsal tecto-thalamic tract (dtt), the medial tecto-thalamic tract (mtt), and the ventral tecto-thalamic tract (vtt). The dtt originates in radial cells of layers 5 and 7 and bipolar cells of layers 8 and 10 that project to the lateral neuropile of the dorsal lateral geniculate nucleus (GLD), to the intergeniculate leaflet (IGL), and to the ventral lateral geniculate nucleus (GLV). The mtt arises from radial neurons of layers 3 and 5 and bilaterally reaches the putative reticular thalamus and its boundary with the hypothalamus, the rostral IGL, and the area triangularis (AT). The vtt is composed of fibers from ganglion and multipolar cells of the layer 7 that project bilaterally to the nucleus of the vtt, the ventrolateral thalamic nucleus, the medial posterior thalamic nucleus (MP), the nucleus rotundus (Rot), the IGL, and the cell plate of the GLD. Therefore, the GLD receives not only direct retinal afferents but also two different tectal inputs, thus constituting a convergence point in the two visual pathways to the telencephalon. Moreover, different tectal cells specifically project to the ventrolateral thalamus and to pretectal nuclei. These results are discussed from comparative and functional viewpoints.

Animals↗
PubMed1997

Knowing where and knowing what: a double dissociation.

We report a double dissociation between visuo-spatial abilities and semantic knowledge (knowledge of the names and attributes of objects and people), in two brain-injured people with longstanding stable impairments, using a wide range of tests to explore the extent of the dissociation, MU, who has bilateral lesions of occipito-parietal cortex, shows severe spatial disorientation with relatively well-preserved semantic knowledge. He is contrasted with JBR, who has bilateral temporal lobe damage and shows severe semantic problems and no impairment on visuo-spatial tasks. Our findings thus demonstrate a double dissociation between the performance of semantic and spatial tasks by MU and JBR. This pattern is consistent with Ungerleider and Mishkin's (1982) neurophysiological hypothesis of separable cortical visual pathways; one which is specialised for spatial perception and follows a dorsal route from occipital to parietal lobes, and the other following a more ventral route from occipital to temporal lobes, whose target is semantic information needed in specifying what an object is.

Adult↗
PubMed2002

Visual field defects and neural losses from experimental glaucoma.

Glaucoma is a relatively common disease in which the death of retinal ganglion cells causes a progressive loss of sight, often leading to blindness. Typically, the degree of a patient's visual dysfunction is assessed by clinical perimetry, involving subjective measurements of light-sense thresholds across the visual field, but the relationship between visual and neural losses is inexact. Therefore, to better understand of the effects of glaucoma on the visual system, a series of investigations involving psychophysics, electrophysiology, anatomy, and histochemistry were conducted on experimental glaucoma in monkeys. The principal results of the studies showed that, (1) the depth of visual defects with standard clinical perimetry are predicted by a loss of probability summation among retinal detection mechanisms, (2) glaucomatous optic atrophy causes a non-selective reduction of metabolism of neurons in the afferent visual pathway, and (3) objective electrophysiological methods can be as sensitive as standard clinical perimetry in assessing the neural losses from glaucoma. These experimental findings from glaucoma in monkeys provide fundamental data that should be applicable to improving methods for assessing glaucomatous optic neuropathy in patients.

Animals↗
PubMed2004

Setting boundaries: brain dynamics of modal and amodal illusory shape completion in humans.

Normal visual perception requires differentiating foreground from background objects. Differences in physical attributes sometimes determine this relationship. Often such differences must instead be inferred, as when two objects or their parts have the same luminance. Modal completion refers to such perceptual "filling-in" of object borders that are accompanied by concurrent brightness enhancement, in turn termed illusory contours (ICs). Amodal completion is filling-in without concurrent brightness enhancement. Presently there are controversies regarding whether both completion processes use a common neural mechanism and whether perceptual filling-in is a bottom-up, feedforward process initiating at the lowest levels of the cortical visual pathway or commences at higher-tier regions. We previously examined modal completion (Murray et al., 2002) and provided evidence that the earliest modal IC sensitivity occurs within higher-tier object recognition areas of the lateral occipital complex (LOC). We further proposed that previous observations of IC sensitivity in lower-tier regions likely reflect feedback modulation from the LOC. The present study tested these proposals, examining the commonality between modal and amodal completion mechanisms with high-density electrical mapping, spatiotemporal topographic analyses, and the local autoregressive average distributed linear inverse source estimation. A common initial mechanism for both types of completion processes (140 msec) that manifested as a modulation in response strength within higher-tier visual areas, including the LOC and parietal structures, is demonstrated, whereas differential mechanisms were evident only at a subsequent time period (240 msec), with amodal completion relying on continued strong responses in these structures.

Adult↗
PubMed1986

Visual evoked response in head trauma: pattern-shift stimulus.

Studies of visual evoked potentials in head injuries have all utilized the flash stimulus. We studied the efficacy of monocular pattern-shift visual evoked potentials (PSVEPs) in eliciting residual dysfunction of the visual pathways in 33 patients 6 to 24 months after head injury. Those with ocular trauma or ocular pathology were not included. Abnormal PSVEPs were seen in one-third of 33 head-injured patients. Only 1 (11%) of 9 patients with mild cognitive impairment had abnormal PSVEPs compared with 7 (39%) of 18 with moderate and 3 (50%) of 6 with severe cognitive impairment.

Adolescent↗
PubMed2003

Stereoscopic processing in the human brain as a function of binocular luminance rivalry.

We investigated the neural substrates of a recent model of human stereodepth perception by obtaining measurements of regional cerebral blood flow (rCBF) using PET. Subjects experienced the perceptual properties of stereopsis by viewing rival-luminance stereograms displaying an identical random-dot pattern in their central portion while the backgrounds exhibited correspondent dots contrasting in black/white luminance. The stereoscopic vision induced by retinal luminance rivalry coincided with a significant elevation of rCBF in the dorsal visual pathway. Area V5 (MT) was activated bilaterally by the experimental condition while the remaining active loci were restricted to the right hemisphere. The neural sites that responded to this novel stereoscopic stimulus are similar to those activated by traditional stereograms containing horizontal disparities.

Adult↗
PubMed1976

[Problems posed by the interpretation of peroxidase labelling of various neurons in Cyprinidae].

The origin of a centrifugal visual pathway in Cyprinids could not be demonstrated with the technique involving the labelling of cell bodies by retrograde transport of Horseradish Peroxidase. The hypothalamic labelling following intraocular injection of HRP is localized in neurosecretory structures which take up the enzyme that has passed into the circulatory system. Identical results were obtained following direct intracardiac injection. Thus extreme caution must be taken in attempting to interpret HRP results.

Animals↗
PubMed1978

A sensory mechanism for amblyopia: psychophysical studies.

Psychophysical investigations of the effect of amblyopic process on the sustained and transient channels in the afferent visual pathway are reported. The experiments on photopic luminosity, increment-threshold spectral sensitivity, spatial contrast sensitivity, and reaction-time measures of suprathreshold grating detection provide converging evidence that in naturally occuring amblyopia of humans, the sustained neural channels are more severely affected than the transient channels. However, it appears that the sustained channels are not totally nonfunctional, but rather have a higher intensity requirement than normal.

Amblyopia↗
PubMed2002

Neuroradiologic screening in normal-pressure glaucoma: study results and literature review.

PURPOSE: To determine if there was an increased prevalence of intracranial compressive lesions in patients with clinically diagnosed normal-pressure glaucoma compared with a group of patients with progressive primary open-angle glaucoma. PATIENTS AND METHODS: In a prospective, comparative, observational case series, the authors performed cranial magnetic resonance imaging in patients with consecutively diagnosed normal-pressure glaucoma (n = 62) and progressive primary open-angle glaucoma with controlled intraocular pressures (n = 70). The prevalence of intracranial compressive lesions, demographic data, and clinical characteristics were compared between both groups. RESULTS: Four of the 62 (6.5%) patients with normal-pressure glaucoma had clinically relevant intracranial compressive lesions involving the anterior visual pathway, compared with none of the 70 patients with primary open-angle glaucoma (P = 0.039). CONCLUSIONS: Intracranial compressive lesions are an important diagnostic consideration in the workup of normal-pressure glaucoma.

Adenoma↗
PubMed1985

Lobular distribution of visual climbing fiber responses in the cerebellum.

The visual pathway was electrically stimulated at the optic disc, optic nerve and pretectal region in the albino rat. Field potentials of climbing fiber activation of Purkinje cells were explored in a large area of the cerebellum, and obtained in flocculus and posterior vermis. The responses in the posterior vermis were identified in the medial region of lobules VIa-c, VIII, IX, and the dorsal region of lobule X of Larsell. No response was obtained in lobule VII.

Animals↗
PubMed1996

Evidence for a neural mechanism that encodes angles.

We measured the discrimination threshold (delta theta)Th for angle theta, where theta was either the angle of a Vee composed of two straight lines contained within the frontoparallel or the angle intersection of two straight lines contained within the frontoparallel plane. The two-line pattern was rotated bodily through a random angle between trials with the aim of eliminating the absolute orientation of one or the other line as a reliable cue to the task. We report evidence that this aim was achieved. Our main conclusion is that the ability to discriminate a change in angle theta cannot entirely be explained in terms of the ability to discriminate changes in the orientations of the individual lines that comprise the Vee. We propose that the human visual pathway contains a neural mechanism that encodes the difference in the orientations of two simultaneously-presented straight lines. Discrimination threshold for angle (delta theta)Th is roughly twice orientation discrimination threshold for an isolated line. When subjects cannot use the orientation of one or another line as a cue to the task, the plot of (delta theta)Th vs theta is approximately flat between the delta = 20 and 160 deg.

Cues↗
PubMed2005

The selection of intended actions and the observation of others' actions: a time-resolved fMRI study.

Whenever we plan, imagine, or observe an action, the motor systems that would be involved in preparing and executing that action are similarly engaged. The way in which such common motor activation is formed, however, is likely to differ depending on whether it arises from our own intentional selection of action or from the observation of another's action. In this study, we use time-resolved event-related functional MRI to tease apart neural processes specifically related to the processing of observed actions, the selection of our own intended actions, the preparation for movement, and motor response execution. Participants observed a finger gesture movement or a cue indicating they should select their own finger gesture to perform, followed by a 5-s delay period; participants then performed the observed or self-selected action. During the preparation and readiness for action, prior to initiation, we found activation in a common network of higher motor areas, including dorsal and ventral premotor areas and the pre-supplementary motor area (pre-SMA); the more caudal SMA showed greater activation during movement execution. Importantly, the route to this common motor activation differed depending on whether participants freely selected the actions to perform or whether they observed the actions performed by another person. Observation of action specifically involved activation of inferior and superior parietal regions, reflecting involvement of the dorsal visual pathway in visuomotor processing required for planning the action. In contrast, the selection of action specifically involved the dorsal lateral prefrontal and anterior cingulate cortex, reflecting the role of these prefrontal areas in attentional selection and guiding the selection of responses.

Adult↗