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PubMedDate not supplied

Retinal nerve fiber layer thickness in optic tract syndrome.

BACKGROUND: Optic tract syndrome (OTS) is characterized by incongruous homonymous hemianopia and a perpendicular pattern of bilateral optic atrophy due to the optic tract lesion. However, loss of retinal nerve fiber layer thickness (RNFLT) associated with OTS has not been quantitatively assessed. CASE: A 20-year-old woman with blunt head trauma showed normal visual acuity, color vision, ocular motility, and intraocular pressure. Because of a relative afferent pupillary defect in her left eye and left-sided homonymous hemianopia, we suspected right-sided optic tract damage, although magnetic resonance imaging detected no intracranial lesion. OBSERVATIONS: Using optical coherence tomography (OCT), the RNFLT of this case was measured at 31 months after the trauma and compared with age-matched normal controls (n = 41). Nasal, temporal, superior, and inferior quadrant RNFLT was reduced by 22%, 21%, 5%, and 46% in the right eye and 76%, 64%, 25%, and 27% in the left eye, respectively. The reduction was > 3 x the standard deviation of the normal mean values in the nasal and temporal quadrants of the left eye and in the inferior quadrant of the right eye. CONCLUSIONS: OCT can determine the RNFLT reduction corresponding to the characteristic patterns of optic atrophy of OTS.

Adult↗
PubMed1991

Correlation between amount of retinal afferents to the pretectal nucleus of the optic tract and dorsal terminal accessory optic nucleus and performance of horizontal optokinetic reflex in rat.

Intraocular kainic acid injection in Long-Evans rats induces loss of retinal afferents to subcortical visual centers as assessed by the axoplasmic transport of [14C]valine. The optical terminal fields of the pretectal nucleus of the optic tract (NOT), superior colliculus and accessory optic system (AOS) nuclei appear particularly affected. Since NOT and the AOS dorsal terminal nucleus (DTN) represent the first relay station of the visuomotor pathway mediating horizontal optokinetic nystagmus (HOKR), we have studied the characteristics of HOKR after various degrees of retinal deafferentation of these nuclei induced by intraocular KA injection. Taking advantage of the arrangement of the primary optic projections to NOT-DTN, that in rats are almost entirely crossed, in each animal, monocular HOKR induced by stimulation of the injected eye was compared to monocular HOKR elicited by stimulation of the intact, ipsilateral eye. Following NOT-DTN optic denervation, HOKR gain always worsened, and in a way, that the greater the deficits of retinal afferents, the greater the HOKR inability to compensate for visual motion. Furthermore, for any given retinal denervation the higher the stimulus velocity, the greater the HOKR deficit. While the correlation between HOKR gain and the amount of retinal afferents to NOT-DTN would seem to indicate a functional homogeneity of the retinal ganglion cells sending axons to these nuclei, the finding that the extent of HOKR impairment also varied with velocity might not support the above view.

Animals↗
PubMed1992

GABAergic and non-GABAergic projections of accessory optic nuclei, including the visual tegmental relay zone, to the nucleus of the optic tract and dorsal terminal accessory optic nucleus in rat.

This study examines the non-gamma-amino butyric acid (GABA)ergic (group I neurons) and GABAergic neurons (group II neurons) of the accessory optic system projecting to the nucleus of the optic tract (NOT)/dorsal terminal nucleus (DTN) of the accessory optic system in rat. These nuclei include the dorsal (MTNd) and ventral (MTNv) divisions of the medial terminal nucleus, the lateral terminal nucleus, the interstitial nucleus of the superior fasciculus, the posterior fibers, and the visual tegmental relay zone. GABAergic neurons of these nuclei that do not target the NOT/DTN (group III neurons) have also been observed. The fluorescent retrograde tracer fluoro-gold was injected into the pretectum, targeting the NOT/DTN and the tissue prepared immunocytochemically to reveal neurons containing the neurotransmitter GABA. Three groups of neurons (groups I, II, and III neurons) were examined in terms of their distribution, density, and percentage present. Group I neurons are single-labeled with fluoro-gold and represent non-GABAergic neurons projecting to the NOT/DTN. These neurons are of the highest density in the lateral terminal nucleus (204 neurons/mm2). Their densities are also substantial in the MTNv (120 neurons/mm2), interstitial nucleus of the superior fasciculus, posterior fibers (96 neurons/mm2), and visual tegmental relay zone (93 neurons/mm2). Group II neurons are double-labeled with fluoro-gold and GABA. They form a system of GABAergic neurons projecting to the NOT/DTN, which are exceedingly dense in the MTNd (78 neurons/mm2) but are also dense in both the visual tegmental relay zone (49 neurons/mm2) and MTNv (33 neurons/mm2). Group III neurons are GABAergic neurons that do not target the NOT/DTN but must project to other brain nuclei and/or be interneurons. These are of extremely high concentration in the visual tegmental relay zone (316 neurons/mm2) and are also of substantial densities in the MTNd (77 neurons/mm2), lateral terminal nucleus (72 neurons/mm2), and MTNv (44 neurons/mm2). The MTNd has the highest percentage of GABAergic neurons projecting to the NOT/DTN (72%). GABAergic neurons also form significant percentages of the projections to the NOT/DTN from the visual tegmental relay zone (34%) and MTNv (21%). The percentage of the total GABAergic neurons that project to the NOT/DTN is the highest in the MTNd (50%) and MTNv (42%). The described GABAergic afferents to the NOT/DTN may function to process information concerned with the compensation for retinal slip.

Animals↗
PubMed1985

Topography of the goldfish optic tracts: implications for the chronological clustering model.

Both the dorsal and ventral optic tracts of goldfish have similar shapes when they are sectioned perpendicularly to their longitudinal axes. Each tract is pear-shaped, consisting of a narrow and a deep apex, a wide midspan, and a progressively curved and tapered superficial base. The tracts differ in that the apex of the dorsal optic tract points caudally, while the apex of the ventral optic tract points medially. In addition, upon segregating from the main optic tract, the dorsal optic tract courses dorsally while the ventral optic tract courses caudally. Thus, the two optic tracts have similar shapes and are orthongonal to one another. The topography of the retinal fibers within the optic tracts was determined either by ablating part of the retina and subsequently filling the axons from the intact hemiretina with cobaltous-lysine or by applying cobaltous-lysine to a slit in the retina. Both optic tracts contain a similar arrangement of optic fibers. Axons of central retinal ganglion cells (RGCs) are in the apex of each tract and optic fibers of peripheral RGCs are located along the base of each tract. Axons of temporal RGCs are located dorsally in the ventral optic tract and laterally in the dorsal optic tract, while axons of nasal RGCs are located ventrally in the ventral optic tract and medially in the dorsal optic tract. These findings indicate that the optic axons are organized as laminae. Deeper laminae contain the axons of older annuli of RGCs and superficial laminae contain the axons of younger annuli of RGCs. This type of chronological organization appears to be consistent across vertebrates.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1987

The position of the crossed and uncrossed optic axons, and the non-optic axons, in the optic tract of the rat.

The position of the crossed and uncrossed optic axons, and of the non-optic axons, within the optic tract was determined in the adult hooded rat. Horseradish peroxidase histochemistry and lesion-induced degeneration of axonal profiles were independently used to study the position of the three relevant populations of axons within the optic tract. The boundaries of the optic tract are distinct at all but its caudomedial border, where it abuts the supra-optic commissures running parallel to the fibres of the optic tract. Labelling the crossed population of optic axons, or inducing their degeneration, both demonstrate a clear caudomedial border of the optic tract, although a number of optic axons stray out of the optic tract and course within the supra-optic commissures immediately caudomedial to the tract. The uncrossed optic axons are, as a population, positioned relatively deep in the optic tract, towards its dorsal border. A few occur at further ventral positions, but their density is greatly reduced there. There is also a very thin region along the dorsalmost edge of the optic tract free of uncrossed optic axons. The relative position of the uncrossed to the crossed optic axons is discussed in the context of the mammalian optic tract as a chronological map: spatial position in the tract may reflect temporal order of axonal arrival during early development. A large population of non-optic axons belonging to Gudden's commissure courses within the boundaries of the optic tract at a relatively ventral position. They are most frequent caudomedially, and are absent rostrolaterally. Hence, axons of the optic tract and Gudden's commissure are substantially intermingled in the caudomedial half of the optic tract. These non-optic axons greatly outnumber the uncrossed optic axons, and will consequently distort counts of uncrossed optic axons based on intact profiles that remain after removal of the opposite eye. However, they are still a minority in comparison to the crossed optic axons in this region.

Animals↗
PubMed2004

Characterization of a chondroitin sultate proteoglycan associated with regeneration in goldfish optic tract.

Regeneration of goldfish optic nerve axons is accompanied by a major increase in axonally transported proteoglycans (21). To identify specific proteoglycans increased during regeneration, we have used proteoglycan preparations from regenerating goldfish optic tracts to produce monoclonal antibodies. Western blot analysis shows a 28-kD antigen reacting with our 1G4/G5 antibody is present in optic tract 21 days after nerve crush, but absent in nonregenerating tract. Treatment with chondroitinase AC removes IG4/G5 immunostaining of the 28-kD molecule. An anti-CS antibody further confirmed this molecule as a chondroitin sulfate proteoglycan. A slightly smaller core protein following chondroitinase AC treatment indicates a low level of glycosylation. The N-terminal amino acid sequence of its core protein is not similar to any known proteoglycans. The CSPG sediments through 1.4 M sucrose, indicative of an extracellular matrix localization. It is expressed during the outgrowth of regenerating axons. Cut nerve and retinal explant studies demonstrate that the 1G4/G5 CSPG is not axonal, suggesting a glial localization.

Amino Acid Sequence↗
PubMed1982

The Marcus Gunn pupil in incomplete optic tract hemianopias.

Three patients with optic tract lesions, incomplete homonymous hemianopias, and good vision in both eyes are presented. All three had a Marcus Gunn pupil in the eye with temporal field loss (eye contralateral to the tract lesion). This pupillary sign may serve to differentiate acute optic tract from acute geniculostriate lesions when the characteristic infrageniculate optic atrophy has not had time to develop.

Adult↗
PubMed1992

Fiber order in the opossum's optic tract.

The distribution of axons by size in the optic tract of the South American opossum, Didelphis marsupialis was studied. Thin and semi-thin sections were examined, and measurements of axonal diameter were made on electron micrographs taken from various locations across the optic tract of normal opossums. In order to determine the contributions of the different axon diameter classes to the crossed and uncrossed retinofugal pathways, measurements were also made from the tracts of opossums in which one eye had been enucleated 5 weeks previously. Within the opossum's optic tract, the axons are partially segregated by their size: the deepest parts of the tract contain only fine and medium-sized axons, whereas coarse axons are also present superficially. In the middle of the tract, all three size classes are present. At increasingly superficial positions, there is a steady reduction in the proportion of medium-diameter axons, and an increase in the number of the finest axons. Medium and coarse axons contribute to both the crossed and uncrossed pathways, and the uncrossed component is displaced superficially relative to the crossed component. The fine axons in the deeper parts of the tract arise from both retinae, while those in the superficial parts of the tract, near the pial surface, are virtually all crossed. The opossum's optic tract thus displays the segregation of axons by size found in placental mammals, and follows a pattern reminiscent of that found in carnivores. Such a common organizational plan, particularly the similarities between the didelphids and carnivores, is suggestive of an early acquisition of parallel visual pathways in mammalian phylogeny. Since the fiber order in the optic tract of eutherians is a chronological map of axonal arrival during development, these results suggest that a conserved developmental mechanism has led to a common organizational plan.

Animals↗
PubMed2006

Slits contribute to the guidance of retinal ganglion cell axons in the mammalian optic tract.

RGC axons extend in the optic tracts in a manner that correlates with the expression in the hypothalamus and epithalamus of a soluble factor inhibitory to RGC axon outgrowth. Additionally, although the RGC axons extend adjacent to the telencephalon, they do not normally grow into this tissue. Here, we show that slit1 and slit2, known chemorepellents for RGC axons expressed in specific regions of the diencephalon and telencephalon, help regulate optic tract development. In mice lacking slit1 and slit2, a subset of RGC axons extend into the telencephalon and grow along the pial surface but not more deeply into this tissue. Surprisingly, distinct guidance errors occur in the telencephalon of slit1 -/-; slit2 +/- and slit1/2 -/- embryos, suggesting that the precise level of Slits is critical for determining the path followed by individual axons. In mice lacking both slit1 and slit2, a subset of RGC axons also project aberrantly into the epithalamus, pineal and across the dorsal midline. However, many axons reach their primary target, the superior colliculus. This demonstrates that Slits play an important role in directing the guidance of post-crossing RGC axons within the optic tracts but are not required for target innervation.

Animals↗
PubMed1985

Age-related fiber order in the optic tract of the ferret.

In the ferret's optic tract, the position of retinofugal fibers has been related to their relative age by preferentially labeling the oldest fibers. It has been found that fiber order perpendicular to the pial surface represents the sequence of axon arrivals in the optic tract, the fibers furthest from the pia being the oldest. Immature ferrets, less than 34 days post-conception (E34), were given intravitreal injections of lectin-bound horseradish peroxidase or of 3H-amino acids. After survival times of 24 hr or less, the contralateral optic tract was uniformly labeled, whereas with longer survival times unlabeled zones were seen next to the pial border. These unlabeled zones were largest after injections into the youngest animals but were never seen when injections were made after E34, no matter what the survival time. The unlabeled zones were seen in the tracts of animals having unlabeled regions in the periphery of the retina. The unlabeled retinal ganglion cells are interpreted as ganglion cells formed after the injection was made, and unlabeled axons next to the pia in the tract are interpreted as the axons of these youngest cells. Some irregularities in the layered arrangement of the tract are described, and the fiber order in the tract is contrasted with that in the optic nerve behind the eye. It is shown that tract order is partially independent of order in the intraorbital part of the optic nerve. Between the retina and the optic tract, a sorting of fibers occurs not only in terms of the pattern of decussation, but also in terms of fiber age.

Aging↗
PubMed1989

Representation of the temporal raphe within the optic tract of the cat.

The retinal topography of the cat's optic tract was determined by means of injections of the enzyme horseradish peroxidase (HRP) into the tract. This analysis was accomplished by the subtraction of all HRP injection sites not labeling a defined retinal area from those injection sites which resulted in ganglion cell labeling (Venn diagram analysis). Using this method, the following correspondences were demonstrated for the ipsilateral and contralateral projections: superior retina represented in medial optic tract; inferior retina in lateral tract; and area centralis in a dorsocentral location (which was part of a larger area representing the visual streak). The temporal raphe was represented in the ipsilateral tract as a band curving from the area centralis region toward the dorsomedial border of the tract. Contralateral fibers from a region superior to the optic disc were found to be displaced with respect to the general retinal representation in the optic tract and this appeared to be related to retinal development. The ratio of contralateral to ipsilateral fibers was determined and found to be nonuniform within the tract. Injection of HRP into the optic tract of the cat also allowed the axons from labeled retinal ganglion cells to be traced within the retina and optic disc. Axons from ganglion cells lying temporal to the raphe curve around the area centralis enter the optic disc on the lateral and inferior aspects. Ganglion cells lying nasal to the raphe send their axons more directly to enter the optic disc on its superior aspect. A schema is proposed whereby the retina is mapped onto the optic tract.

Animals↗
PubMed1984

Fibre order in the normal Xenopus optic tract, near the chiasma.

In juvenile Xenopus retinotopic fibre order in the optic tract near the chiasma was investigated by labelling small groups of optic fibres from peripheral retina with HRP. This selective fibre labelling with HRP was combined with autoradiography following administration of tritiated thymidine to the eye, so that the HRP-labelled fibres could be located within the borders of the optic tract. Fibres arising from the periphery of all four retinal quadrants were superficially located in the optic tract near the chiasma, with dorsal retinal fibres showing the greatest tendency to travel deep in the diencephalon. Retinal lesions closer to the optic nerve head labelled fibres which ran deeper in the optic tract. Near the chiasma, fibres from ventral retina tended to group rostrally while fibres from dorsal retina tended to group caudally. However, no obvious localization of fibres arising in temporal or nasal retina was seen in the lower optic tract.

Age Factors↗
PubMed2000

Cortical and subcortical influences on the nucleus of the optic tract of the opossum.

In the present work we propose a new phylogenetic hypothesis for the role played by cortical and subcortical afferents to the nucleus of the optical tract, the main visual relay station of the horizontal optokinetic reflex in mammals. The hypothesis is supported by anatomical and physiological data obtained in the South American opossum (Didelphis aurita) using the following experimental approaches: (i) single-unit recordings in the nucleus of the optic tract and simultaneous electrical stimulation of the contralateral nucleus of the optic tract; (ii) single-unit recordings in the nucleus of the optic tract and simultaneous electrical stimulation of the ipsilateral striate cortex; (iii) injection of cholera toxin subunit B into the striate cortex and subsequent immunohistochemical reaction to reveal the presence of the marker in the thalamus and mesencephalon; and (iv) single-unit recordings in the nucleus of the optic tract both before and after ablation of the ipsilateral visual cortex. The main results are: (i) there is a strong inhibitory reciprocal effect upon the nucleus of the optic tract following stimulation of its contralateral counterpart; (ii) electrophysiological and anatomical data imply that the visual cortex does not project directly to the nucleus of the optic tract. Rather, cortical terminals seem to target the nearby anterior and posterior pretectal nuclei and orthodromic latencies in the nucleus of the optic tract following stimulation of the visual cortex were twice as large as in the superior colicullus; and (iii) ablation of the entire visual cortex did not have any effect upon binocularity of cells in the nucleus of the optic tract. These results strengthen the model proposed here for the role of the interactions between the nuclei of the optic tract under optokinetic stimulation. The hypothesis in the present work is that the cortical influences upon the nucleus of the optical tract, in addition to the subcortical ones, appeared only recently in phylogenesis. In more primitive mammals, such as the opossum, subcortical interactions are thought to play a relatively important role. With the emergence of retinal specializations, such as the fovea, one might suppose that there followed the appearance of new ocular movements, such as the smooth pursuit and certain types of saccades, that came to join the pre-existent optokinetic reflex.

Animals↗
PubMed1986

Retinal topography in the optic tract of adult goldfish.

The present study was aimed at determining how transformations in fiber order establish a retinal topography in the optic tract of adult Carassius auratus. Horseradish peroxidase was applied to the optic nerve or retina, and the pathways of labeled axons originating from retinal annuli or wedges were analysed in reconstructed serial-sections and wholeamounts of the optic pathway. The age-related fiber order of the optic tract involves a rotation of the optic pathway that begins near the chiasm, continues through the optic tract as it wraps around the brain, and extends through the brachia. The relative order of laminae, in which each lamina is composed of age-related axons, is maintained in the optic pathway. The laminae add systematically onto the optic tract in a mediolateral direction with the oldest lamina forming the medial margin. Retinal sector order in the optic tract is established by the rearrangement of axons from each lamina. These rearrangements begin at the chiasm and, in part, involve transposition of axons originating from the ventrotemporal and dorsonasal sectors of the retina. The transformations achieve a fiber order in the optic tract that is appropriate for entry into the tectum. It is proposed that the final retinal topography of the optic tract is determined by the combined influences of selective affinities along the neural axis and substrate guidance mechanisms, the latter being mediated largely by the oldest axons of the fasciculus medialis tractus opticus.

Animals↗
PubMed1989

Cavernous angioma of the optic tract.

A cavernous angioma of the right optic tract in a 35-year-old man is presented. The patient suffered from headaches and had a left homonymous visual field defect after subarachnoid haemorrhage and an intracerebral haematoma in the right temporomedial region, revealed by computed tomography (CT). Follow-up CT showed a small contrast-enhanced lesion in the right suprasellar and parasellar cistern. Angiography on three occasions did not reveal a vascular lesion. Magnetic resonance imaging was helpful both for diagnosis and planning surgical therapy. It showed typical signs of a cavernous angioma of the right optic tract; the diagnosis was confirmed by surgery and histological examination. This appears to be the first reported case of a cavernous angioma of the optic tract.

Adult↗
PubMed1975

Anatomical studies on the optic tract (tractus opticus) of the Indian buffalo (Bubalus bubalis).

The optic tract of the buffalo was found to begin from the posterolateral angle of the chiasma, from where it extended laterally for about 8 mm. Each tract was round in its initial portion, but was flattened subsequently. In its course to the corpus geniculatum laterale (CGL), it swept round the homolateral cerebral peduncle. The tract fibres entered the CGL chiefly on its ventrolateral aspect. The optic fibres appeared to enter the CGL as individual fibres. The fibres in the optic tract were mostly myelinated. There were 253823 +/- 27534-254800 +/- 29232 myelinated fibres in it. There was no fascicular arrangement of these fibres. The calibre of the myelinated fibres in the optic tract varied from 1-12 microns. A fibre diameter analysis revealed an unimodal distribution of these fibres with a peak at 2 microns. Thinner fibres predominated in the peripheral portion of the optic tract. In the central portion, fibres of larger diameter were seen in greater numbers.

Animals↗