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At least 19 recordsLinked to original sources

[Arterial microcirculation in the optic chiasm, optic tracts and lateral geniculate bodies].

OBJECTIVES: The purpose of this study was to point out the microscopic vessels in the optic chiasm, optic tracts and lateral geniculate bodies. MATERIAL AND METHODS: This study was carried out on 20 brains, fixed in formaldehyde 10% and dissected under the surgical microscope. The material was summated to histological techniques on paraffin and performed on routine coloration. RESULTS: The lateral borders of the optic chiasm have more perforant branches as the median zone. The anterior and posterior segments of the optic tracts are rich in capillary vessels. The arteriolar branches penetrate into the lateral geniculate body on his inferior surface and borders. CONCLUSIONS: The knowledge of the arteriolar distribution in this segments of the optic pathways can explain the visual defects in some neuroophthalmologic syndromes.

Arterioles↗

Radiation necrosis of the optic chiasm, optic tract, hypothalamus, and upper pons after radiotherapy for pituitary adenoma, detected by gadolinium-enhanced, T1-weighted magnetic resonance imaging: case report.

A 26-year-old woman was treated for a prolactin secreting pituitary adenoma by surgery and radiotherapy (5860 rads). Fourteen months later, she developed right hemiparesis and dysarthria. A T1-weighted magnetic resonance imaging scan using gadolinium contrast showed a small, enhanced lesion in the upper pons. Seven months later, she had a sudden onset of loss of vision, and radiation optic neuropathy was diagnosed. A T1-weighted magnetic resonance imaging scan showed widespread gadolinium-enhanced lesions in the optic chiasm, optic tract, and hypothalamus. Magnetic resonance imaging is indispensable for the early diagnosis of radiation necrosis, which is not visualized by radiography or computed tomography.

Adenoma↗

Cavernous hemangioma of optic chiasm, optic nerves and right optic tract. Case report and review of literature.

Diminishing right ocular visual acuity for three weeks in a 30 year old man was confirmed by examination. Bilateral scotomata and bitemporal hemiachromatopsia indicated a chiasmal lesion; reduced visual acuity and Marcus Gunn pupil of the right eye and left relative temporal hemianopia indicated asymmetric involvement. Erythrocytes in the CSF verified a suspected subarachnoid bleed; contrast-enhanced CAT scan demonstrated a suprasellar mass. A cystic, multiloculated, bluish mass distorted the right optic nerve, tract, and chiasm. A hematoma was evacuated and biopsy revealed a cavernous hemangioma of the right optic nerve. Post-operatively, visual acuity has recovered in the right eye but a left homonymous temporal hemianopia has developed.

Adult↗

Solitary metastasis of breast carcinoma in the optic chiasm.

Optic chiasmatic compression from suprasellar metastatic lesions is well known, but metastasis intrinsic to the optic chiasm has not been reported. A 45-year-old woman, with treated breast carcinoma, presented with headache and chiasmatic syndrome from a large suprasellar tumour. At surgery, an exophytic chiasmatic tumour was encountered, with an appearance similar to a glioma. The pathological appearance was consistent with the primary neoplasm in the breast.

Breast Neoplasms↗

VIP fibers in rat optic chiasm and optic nerve arising from the hypothalamus.

This is the first report showing VIP fibers in the optic chiasm and the optic nerves of intact rats. These fibers form a fan-shaped dorso-medial bundle in the optic nerves. After colchicine injection into the vitreous body VIP fibers could be followed farther in the optic nerve toward the eye when compared to intact rats. After removal of eyes (enucleation) the VIP fiber-bundle became more prominent and VIP immunoreactive perikarya appeared in the supraoptic and para ventricular nuclei. When five-nine months after the enucleation Phaseolus vulgaris leucoagglutinin was administered to the paraventricular or supraoptic area, the anterogradely transported tracer was demonstrated in the optic nerve. These observations suggest the existence of a hypothalamic projection to the eye, which is, at least in part, VIP immunoreactive.

Animals↗

MRI of optic chiasm and optic pathways.

Eight verified lesions of the optic chiasm were examined on 0.5 T magnetic resonance (MR) and GE 9800, 8800 computed tomographic (CT) scanners. Enlargement of the optic chiasm was demonstrated in all cases. There was some change of MR signal compared with brain in all but one case, which had no resemblance to contrast enhancement on CT scans. The signal was specific for hematoma in one case. Abnormal signal, probably signifying tumor spread into the optic radiation, was detected on T2-weighted images in one case. The resolution of MR scans is similar or superior to CT, and sagittal views are most useful in evaluating lesions in this location.

Adolescent↗

Presence of LHRH (luteinizing hormone-releasing hormone) fibers in the optic nerve, optic chiasm and optic tract of the adult rat.

In mammals LHRH (luteinizing hormone-releasing hormone) is synthesized and released by a set of neurons that have their embryonic origin in the olfactory placode. We have observed that, besides their classical location, LHRH fibers can also be seen in the optic nerve and optic chiasm. Some LHRH fibers could also be traced in the optic tract. The possible course of these projections, and their functional significance are discussed.

Age Factors↗

Retinal ganglion cell axon progression from the optic chiasm to initiate optic tract development requires cell autonomous function of GAP-43.

Pathfinding mechanisms underlying retinal ganglion cell (RGC) axon growth from the optic chiasm into the optic tract are unknown. Previous work has shown that mouse embryos deficient in GAP-43 have an enlarged optic chiasm within which RGC axons were reportedly stalled. Here we have found that the enlarged chiasm of GAP-43 null mouse embryos appears subsequent to a failure of the earliest RGC axons to progress laterally through the chiasm-tract transition zone to form the optic tract. Previous work has shown that ventral diencephalon CD44/stage-specific embryonic antigen (SSEA) neurons provide guidance information for RGC axons during chiasm formation. Here we found that in the chiasm-tract transition zone, axons of CD44/SSEA neurons precede RGC axons into the lateral diencephalic wall and like RGC axons also express GAP-43. However unlike RGC axons, CD44/SSEA axon trajectories are unaffected in GAP-43 null embryos, indicating that GAP-43-dependent guidance at this site is RGC axon specific or occurs only at specific developmental times. To determine whether the phenotype results from loss of GAP-43 in RGCs or in diencephalon components such as CD44/SSEA axons, wild-type, heterozygous, or homozygous GAP-43 null donor retinal tissues were grafted onto host diencephalons of all three genotypes, and graft axon growth into the optic tract region was assessed. Results show that optic tract development requires cell autonomous GAP-43 function in RGC axons and not in cellular elements of the ventral diencephalon or transition zone.

Animals↗

Optic nerve regeneration after intravitreal peripheral nerve implants: trajectories of axons regrowing through the optic chiasm into the optic tracts.

We have studied axon regeneration through the optic chiasm of adult rats 30 days after prechiasmatic intracranial optic nerve crush and serial intravitreal sciatic nerve grafting on day 0 and 14 post-lesion. The experiments comprised three groups of treated rats and three groups of controls. All treated animals received intravitreal grafts either into the left eye after both left sided (unilateral) and bilateral optic nerve transection, or into both eyes after bilateral optic nerve transection. Control eyes were all sham grafted on day 0 and 14 post-lesion, and the optic nerves either unlesioned, or crushed unilaterally or bilaterally. No regeneration through the chiasm was seen in any of the lesioned control optic nerves. In all experimental groups, large numbers of axons regenerated across the optic nerve lesions ipsilateral to the grafted eyes, traversed the short distal segment of the optic nerve and invaded the chiasm without deflection. Regeneration was correlated with the absence of the mesodermal components in the scar. In all cases, axon regrowth through the chiasm appeared to establish a major crossed and a minor uncrossed projection into both optic tracts, with some aberrant growth into the contralateral optic nerve. Axons preferentially regenerated within the degenerating trajectories from their own eye, through fragmented myelin and axonal debris, and reactive astrocytes, oligodendrocytes, microglia and macrophages. In bilaterally lesioned animals, no regeneration was detected in the optic nerve of the unimplanted eye. Although astrocytes became reactive and their processes proliferated, the architecture of their intrafascicular processes was little perturbed after optic nerve transection within either the distal optic nerve segment or the chiasm. The re-establishment of a comparatively normal pattern of passage through the chiasm by regenerating axons in the adult might therefore be organised by this relatively immutable scaffold of astrocyte processes. Binocular interactions between regenerating axons from both nerves (after bilateral optic nerve transection and intravitreal grafting), and between regenerating axons and the intact transchiasmatic projections from the unlesioned eye (after unilateral optic nerve lesions and after ipsilateral grafting) may not be important in establishing the divergent trajectories, since regenerating axons behave similarly in the presence and absence of an intact projection from the other eye.

Age Factors↗

Studies on the optic chiasm of the leopard frog. II. Organization of retinotectal fibers in the optic chiasm.

The organization of retinotectal fibers in the optic chiasm was investigated using horseradish peroxidase (HRP) histochemistry and electrophysiological recording. HRP injection into a small region of the tectum led to retrograde staining of labeled fibers in a circumscribed region of the chiasm and staining of labeled ganglion cells in the contralateral retina. In each instance labeled tissue was spread over a greater proportion of the area of a chiasm section than over the flattened retina. Fibers originating in central (older) retina are located in dorsal chiasm. Fibers originating in peripheral (younger) retina are located in ventral chiasm. Viewed with the electron microscope, labeled unmyelinated fibers are admixed with labeled myelinated fibers. Neuronal activity was monitored with an extracellular microelectrode from points in dorsoventral tracks in the chiasm. Multiple units were recorded at each chiasm location. Using visual stimuli, the receptive fields of the units were mapped. The fields were distributed along an arc across the visual field. At ventral chiasm recording sites the arc was in the peripheral part of the visual field. In succeeding dorsal sites the arcs were concentrically arranged so that the more dorsal the chiasm recording site, the more central was the arc in the visual field. Thus, in the optic chiasm, retinal fibers appear to be organized chronotopically but not retinotopically. Fibers of the same age but from different locations in the retina are mixed together.

Animals↗

Studies on the optic chiasm of the leopard frog. I. Selective loss of visually elicited avoidance behavior after optic chiasm hemisection.

We hemisected either the posterior or anterior portion of the optic chiasm and found that frogs were unresponsive to large looming stimuli anywhere in the visual field. Nonetheless, the animals responded to prey stimuli throughout the visual field. Responses to looming stimuli returned in 1 to 8 weeks post-surgery. After complete transection of the chiasm animals were unresponsive to both prey and large looming stimuli. Frogs responded normally to prey and looming stimuli if less than half the optic chiasm was cut or if the postoptic commissure was cut. Since responses to looming stimuli returned before cut optic fibers could regenerate, these results suggest that visual information concerning prey and large looming objects are mediated by separate optic nerve fiber systems.

Animals↗