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Evidence for transient forces/strains at the optic nerve head in myopia: repeated measurements of the Stiles-Crawford effect of the first kind (SCE-I) over time.

Probable transient changes in photoreceptor alignments, inferred from the measurements of the Stiles-Crawford effect of the first kind (SCE - I), were demonstrated in myopic eyes with elongated axial length (regardless of the magnitude of refractive error) at three retinal locations; the fovea (point of fixation), and 22 degrees and 27 degrees in the nasal retina. The changes were much bigger at 22 degrees and 27 degrees in the nasal retina (which are located beyond the optic nerve head) than at the fovea. These transient effects were revealed by repeatedly testing the same retinal locations over a period of time. Time intervals between the subsequent/repeated measurements ranged from less than an hour to several months. In some locations, the changes were recorded in less than an hour. Collectively, these were very meaningful changes. Generally bigger effects were recorded in the horizontal SCE - I than in the vertical SCE - I.

Fovea Centralis↗

Immunocytochemical characterisation of proteins secreted by retinal pigment epithelium in retinas of normal and Royal College of Surgeons dystrophic rats.

In a previous study, an antigen consisting of proteins secreted by retinal pigment epithelial (RPE) cells was injected into a sheep and the specificity of the resulting antiserum was shown by Western blotting and its effects on retinal development were determined in vitro and in vivo. In the present study, the distribution of these secreted proteins was determined by light microscopy immunocytochemistry in cultured neonatal rat RPE cells and retinas of normal and Royal College of Surgeons (RCS) dystrophic rats and cerebrum of normal adult rats. Immunolabelling for these RPE-secreted proteins was detected in cytoplasmic vesicles surrounding nuclei and within processes of cultured normal and transformed rat RPE. In retinas of late postnatal and adult rats, dense immunostaining was found in the cytoplasm of RPE cells and ganglion cell bodies. In addition to RPE and ganglion cells, scattered photoreceptors within the thin outer nuclear layer and small structures within the debris zone were also densely immunoreactive in retinas of 2-mo-old RCS dystrophic rats. The numbers of immunostained ganglion cells appeared to decrease in retinas of older RCS rats, although the immunoreactivity within the RPE appeared to increase in density. No other neuron within the retina, i.e. bipolar, amacrine or horizontal, was immunoreactive for RPE-secreted proteins. In the cerebral cortex of adult rats, immunoreactivity for RPE-secreted proteins was primarily detected within large perikarya of pyramidal neurons and smaller granule neurons. In conclusion, we report an immunocytochemical analysis of an antiserum raised against secreted proteins of rat RPE. This antiserum recognised proteins within secretory-like vesicles of cultured neonatal normal and transformed rat RPE and showed a specificity for RPE and ganglion cells in normal rat retinas, that appeared to be developmentally regulated, and neuron perikarya in adult rat cerebrum.

Animals↗

The pretectal nucleus lentiformis mesencephali of Rana pipiens.

The pretectal nucleus lentiformis mesencephali (nLM) of Rana pipiens was investigated with autoradiographic, horseradish peroxidase (HRP), and Golgi techniques. Retinal afferents to nLM originate primarily from the central retina. The primary projection is contralateral with a small ipsilateral component. Following optic nerve transection and HRP impregnation, contralateral retinal afferents show a restricted, dense core of HRP label in the superficial portion of the nucleus with sparser HRP label in the surround. Ipsilateral retinal afferents arborize throughout nLM, except in the dense-core region. Additional afferents to nLM originate from the ipsilateral tectum, the nucleus rotundus, the mesencephalic pretectal gray, the contralateral nLM, and the nucleus of the basal optic root. Afferents from the accessory optic system arborize only in the dense-core region, following HRP injections into the nucleus of the basal optic root, while afferents from the mesencephalic pretectal gray arborize in all parts of nLM except the dense core. Afferents from the tectum and anterior thalamus appear to arborize throughout the nucleus without discernible pattern. The lamination of afferent terminals in nLM was correlated with Nissl-stained cytoarchitectural material in which the majority of large neurons cluster around the dense core of nLM. Three types of neurons occur in nLM: large neurons (25-micron dia.), fusiform neurons (12.5-micron dia.), and stellate neurons (10-micron dia.). Additionally, two cell groups outside nLM which send dendrites into the nucleus were observed: cells of the posterior lateral nucleus and cells of the posterior thalamic pretectal gray. Both large and fusiform neurons project to the deep layers of the optic tectum as well as to the ventral rhombencephalon superficial to the abducens nucleus. While a small number of fusiform neurons project to the nucleus of the basal optic root, the stellate neurons appear to be intrinsic to nLM. The anuran nLM strongly resembles the nucleus of the optic tract in mammals in terms of the site of origin of its retinal afferents, lamination of afferent terminations, its central connections, and its demonstrated involvement in horizontal optokinetic nystagmus.

Animals↗

Uniqueness of the S-cone pedicle in the human retina and consequences for color processing.

The purpose of this study was to investigate more fully the shape and content of ribbons and synapses to second-order neurons in the short-wavelength cone (S-cone, blue cone) pedicle and to learn more concerning the uniqueness of the S-cone system in the primate retina. A piece of well-fixed peripheral human retina (10 mm, 35 degrees nasal to the fovea) was serially thick sectioned in the tangential plane from the level of the outer segments to the tops of the cone pedicles. Then serial electron microscope (EM) sections were collected through the whole depth of the pedicle-occupying region into the neuropil of the outer plexiform layer (OPL). The resultant EM micrograph montages of a large field of cone pedicles were perused, and S-cone pedicles were identified. Serial micrographs of a single S-cone pedicle, picked out of the montages, were digitized and reconstructed by computer three-dimensional methods. The S-cone pedicle arose from a slightly oblique axon and projected 0.5-1 microm more vitread in the OPL than other cone pedicles. It was bilobed in shape, with synaptic invaginations and ribbons in both lobes. No cone-contacting telodendria projected from the S-cone pedicle itself, but a small number of neighboring cones sent telodendria to its surface to make small gap junctions. Neighboring rod spherules also made small gap junctions. Four robust bipolar cell dendrites, most likely from S-cone-specific bipolar cells, made synapses at ribbons and basal (distal) junctions. A small number of other bipolar cell dendrites made narrow-cleft basal junction only. The majority of lateral elements were thought to be from HII horizontal cells, and a minority from HI horizontal cells. We conclude that the S-cone pedicle has a unique morphology and connectivity to second-order neurons that makes it quite different from the other two longer wavelength cone systems, and we speculate on the consequences for color processing in the visual system in general.

Adult↗

Photoreceptors, visual pigments, and ellipsosomes in the killifish, Fundulus heteroclitus: a microspectrophotometric and histological study.

The photoreceptor layer of F. heteroclitus was examined by light and electron microscopy. We identified four cone visual pigments with maximum absorbance (lambda(max)) in the UV (363 nm), short (400 nm), middle (463 nm), and long (563 nm) wavelength regions of the spectrum and a rod visual pigment that peaked in the middle wavelengths (503 nm). Electron-dense bodies, ellipsosomes and pseudoellipsosomes, were present in the distal ellipsoids of long/middle (L/M) and long/long (L/L) wavelength double cones and in single short wavelength (S) cones, respectively. The light absorption of ellipsosomes indicated the presence of reduced cytochrome-c with the highest optical densities found in the M members of L/M double cones. By contrast, S cones contained pseudo-ellipsosomes which had very low optical density. UV cones were present everywhere as part of square or row mosaics in the retina of F. heteroclitus. Cone packing was on average higher for locations in the upper half of the retina while the highest cone density was found in the centro-ventral retina. An analysis of potential quantum catches for each cone type as a function of retinal sector and underwater irradiance characteristics revealed higher overall quantum catches for cones in the upper retina when the light field was assumed homogeneous, and higher quantum catches for cones in the lower retina when downwelling, horizontal, and upwelling irradiances were considered separately. At dusk, quantum catch was highest for M cones and the contribution to the overall retinal quantum catch by UV and S cones was much greater than during daylight hours. We propose that UV and S cones may be used to detect targets of interest against the background irradiance sensed by double cones.

Animals↗

Spatial and temporal properties of interocular timing differences in multifocal visual evoked potentials.

The multifocal VEPs (mfVEPs) obtained from the right and left eyes are practically identical in shape and amplitude, however small differences in the implicit times (ITs) have been reported. We have analyzed the ITs in detail to show that they are dependent on the radial location of the stimulus in the visual field. The differences are large, up to 8.3 ms, near the horizontal meridian, and are probably due to differences in the distances of the nasal and temporal ganglion cell axons from the optic disc. The intraretinal conduction velocity of ganglion cell axons, determined by dividing the axonal length to the optic disc by the ITs, was 0.29 m/s at an eccentricity of 0.5-1.4 degrees and 1.39 m/s at 8-12 degrees .

Adult↗

End-stopped cells and binocular depth discrimination in the striate cortex of cats.

Proposals concerning neural mechanisms for binocular depth discrimination have been criticized on the grounds that only striate cells with a preferred stimulus orientation not too far from the vertical can make significant horizontal disparity discriminations. We investigated this claim by preparing a two-dimensional array of position-disparity response profiles to moving light and dark bars from each of 18 cells in the simple family. From these arrays, it was possible to reconstruct disparity response profiles along any axis across the receptive field, irrespective of the cell's optimal stimulus orientation. This analysis showed that cells with a predominantly excitatory binocular response (N = 10) can make precise horizontal disparity discriminations, independent of their optimal stimulus orientation, provided that they are sufficiently end stopped. End-free cells, on the other hand, are effective for horizontal disparity discriminations only if their preferred orientation are near the vertical. Nearly all striate cells we examined were end-stopped to some degree and nearly half had an end inhibition sufficient to reduce the monocular response from the dominant eye to half its maximal amplitude. Cells having a predominantly inhibitory disparity response profile of the symmetric type (N = 8) have an inhibitory profile along every axis across the receptive field. An outline is given of a neural mechanism for the determination of absolute viewing distance based on the sensitivities of striate cells to vertical retinal-image disparities.

Animals↗

Retinal organisation in a hill-stream cyprinid, Crossocheilus latius latius Hamilton.

The retinal organisation of a cyprinid fish, Crossocheilus latius latius Hamilton, which inhabits the sub-Himalayan torrents of Sikkim, India, has been studied by light microscopy. The fish are small and cylindrical having relatively large eyes with a large, oval pupil. They are adapted to the low-light level of the hill-torrents, which is caused by the heavily silted monsoon water. The retina possesses numerous rods and bulky cones, the latter containing multiple oil droplets, and located mostly sclerally and some both sclerally and vitreally. There are three rows of large horizontal cells and a few bipolar and sparsely distributed ganglion cells. Retinomotor response, as evidenced by the scleral migrations of photoreceptors and pigment epithelium during dark-adaptation, is prominent in the species. The bulky cones with their prominent, multiple oil droplets have been suggested as the devices which help the fish to negotiate in the hill-stream's turbid environment.

Animals↗

Horizontal cells in the retina of the rabbit.

The light responses, morphology, and connections of horizontal cells (HCs) were studied in the retina of the rabbit using intracellular recordings and the injection of visible markers. Two types of HCs were identified, axonless and axon-bearing HCs. Axonless HCs and the somatic end of axon-bearing HCs respond to white light of varying intensity with graded hyperpolarizations; both display a transient superimposed on the sustained hyperpolarization at stimulus initiation and a small rod aftereffect at the cessation of high intensity stimuli. Anatomically, both are connected to cones, but their responses also suggest rod influence. Both summate stimuli from a retinal area which is much larger than their respective fields. However, only axonless HCs transfer a fluorescent, low molecular weight dye to adjoining, homologous cells. The axon terminal of axon-bearing HCs has response properties different from those of the cell body: the transient at stimulus initiation is absent; furthermore, at high levels of illumination, the rod aftereffect becomes equal in amplitude to the primary hyperpolarization. Anatomically, it is connected to rods, but its responses also suggest cone influence. Its receptive field approximates in diameter its anatomical spread and it does not transfer fluorescent dye to its neighbors.

Animals↗

Histology of the ferret retina.

The retina of the adult ferret, Mustelo furo, was studied with light and transmission electron microscopy to provide an anatomical basis for use of the ferret as a model for retinal research. The pigment epithelium is a simple cuboidal layer of cells characterized by a zone of basal folds, apical microvilli, and pigment granules at various stages of maturation. The distinction between rod and cone photoreceptor cells is based on their location, morphology, heterochromatin pattern and the electron density of their inner segments. The round, light-staining cone cell nuclei occupy the layer of perikarya along the apical border of the outer nuclear layer. The remainder of the outer nuclear layer consists of oblong, deeply-stained rod cell nuclei. Ribbon type synaptic complexes involving photoreceptor cell axons, horizontal cell processes, and bipolar cell dendrites characterize the outer plexiform layer. The inner nuclear layer is comprised of horizontal, bipolar, and amacrine cell perikarya as well as the perikarya of the Müller cells. The light-staining horizontal cell nuclei are prominent along the apical border of the inner nuclear layer. The light-staining amacrine cell nuclei form a more or less continuous layer along the basal border of the inner nuclear layer. Both conventional and ribbon-type synapses characterize the inner plexiform layer. The ganglion cells form a single cell layer. The optic fiber layer contains bundles of axons surrounded by Müller cell processes. Small blood vessels and capillaries are present in the basal portion of the retina throughout the region extending from the internal limiting membrane to the outer plexiform layer. The adult one-year-old retina is compared with the retina at the time of eye opening.

Animals↗

Postnatal development of somatostatin 2A (sst2A) receptors expression in the rabbit retina.

In the retina, somatostatin (SRIF) acts as a neuromodulator by interacting with specific SRIF subtype (sst) receptors. Aim of this investigation was to determine the cellular localization of the sst2A receptor isoform in the postnatal rabbit retina. Receptor immunoreactivity was localized using the antiserum K-230, directed to the C-terminus of the human sst2A receptor. In the postnatal rabbit retina, sst2A receptors were abundantly expressed without significant regional differences. They were localized predominantly to rod bipolar cells, identified with a protein kinase C (PKC) antibody, to amacrine cells, some of which also containing tyrosine hydroxylase (TH), and to presumed rare horizontal cells. Quantitative analysis showed that sst2A-immunoreactive (-IR) bipolar and amacrine cells reached their maximum density and absolute number at the time of eye opening, when the expression pattern of sst2A receptors was similar to that in adult retinas. In the adult retina, 68% of the PKC-IR rod bipolars and 34% of the TH-IR amacrine cells were observed to also express sst2A receptors. The appearance of sst2A receptor immunolabeling prior to eye opening and the developmental profile of sst2A receptor expression are compatible with a role of SRIF in the maturation of retinal circuitries. The partial expression of sst2A receptors in PKC-IR rod bipolar cells and in TH-IR amacrine cells may suggest some type of heterogeneity within these cell populations.

Animals↗

Immunocytochemical identification of cone bipolar cells in the rat retina.

We studied the morphology of bipolar cells in fixed vertical tissue sections of the rat retina by injecting the cells with Lucifer Yellow and neurobiotin. In addition to the rod bipolar cell, nine different putative cone bipolar cell types were distinguished according to the position of their somata in the inner nuclear layer and the branching pattern and stratification level of their axon terminals in the inner plexiform layer. Some of these bipolar cell populations were labeled immunocytochemically in vertical and horizontal sections using antibodies against the calcium-binding protein recoverin, the glutamate transporter GLT-1, the alpha isoform of the protein kinase C, and the Purkinje cell marker L7. These immunocytochemically labeled cell types were characterized in terms of cell density and distribution. We found that rod bipolar cells and GLT-1-positive cone bipolar cells occur at higher densities in a small region located in the upper central retina. This area probably corresponds to the central area, which is the region of highest ganglion cell density. A second peak of rod bipolar cell density in the lower temporal periphery matches the retinal area of binocular overlap. The population densities of the immunocytochemically characterized bipolar cells indicate that at least 50% of all bipolar cells are cone bipolar cells. The variety and total number of cone bipolar cells is surprising because the retina of the rat contains 99% rods. Our findings suggest that cone bipolar cells may play a more important role in the visual system of the rat than previously thought.

Animals↗

Dopamine modifies the balance of rod and cone inputs to horizontal cells of the Xenopus retina.

Dopamine (greater than or equal to 2 microM) increased the cone input and suppressed the rod input to axon-bearing horizontal cells of the Xenopus retina. Dopamine (10 microM) also depolarized the horizontal cell by about 9 mV. The D2-dopamine antagonists spiperone and metoclopramide had the opposite action to dopamine, whereas the D1-dopamine antagonist SCH 23390 was without effect. None of the agents tested modified the light-evoked responses of rods.

Animals↗

[Experimental studies on lesions of eye tissues in cobalt intoxication].

The aim of the paper was to examine the influence of cobalt compound on rabbit eye tissues. The lesions in the eyeball were evaluated basing on ophthalmological examination and in light and electron microscopes. The studies revealed that cobalt intoxication caused the following damages in the rabbit retina: oedema and atrophy of nerve fibres, lesions of ganglion, amacrine, bipolar, horizontal cells and nucleus of photoreceptors. Also, obliteration of choroidal vessels and changes in iris and ciliary body were found. Cataract developed in 42% of rabbits and 25% chronic purulent endophthalmitis in 25%. The results of these experimental investigations indicate that further studies on the influence of this metal on human eye tissues are necessary.

Animals↗

Cytogenesis in the monkey retina.

Time of cell origin in the retina of the rhesus monkey (Macaca mulatta) was studied by plotting the number of heavily radiolabeled nuclei in autoradiograms prepared from 2- to 6-month-old animals, each of which was exposed to a pulse of 3H-thymidine (3H-TdR) on a single embryonic (E) or postnatal (P) day. Cell birth in the monkey retina begins just after E27, and approximately 96% of cells are generated by E120. The remaining cells are produced during the last (approximately 45) prenatal days and into the first several weeks after birth. Cell genesis begins near the fovea, and proceeds towards the periphery. Cell division largely ceases in the foveal and perifoveal regions by E56. Despite extensive overlap, a class-specific sequence of cell birth was observed. Ganglion and horizontal cells, which are born first, have largely congruent periods of cell genesis with the peak between E38 and E43, and termination around E70. The first labeled cones were apparent by E33, and their highest density was achieved between E43 and E56, tapering to low values at E70, although some cones are generated in the far periphery as late as E110. Amacrine cells are next in the cell birth sequence and begin genesis at E43, reach a peak production between E56 and E85, and cease by E110. Bipolar cell birth begins at the same time as amacrines, but appears to be separate from them temporally since their production reaches a peak between E56 and E102, and persists beyond the day of birth. Müller cells and rod photoreceptors, which begin to be generated at E45, achieve a peak, and decrease in density at the same time as bipolar cells, but continue genesis at low density on the day of birth. Thus, bipolar, Müller, and rod cells have a similar time of origin. The maximal temporal separation of cell birth is between cones and amacrine cells so that cell generation exhibits two relatively distinct phases: the first phase gives rise to ganglion, horizontal, and cone cells, and the second phase to amacrine, bipolar, rod, and Müller cells. In addition, cells of the first phase are generated faster than the second phase cells, and there are differences in the topography of spread of labeled cells between the two phases. Each cell class displays a central-to-peripheral gradient in genesis, although the spatiotemporal characteristics of the gradients differ between the classes.(ABSTRACT TRUNCATED AT 400 WORDS)

Aging↗

Retinal GABA neurons: localization in vertebrate species using an antiserum to rabbit brain glutamate decarboxylase.

Retinal gamma-aminobutyric acid (GABA) neurons have been localized immunocytochemically using a new antiserum against rabbit brain glutamate decarboxylase (GAD). The animals examined were: dogfish, ratfish, goldfish, catfish, turtle, chick, mouse, rat, pig, rabbit, cat and New World monkey. GAD-containing processes, observed as punctate deposits of immunochemical reaction product, formed discrete bands within the inner plexiform layers of all retinas examined. Immunoreactive, and therefore presumably GABAergic, amacrine cells were observed in all species. Displaced GABAergic amacrine cells were observed in the retinas of goldfish, catfish, turtle and chick, and sparsely in the rabbit as well. GABAergic horizontal cells were detected in catfish, goldfish, chick and turtle. Interplexiform cells in the cat and the rat were clearly immunoreactive for glutamate decarboxylase; this is the first report of GABAergic interplexiform cells in the rat.

Animals↗

Soluble guanylate cyclase and nitric oxide synthase in synaptosomal fractions of bovine retina.

Cyclic GMP has been shown in recent years to directly activate ion channels in bipolar and ganglion cells, and to indirectly regulate coupling between horizontal cells, and between bipolar and amacrine cells. In all of these cases, the effects of cyclic GMP are mimicked by nitric oxide. An increase in calcium concentration stimulates the production of nitric oxide by neuronal and endothelial forms of nitric oxide synthase, which in turn activates soluble guanylate cyclases, enhancing the synthesis of cyclic GMP. Though some effects of nitric oxide do not involve cyclic GMP, the nitric oxide-cyclic GMP cascade is well recognized as a signaling mechanism in brain and other tissues. The widespread occurrence of nitric oxide/cyclic GMP-regulated ion channel activity in retinal neurons raises the possibility that nitric-oxide-sensitive soluble guanylate cyclases play an important role in cell-cell communication, and possibly, synaptic transmission. Immunohistochemical studies have indicated the presence of soluble guanylate cyclase in retinal synaptic layers, but such studies are not suitable for determination of the density or quantitative subcellular distribution of the enzyme. Microanalytical methods involving microdissection of frozen retina also showed the presence of cyclase activity in retinal plexiform layers but these methods did not permit distinction between nitric oxide-sensitive and insensitive cyclases. In this study, we fractionated retinal homogenate into the cytosolic and synaptosomal fractions and investigated the specific activity and distribution of soluble guanylate cyclase and nitric oxide synthase. The results show that both enzymes are present in the synaptosomal fractions derived from inner and outer plexiform layers. The synaptosomal fraction derived from inner retina was highly enriched in cyclase activity. Nitric oxide synthase activity was also higher in the inner than outer retinal synaptosomal fraction. The results suggest that the nitric oxide-cyclic GMP system is operational in both synaptic layers of retina and that it may play a more significant role in the inner retina.

Animals↗

Transient adaptation and sensitization in the retina of Necturus.

Responses to repetitive stimulation were monitored at several retinal levels in the eyecup of the mudpuppy Necturus maculosus. When alternating sequences of low-intensity small and large spots were presented, two effects were found, which could be localized to the proximal retina: (a) response decrement (RD), in which, after the first small spot response, subsequent small spot responses are decreased in amplitude and (b) transient response enhancement (TRE), in which the first small spot response after a large spot sequence is larger than preceding or subsequent small spot responses. RD and TRE are absent or weak in sustained on or off responses (horizontal and bipolar cells, and ON and OFF ganglion cell post-stimulus time histograms (PSTH) but are particularly well developed in the on/off responses of the proximal retina (proximal negative response, M-wave, PSTHs of ON/OFF ganglion cells, and intracellular responses from on/off neurons and Müller cells). RD and TRE appear to arise from a stimulus-evoked slow depolarization in on/off neurons that interacts with the amplitude of succeeding responses. We conclude that RD and TRE are a form of neural adaptation that is largely specific to the on/off channels of the proximal retina.

Action Potentials↗