Search results for "Eye"

showing 10 items of 2511 documents

Influence of the gaze-stabilizing eye movements on the quality of the retinal image of the human eye

2000

In this work we have studied the influence of the gaze stabilizing movements of the eye on the quality of the retinal image of the human eye obtained by double pass methods. The results obtained agree with the expected differences between the coherent and incoherent behaviour of the optical system of the eye. The movements-free retinal image is obtained from a typical retinal image by considering a filter function in the frequency domain which characterizes the effect of the considered movements.

Retinagenetic structuresbusiness.industryImage qualityComputer scienceEye movementGazeeye diseasesAtomic and Molecular Physics and OpticsRetinal correspondenceOpticsmedicine.anatomical_structureFrequency domainmedicineEye trackingComputer visionHuman eyesense organsArtificial intelligencebusinessJournal of Modern Optics
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A novel murine model of aging of the human retina

2008

Purpose Accumulation of lipids, and especially of cholesteryl esters, under the retinal pigment epithelium and within Bruch’s membrane is a normal feature of aging and has also been observed in human eyes with age-related maculopathy. Our objective was to evaluate the retinal phenotype of apoB100,LDLR-/- mice, a model for lipid metabolism dysfunction and potentially of aging of the retina. Methods ApoB100,LDLR-/- mice were studied at 7 and 14 months of age by standard scotopic and photopic electroretinography by comparison to control animals. Fundus images were obtained with a confocal SLO (Heidelberg Retina Angiograph). The integrity of the vascular system was investigated by means of fluo…

Retinamedicine.medical_specialtyRetinal pigment epitheliumgenetic structuresLipid metabolismRetinalGeneral MedicineAnatomyFundus (eye)Biologymedicine.diseaseeye diseasesOphthalmologychemistry.chemical_compoundmedicine.anatomical_structurechemistryOphthalmologymedicineMaculopathylipids (amino acids peptides and proteins)sense organsScotopic visionPhotopic visionActa Ophthalmologica
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OPTICAL COHERENCE TOMOGRAPHIC FINDINGS IN BIETTI’S CRYSTALLINE TAPETORETINAL DYSTROPHY

2014

Purpose: To report the optical coherence tomography (OCT) findings of Bietti crystalline tapetoretinal dystrophy. Design: Observational case report. Methods: A subject with Bietti crystalline tapetoretinal dystrophy was evaluated with ophthalmoscopy, fluorescein angiography, and OCT (Stratus). Results: OCT showed thinning and hyporeflectivity of the outer nuclear layer in the macula due to photoreceptor degeneration. The retinal areas showing atrophy of the retinal pigment epithelium displayed greater penetration of the optical beam into the choroid and visualization of residual choroidal vessels. The hyperreflective band normally seen under the neurosensory retina was extremely wide when a…

Retinamedicine.medical_specialtyRetinal pigment epitheliumgenetic structuresmedicine.diagnostic_testbusiness.industryRetinalGeneral MedicineFluorescein angiographyeye diseasesOphthalmoscopyOphthalmologychemistry.chemical_compoundmedicine.anatomical_structureOptical coherence tomographychemistryOphthalmologymedicinesense organsChoroidbusinessOuter nuclear layerRETINAL Cases & Brief Reports
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Evidence of neuroplasticity in the human visual cortex following beneficial anti-VEGF treatment in exudative age-related macular degeneration

2012

Purpose Anti-vascular endothelial growth factor (VEGF) agents have been shown to improve visual acuity and prevent vision loss in exudative age-related macular degeneration (AMD). As the vision improves relatively quickly in response to intravitreal injections, we wanted to know whether this improvement is reflected in electrophysiolocal markers of visual cortical processing. Methods Our interventional case series included 6 elderly patients who underwent injection treatment to the affected eye. Their visual acuity, tomographic images of retinal thickness and visual evoked potentials (VEP) were assessed before of the treatment and six weeks after the last injection. Results All patients sho…

Retinamedicine.medical_specialtyVisual acuitygenetic structuresbusiness.industryRetinalGeneral MedicineMacular degenerationAudiologymedicine.diseaseExudative age-related macular degenerationeye diseasesOphthalmologychemistry.chemical_compoundmedicine.anatomical_structureVisual cortexchemistryOphthalmologyNeuroplasticityMedicinesense organsAnti vegf treatmentmedicine.symptombusinessActa Ophthalmologica
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Separate processing of “color” and “brightness” in goldfish

1991

Spectral sensitivity was measured under different adaptation levels using a behavioral training technique in which the fish had to discriminate between a dark test field and a test field illuminated with monochromatic light. Depending on which of the two test fields was used as training test field, two functions were obtained which differ (1) in absolute sensitivity and (2) in shape. When trained on the dark test field, the fish seems to discriminate on the basis of a "color" cue, but it uses a "brightness" cue when trained on the illuminated test field. This was concluded from measurements of wavelength discrimination. Under low levels of the adaptation light (1.5 and 0.2 lx instead of 20 …

Retinal Ganglion CellsBrightnessLightgenetic structuresField (physics)Color visionDark AdaptationAdaptation (eye)OpticsGoldfishPsychophysicsPsychophysicsAnimalsPhotoreceptor CellsVisual Pathwaysbusiness.industrySensory SystemsElectrophysiologyOphthalmologySpectral sensitivitySensory Thresholdssense organsMonochromatic colorPsychologybusinessSensitivity (electronics)Color PerceptionVision Research
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A new vicious cycle involving glutamate excitotoxicity, oxidative stress and mitochondrial dynamics

2011

Glutamate excitotoxicity leads to fragmented mitochondria in neurodegenerative diseases, mediated by nitric oxide and S-nitrosylation of dynamin-related protein 1, a mitochondrial outer membrane fission protein. Optic atrophy gene 1 (OPA1) is an inner membrane protein important for mitochondrial fusion. Autosomal dominant optic atrophy (ADOA), caused by mutations in OPA1, is a neurodegenerative disease affecting mainly retinal ganglion cells (RGCs). Here, we showed that OPA1 deficiency in an ADOA model influences N-methyl-D-aspartate (NMDA) receptor expression, which is involved in glutamate excitotoxicity and oxidative stress. Opa1enu/+mice show a slow progressive loss of RGCs, activation …

Retinal Ganglion CellsCancer ResearchReceptor expressionExcitotoxicityApoptosisNeurodegenerativeMitochondrionEyemedicine.disease_causeGTP PhosphohydrolasesMice0302 clinical medicineReceptorsoxidative stressPhosphorylationbcl-2-Associated X Protein0303 health sciencesbiologyGlutamate receptorMitochondriaUp-RegulationCell biologymitochondrial fusionAutosomal DominantOriginal Articlebcl-Associated Death ProteinMitochondrial fissionN-Methyl-D-AspartateBiotechnologymitochondrial fragmentationOncology and CarcinogenesisImmunologybcl-X ProteinSOD2Glutamic AcidReceptors N-Methyl-D-AspartateNMDA receptorsCell Line03 medical and health sciencesCellular and Molecular NeuroscienceBcl-2-associated X proteinOptic Atrophy Autosomal DominantmedicineAnimalsEye Disease and Disorders of Vision030304 developmental biologySuperoxide DismutaseNeurosciencesCell BiologyMolecular biologyeye diseasesOxidative StressOptic AtrophyMutationbiology.proteinOPA1 mutationBiochemistry and Cell Biologysense organsglutamate excitotoxicity030217 neurology & neurosurgeryCell Death & Disease
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Preclinical Retinal Neurodegeneration in a Model of Multiple Sclerosis

2012

Neurodegeneration plays a major role in multiple sclerosis (MS), in which it is thought to be the main determinant of permanent disability. However, the relationship between the immune response and the onset of neurodegeneration is still a matter of debate. Moreover, recent findings in MS patients raised the question of whether primary neurodegenerative changes can occur in the retina independent of optic nerve inflammation. Using a rat model of MS that frequently leads to optic neuritis, we have investigated the interconnection between neurodegenerative and inflammatory changes in the retina and the optic nerves with special focus on preclinical disease stages. We report that, before manif…

Retinal Ganglion CellsPathologyTime FactorsStilbamidinesgenetic structuresJournal ClubFreund's Adjuvantchemistry.chemical_compoundBlood-Retinal BarrierStudent’s SectionCell DeathMicrogliabiologyGeneral NeuroscienceRetinal DegenerationNeurodegenerationArticlesmedicine.anatomical_structureSpinal CordRetinal ganglion cellOptic nerveFemaleMicrogliaMyelin Proteinsmedicine.medical_specialtyMultiple SclerosisEnzyme-Linked Immunosorbent AssayRetinaMyelin oligodendrocyte glycoproteinMicroscopy Electron TransmissionAntigens CDOccludinGlial Fibrillary Acidic ProteinIn Situ Nick-End LabelingmedicineAnimalsOptic neuritisAquaporin 4Retinabusiness.industryMacrophagesMultiple sclerosisMembrane ProteinsRetinalOptic Nervemedicine.diseaseeye diseasesRatsDisease Models Animalchemistrybiology.proteinMyelin-Oligodendrocyte Glycoproteinsense organsbusinessNeuroscienceThe Journal of Neuroscience
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Ultrastructural study of the retina in late infantile metachromatic leukodystrophy.

1992

The autopsy of a 2-year-old girl revealed a clinically unrecognized metachromatic leukodystrophy (MLD) due to an aryl-sulfatase A deficiency, characteristically affecting the central and peripheral nervous system by demyelination and by accumulation of metachromatic material. The retina though reported clinically as normal, showed the same demyelinating process in the optic nerve including the papilla but an additional intraneuronal storage of MLD-typical lysosomal residual bodies in ganglion cell perikarya of the retina. Cells of the bipolar and photoreceptor layers as well as pigment epithelial cells were not affected by MLD-specific lysosomal storage. Thus, sulfatides seem to play a part…

Retinal Ganglion CellsPathologymedicine.medical_specialtyAutopsyBiologycomplex mixturesRetinaCellular and Molecular NeuroscienceRetinal DiseasesmedicineHumansRetinaBrainGeneral MedicineLeukodystrophy Metachromaticmedicine.diseaseeye diseasesSensory SystemsGanglionMajor duodenal papillaMetachromatic leukodystrophyOphthalmologymedicine.anatomical_structurePeripheral nervous systemChild PreschoolOptic nerveUltrastructureFemalesense organsLysosomesOphthalmic research
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Enrichment of Retinal Ganglion Cells in Rat Retinal Lysate by Excimer Laser Ablation of the Outer Retina

2013

PURPOSE. Retinal ganglion cells (RGC) are a relatively small cell population in the retina. This leads to an unfavorable signal-tonoise ratio when analyzing RGC proteins in whole retina lysate. We present a novel technique to obtain RGC-enriched rat retinal lysate by removing the outer retinal layers with an excimer laser before lysation. METHODS. Outer retinal layers were ablated with an excimer laser on flat mounted retinas from adult albino rats. 4 0 6Diamidino-2-phenylindole dihydrochloride hydrate (DAPI) nuclear staining was used to assess the ablation efficacy (n ! 6). Western blot for layer specific markers (rhodopsin, parvalbumin, b-III-tubulin) was performed to quantify changes in …

Retinal Ganglion CellsRhodopsingenetic structuresBlotting WesternPopulationRetinal ganglionRetina03 medical and health scienceschemistry.chemical_compound0302 clinical medicineTubulinmedicineAnimalseducationGanglion cell layerRetinaeducation.field_of_studyLaser ablationbiologyRetinalAnatomyCREB-Binding ProteinMolecular biologyeye diseasesRatsmedicine.anatomical_structurechemistryRhodopsin030221 ophthalmology & optometrybiology.proteinOptic nerveThy-1 AntigensLaser Therapysense organs030217 neurology & neurosurgeryInvestigative Opthalmology & Visual Science
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p27Kip1participates in the regulation of endoreplication in differentiating chick retinal ganglion cells

2015

Nuclear DNA duplication in the absence of cell division (i.e. endoreplication) leads to somatic polyploidy in eukaryotic cells. In contrast to some invertebrate neurons, whose nuclei may contain up to 200,000-fold the normal haploid DNA amount (C), polyploid neurons in higher vertebrates show only 4C DNA content. To explore the mechanism that prevents extra rounds of DNA synthesis in these latter cells we focused on the chick retina, where a population of tetraploid retinal ganglion cells (RGCs) has been described. We show that differentiating chick RGCs that express the neurotrophic receptors p75 and TrkB while lacking retinoblastoma protein, a feature of tetraploid RGCs, also express p27K…

Retinal Ganglion CellsretinaEndocycleCell divisionCellular differentiationChick EmbryoRetinoblastoma ProteinendoreduplicationMicevertebrateRNA Small InterferingpolyploidyMice KnockoutRGCeducation.field_of_studyCell DifferentiationEndoreduplicationCell cycleImmunohistochemistryNuclear DNAendocycleneurogenesiscell cycleRNA InterferenceCyclin-Dependent Kinase Inhibitor p27NeurogenesisPopulationDown-RegulationCell cycleBiologyRetinal ganglionRetinaPolyploidyReportAnimalsReceptor trkBEndoreduplicationeducationMolecular BiologyPloidiesDNA synthesisVertebrateCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cell BiologyMinichromosome Maintenance Complex Component 7Molecular biologyeye diseasessense organsChickensDevelopmental BiologyCell Cycle
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