Search results for "Retinal"

showing 10 items of 631 documents

An ultrastructural study on retinal neural and pigment epithelial cells in ovine neuronal ceroid-lipofuscinosis.

1990

Ovine neuronal ceroid-lipofuscinosis represents another well studied model for human neuronal ceroid-lipofuscinosis (NCL). Accumulation of abnormal lipopigments in various retinal neurons, and loss of photoreceptors are similar to the lesions in human juvenile NCL and indicate that the sheep is a suitable model in which to study the pathogenesis of both NCL lipopigment formation and retinopathia pigmentosa. However, this latter process is not as advanced in NCL-diseased sheep as in human patients but far more obvious than in canine NCL in which retinopathy cannot be unequivocally documented. Ovine NCL shares with canine NCL peculiar lamellar inclusions in retinal pigment epithelial cells wh…

Pathologymedicine.medical_specialtySheep DiseasesBiologyRetinaLipofuscinPathogenesischemistry.chemical_compoundPigmentNeuronal Ceroid-LipofuscinosesmedicineAnimalsPhotoreceptor CellsPigment Epithelium of EyeGenetics (clinical)SheepCatabolismRetinalmedicine.diseaseCell biologyOphthalmologychemistryvisual_artPediatrics Perinatology and Child HealthUltrastructurevisual_art.visual_art_mediumNeuronal ceroid lipofuscinosissense organsRetinopathyOphthalmic paediatrics and genetics
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AN ULTRASTRUCTURAL STUDY OF THE RETINA IN HUMAN LATE INFANTILE NEUROAXONAL DYSTROPHY

1993

A case involving a girl who died at 11 years of age and who had developed normally until the age of 18 months, at which time further psychomotor maturation stopped and then regressed, is reported. The patient appeared hypotonic and showed loss of deep tendon reflexes, as well as bulbar signs and increasing immobility. Visual impairment resulted in blindness at the age of 7 years. Her disease was diagnosed as late infantile neuroaxonal dystrophy (LINAD) after examination of sural nerve biopsy samples and after autopsy. Under electron microscopy, retinal axons were filled with tubulocisternal profiles and occasional large lamellar clefts close to or distant from synaptic complexes. These lesi…

Pathologymedicine.medical_specialtySural nerveAutopsyRetinaInfantile neuroaxonal dystrophychemistry.chemical_compoundRetinal DiseasesSural NerveHumansMedicineChildOuter nuclear layerMedulla OblongataRetinabusiness.industryMusclesRetinalHypertrophyGeneral Medicinemedicine.diseaseAxonsOphthalmologymedicine.anatomical_structurechemistryNerve DegenerationUltrastructureMedulla oblongataFemaleNervous System DiseasesbusinessRetina
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Norrie gene product is necessary for regression of hyaloid vessels.

2004

To investigate the nature and origin of the vitreous membranes in mice with knock-out of the Norrie gene product (ND mice).Eighty-two eyes of ND mice of different age groups (postnatal day [P]0-13 months) and 95 age-matched wild-type control mice were investigated. In vitreoretinal wholemounts and in sagittal sections, vessels and free cells were visualized by labeling for lectin. In addition, staining with a marker for macrophages (F4/80) and collagen XVIII/endostatin known to be involved in regression of hyaloid vessels was performed for light and electron microscopic investigations. Endostatin expression was confirmed by Western blot analysis.Wild-type controls showed the typical pattern…

Pathologymedicine.medical_specialtygenetic structuresAngiogenesisBlotting WesternNerve Tissue ProteinsBiologyRetinal NeovascularizationBlindnessGene productchemistry.chemical_compoundMiceVasculogenesismedicineAnimalsEye AbnormalitiesEye ProteinsMicroscopy ImmunoelectronMice KnockoutMembranesRetinal DegenerationRetinal VesselsRetinalGenetic Diseases X-LinkedAnatomyAntigens Differentiationeye diseasesEndostatinsVitreous Bodymedicine.anatomical_structurechemistryCirculatory systemcardiovascular systemsense organsEndostatinBlood vesselInvestigative ophthalmologyvisual science
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Ultrastructural study of primary canine and human pigmentary retinopathy

1985

An electron microscopic study was performed on eyes of Labrador dogs afflicted with progressive retinal atrophy (PRA). There was complete loss of photoreceptors, atrophy of the remaining retina and gliosis in the peripheral part while the central retina showed incomplete loss of photoreceptors and an almost total disappearance of photoreceptor outer segments. Melanin-bearing cells, largely containing melanolysosomes, were found deep inside the retina. This electron microscopic study also incorporated the retina of a middle-aged woman affected by retinopathia pigmentosa (RP). The fine structure of the diseased retina showed a similar pattern of lesions, more pronounced in the periphery of th…

Pathologymedicine.medical_specialtygenetic structuresBiologyRetinalaw.inventionDogsAtrophySpecies SpecificitylawRetinitis pigmentosamedicineAnimalsHumansDog DiseasesGenetics (clinical)Progressive retinal atrophyRetinaPigmentary RetinopathyMiddle Agedmedicine.diseaseeye diseasesOphthalmologymedicine.anatomical_structureGliosisPediatrics Perinatology and Child HealthUltrastructureFemalesense organsAtrophyElectron microscopemedicine.symptomRetinitis PigmentosaOphthalmic Paediatrics and Genetics
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Correlation Between Ischemic Retinal Accidents and Radial Peripapillary Capillaries in the Optic Nerve Using Optical Coherence Tomographic Angiograph…

2017

Background: Perfusion of the optic nerve has been widely studied using fluorescein angiography (FAG), which is currently regarded as the criterion standard. However, FAG has adverse effects associated with intravenous contrast administration and is limited in its capacity to characterize and stratify the different vascular layers of the optic nerve and retina. The use of new imaging techniques, such as optical coherence tomographic angiography (Angio-OCT), is therefore important. Aim: A qualitative description is made of the vascular layers of the optic nerve and of how vascular events affect radial peripapillary capillaries (RPC). Two patients with central retinal artery occlusion (CRAO), …

Pathologymedicine.medical_specialtygenetic structuresShort ReportUlls Cirurgia01 natural sciences03 medical and health scienceschemistry.chemical_compound0302 clinical medicinelcsh:OphthalmologyOphthalmologymedicineradial peripapillary capillaries (RPC)posterior ciliary artery0101 mathematicsarteritic anterior ischemic optic neuropathy (AAION)Retinamedicine.diagnostic_testcentral retinal artery occlusion (CRAO)business.industry010102 general mathematicsRetinalFluorescein angiographymedicine.diseaseeye diseasesArteritic anterior ischemic optic neuropathymedicine.anatomical_structurechemistrylcsh:RE1-994Angiography030221 ophthalmology & optometryOptic nerveCentral retinal artery occlusionsense organsbusinessPerfusionAngio-OCTOphthalmology and Eye Diseases
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Subtle retinal pathology in amyotrophic lateral sclerosis

2014

Amyotrophic lateral sclerosis (ALS) is characterized by neuro-ophthalmological abnormalities beyond disturbed oculomotor control such as decreased visual acuity and disturbed visual evoked potentials. Here we report retinal alterations in a cohort of 24 patients with clinically definite (n = 20) or probable (n = 4) ALS as compared to matched controls. High-resolution spectral domain optical coherence tomography with retinal segmentation revealed a subtle reduction in the macular thickness and the retinal nerve fiber layer (RNFL) as well as a marked thinning of the inner nuclear layer (INL). Our data indicate an unprecedented retinal damage pattern and suggest neurodegeneration beyond the mo…

Pathologymedicine.medical_specialtymedicine.diagnostic_testgenetic structuresbusiness.industryGeneral NeuroscienceNeurodegenerationNerve fiber layerRetinalmedicine.diseaseeye diseaseschemistry.chemical_compoundmedicine.anatomical_structurechemistryOptical coherence tomographyMotor systemDecreased Visual AcuityInner nuclear layermedicineNeurology (clinical)sense organsAmyotrophic lateral sclerosisbusinessBrief CommunicationsAnnals of Clinical and Translational Neurology
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Retinopathy of prematurity-current diagnosis and management

1993

Despite advances in ophthalmological care of premature infants, retinopathy of prematurity (ROP) remains a still unsolved problem for paediatricians as well as ophthalmologists. A survey of the current literature concerning drug therapy and surgical management as related to the different stages of ROP is given. The classification system for ROP according to the International Committee is presented as well as our screening policy in relation to the literature. The effectiveness in preventing severe cases of ROP and the toxicity of vitamin E supplementation in high-risk premature infants is still disputed and no recommendations can be given. Cryotherapy is recommended in symmetric cases of st…

Pediatricsmedicine.medical_specialtygenetic structuresmedicine.medical_treatmentEye diseaseVitrectomyCryotherapyCryosurgeryPharmacotherapyVitrectomymedicineHumansMass ScreeningRetinopathy of Prematuritybusiness.industryInfant NewbornRetinal detachmentRetinopathy of prematurityPrognosismedicine.diseaseeye diseasesSurgeryScleral BucklingPediatrics Perinatology and Child Healthsense organsbusinessScleral bucklingInfant PrematureRetinopathyEuropean Journal of Pediatrics
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Pharmacological characterization of high-affinity σ1 receptor ligands with spirocyclic thienopyran and thienofuran scaffold

2019

Abstract Objectives In this study, the pharmacological properties of six spirocyclic piperidines 1–6 showing very high σ1 receptor affinity (Ki = 0.2–16 nm) were investigated. Methods In vitro receptor binding studies, retinal ganglion assay and in vivo capsaicin assay were used to determine the affinity, selectivity and activity. Influence on human tumour cell growth (cell lines A427, LCLC-103H, 5637 and DAN-G) was determined in different assays. The effect on the ergosterol and cholesterol biosynthesis was determined by GLC/MS analysis. Key findings Receptor binding studies demonstrated high selectivity for the σ1 receptor. The increased Ca2+ influx mediated by 2 and the analgesic activit…

Pharmacology0303 health sciencesErgosterol010405 organic chemistryCell growthCellPharmaceutical Science01 natural sciencesRetinal ganglionIn vitroSterol0104 chemical sciences03 medical and health scienceschemistry.chemical_compoundmedicine.anatomical_structurechemistryBiochemistryCell cultureIn vivomedicine030304 developmental biologyJournal of Pharmacy and Pharmacology
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The α1B-adrenoceptor subtype mediates adrenergic vasoconstriction in mouse retinal arterioles with damaged endothelium

2014

Background and Purpose The α1-adrenoceptor family plays a critical role in regulating ocular perfusion by mediating responses to catecholamines. The purpose of the present study was to determine the contribution of individual α1-adrenoceptor subtypes to adrenergic vasoconstriction of retinal arterioles using gene-targeted mice deficient in one of the three adrenoceptor subtypes (α1A-AR−/−, α1B-AR−/− and α1D-AR−/− respectively). Experimental Approach Using real-time PCR, mRNA expression for individual α1-adrenoceptor subtypes was determined in murine retinal arterioles. To assess the functional relevance of the three α1-adrenoceptor subtypes for mediating vascular responses, retinal vascular…

Pharmacologymedicine.medical_specialtyEndotheliumAdrenergic receptorVideo microscopyRetinalBiologymedicine.diseasechemistry.chemical_compoundEndocrinologymedicine.anatomical_structurechemistryInternal medicinemedicinePrazosinmedicine.symptomEndothelial dysfunctionPhenylephrineVasoconstrictionmedicine.drugBritish Journal of Pharmacology
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Dephosphorylation of Centrins by Protein Phosphatase 2C α and β.

2009

In the present study, we identified protein phosphatases dephosphorylating centrins previously phosphorylated by protein kinase CK2. The following phosphatases known to be present in the retina were tested: PP1, PP2A, PP2B, PP2C, PP5, and alkaline phosphatase. PP2C 𝛼 and 𝛽 were capable of dephosphorylating P-Thr138-centrin1 most efficiently. PP2C𝛿 was inactive and the other retinal phosphatases also had much less or no effect. Similar results were observed for centrins 2 and 4. Centrin3 was not a substrate for CK2. The results suggest PP2C 𝛼 and 𝛽 to play a significant role in regulating the phosphorylation status of centrins in vivo.

PhosphatasePyruvate dehydrogenase phosphataseBioinformaticsDephosphorylationlcsh:Chemistrylcsh:QD241-441lcsh:Biochemistrychemistry.chemical_compoundlcsh:Organic chemistryIn vivoResearch LetterMedicinelcsh:QD415-436lcsh:Sciencelcsh:QH301-705.5Earth-Surface Processesbusiness.industryRetinalProtein phosphatase 2Biochemistrychemistrylcsh:Biology (General)lcsh:QD1-999embryonic structuresAlkaline phosphatasePhosphorylationlcsh:QbusinessResearch letters in biochemistry
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