RESUMO
We report on the long-term safety of AAV2.sFlt-1 (a recombinant adeno-associated virus serotype 2 carrying the soluble form of the Flt-1 receptor) injection into the subretinal space of non-human primates. Levels of sFlt-1 protein were significantly higher (P<0.05) in the vitreous of four out of five AAV2.sFlt-1-injected eyes. There was no evidence of damage to the eyes of animals that received subretinal injections of AAV2.sFlt-1; ocular examination showed no anterior chamber flare, normal fundus and electroretinography responses equivalent to those observed before treatment. Notably, immunological analysis demonstrated that gene therapy involving subretinal injection of AAV2.sFlt-1 does not elicit cell-mediated immunity. Biodistribution analysis showed that AAV2.sFlt-1 could be detected only in the eye and not in the other organs tested. These data indicate that gene therapy with subretinal AAV2.sFlt-1 is safe and well tolerated, and therefore promising for the long-term treatment of neovascular diseases of the eye.
Assuntos
Dependovirus/genética , Terapia Genética , Neovascularização Retiniana/terapia , Receptor 1 de Fatores de Crescimento do Endotélio Vascular/genética , Animais , Terapia Genética/efeitos adversos , Vetores Genéticos , Macaca fascicularis , Retina/imunologia , Retina/metabolismo , Neovascularização Retiniana/genética , Neovascularização Retiniana/imunologia , Receptor 1 de Fatores de Crescimento do Endotélio Vascular/imunologia , Receptor 1 de Fatores de Crescimento do Endotélio Vascular/metabolismoRESUMO
The soluble protein composition of Macaque monkey vitreous humour was studied in order to understand its iron-binding properties. The protein content of vitreous humour was 217 micrograms/ml +/- 4.6%, 40% of which was serum albumin and 30% an iron-binding protein of hydrodynamic properties identical to that of transferrin or lactoferrin. Relative to serum, the vitreous humour contained a 13-fold excess of this protein(s). Isoelectric focusing, iron-binding and immunoelectrophoretic studies indicated that both vitreous humour and aqueous humour contained lactoferrin as well as serum transferrin. The iron-binding capacity of these proteins in vitreous humour was equivalent to the mass of haemoglobin iron contained in at least 570000 monkey erythrocytes. It was concluded that the intraocular lactoferrin originated from within the eye. These iron-binding proteins may play a protective role in ocular disturbances such as vitreous haemorrhage, iron foreign body toxicity and infection.
Assuntos
Proteínas de Transporte/análise , Ferro/análise , Corpo Vítreo/análise , Animais , Eletroforese em Gel de Poliacrilamida , Imunoeletroforese , Proteínas de Ligação ao Ferro , Macaca fascicularis , Peso Molecular , Proteínas de Ligação a TransferrinaRESUMO
Factors in vitreous humour which regulate prostaglandin production were investigated using cultured rabbit chorioretinal fibroblasts. These cells produced predominantly prostaglandin E2, 6-ketoprostaglandin F1 alpha, a compound likely to be a metabolite of prostaglandin E2 and 5-hydroxyeicosatetraenoic acid. The synthesis of 6-ketoprostaglandin F1 alpha was nearly completely inhibited by the cyclooxygenase inhibitor aspirin and partially inhibited by 10(-6) M dexamethasone (49%) and 10(-5) M forskolin (68%). Addition of 10% rabbit vitreous humour to subconfluent cells maintained in Dulbecco's modified Eagle's medium plus 1% fetal bovine serum resulted in stimulation of 6-ketoprostaglandin F1 alpha production by as much as 246% as measured by radioimmunoassay. Chorioretinal fibroblasts labelled by [3H]arachidonic acid incorporation into cellular phospholipids synthesised greater amounts of all labelled arachidonic acid metabolites in response to vitreous humour. It was concluded, therefore, that there are factors present in vitreous humour of molecular weight above 10 kDa which are capable of stimulating cellular cyclooxygenase activity. Confluent cells also responded to a factor(s) present in vitreous humour. The fraction of less than 10 kDa inhibited 6-ketoprostaglandin F1 alpha production by 50% when used at a concentration of 10%. Furthermore, 6-ketoprostaglandin F1 alpha production in confluent cells (but not subconfluent cells) was inhibited to 40% of control levels by vitamin C at a concentration of 1 mg/100 ml. The latter result points to an inhibitory role for vitamin C in vitreous humour. We conclude, therefore, that vitreous humour contains factors important for the regulation of prostaglandin metabolism in the eye.
Assuntos
Corioide/citologia , Fibroblastos/metabolismo , Prostaglandinas/biossíntese , Retina/citologia , Corpo Vítreo/análise , Animais , Ácido Araquidônico , Ácidos Araquidônicos/metabolismo , Ácido Ascórbico/farmacologia , Aspirina/farmacologia , Células Cultivadas , Colforsina/farmacologia , Dexametasona/farmacologia , Ativação Enzimática/efeitos dos fármacos , Masoprocol/farmacologia , Prostaglandina-Endoperóxido Sintases/metabolismo , CoelhosRESUMO
The prevalence of diabetic complications is reported from a cross-sectional study of rural diabetic subjects in Western Australia. Logistic-regression analysis has been used to discover potential risk factors associated with each complication. A distinction has been made between time-related variables (age, age at diagnosis, duration of diabetes) and other risk variables. We have attempted to identify the major time-related risk variables for each complication and then examined the effect of other risk variables after accounting for the major time-related variables. The important time-related variables were found to be duration of diabetes for retinopathy, age for macrovascular disease, duration and age at diagnosis of diabetes for sensory neuropathy, and age for renal impairment. When matched on these important time-related variables, the overall prevalences of complications for insulin-dependent (IDDM) compared with non-insulin-dependent (NIDDM) diabetic patients were essentially the same. An exception is renal impairment, for which IDDM patients had a higher prevalence than did NIDDM patients of the same age. After allowing for time-related variables, the analysis also demonstrates positive independent associations between diabetic control (glycosylated hemoglobin) and retinopathy and between diabetic control and macrovascular disease. Plasma cholesterol (positively) and high-density lipoprotein cholesterol (negatively) were related independently to both macrovascular disease and renal impairment. Very few differences in the risk-factor profiles for complications were found for IDDM compared with NIDDM patients after allowing for time-related variables.
Assuntos
Complicações do Diabetes , Fatores Etários , Austrália , Diabetes Mellitus Tipo 1/complicações , Diabetes Mellitus Tipo 2/complicações , Angiopatias Diabéticas/epidemiologia , Nefropatias Diabéticas/epidemiologia , Neuropatias Diabéticas/epidemiologia , Retinopatia Diabética/epidemiologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Risco , Fatores Sexuais , Fatores de TempoRESUMO
Keratoprosthesis research has been a gradual, rather fragmentary process with advances being made by isolated groups of researchers. This has arisen partly because of poor funding in the area; research groups which have achieved commercial support have often had constraints upon the full disclosure of their findings. Despite these difficulties there has been real progress over the last decade by several independent groups. This article concentrates upon our own development of a hydrogel core-and-skirt keratoprosthesis, the Chirila KPro, in order to illustrate the scientific and clinical problems common to keratoprosthesis research. Pilot data from a clinical trial is presented and the priorities for future research are discussed.
Assuntos
Córnea/fisiologia , Próteses e Implantes , Animais , Previsões , Humanos , Hidrogéis , Projetos Piloto , Resultado do TratamentoRESUMO
AIM: To generate a mouse model for slow progressive retinal neovascularisation through vascular endothelial growth factor (VEGF) upregulation. METHODS: Transgenic mice were generated via microinjection of a DNA construct containing the human VEGF165 (hVEGF) gene driven by a truncated mouse rhodopsin promoter. Mouse eyes were characterised clinically and histologically and ocular hVEGF levels assayed by ELISA. RESULTS: One transgenic line expressing low hVEGF levels showed mild clinical changes such as focal fluorescein leakage, microaneurysms, venous tortuosity, capillary non-perfusion and minor neovascularisation, which remained stable up to 3 months postnatal. Histologically, there were some disturbance and thinning of inner and outer nuclear layers, with occasional focal areas of neovascularisation. By contrast, three other lines expressing high hVEGF levels presented with concomitantly severe phenotypes. In addition to the above, clinical features included extensive neovascularisation, haemorrhage, and retinal detachment; histologically, focal to extensive areas of neovascularisation associated with retinal folds, cell loss in the inner and outer nuclear layers, and partial retinal detachment were common. CONCLUSIONS: The authors generated four hVEGF overexpressing transgenic mouse lines with phenotypes ranging from mild to severe neovascularisation. These models are a valuable research tool to study excess VEGF related molecular and cellular changes and provide additional opportunities to test anti-angiogenic therapies.
Assuntos
Camundongos Transgênicos/genética , Neovascularização Retiniana/genética , Fator A de Crescimento do Endotélio Vascular/genética , Animais , Retinopatia Diabética/genética , Retinopatia Diabética/patologia , Modelos Animais de Doenças , Angiofluoresceinografia/métodos , Humanos , Camundongos , Camundongos Endogâmicos C57BL , Fenótipo , Descolamento Retiniano/genética , Descolamento Retiniano/patologia , Hemorragia Retiniana/genética , Hemorragia Retiniana/patologia , Neovascularização Retiniana/patologia , Vasos Retinianos/patologia , Vasos Retinianos/fisiologia , Regulação para Cima/genéticaRESUMO
Pathological angiogenesis, or the production of new capillary vessels from preexisting vasculature, within the eye is a serious event that often leads to blindness. Upregulation of vascular endothelial growth factor (VEGF) has been linked to neovascularization in the eye, suggesting that it could be a suitable target to inhibit angiogenic changes. This work investigated whether the presence of a proven antiangiogenic factor, the soluble variant of the VEGF receptor, sFlt-1, in the anterior chamber is sufficient to inhibit new vessel formation in the cornea in an animal model of corneal neovascularization. A recombinant adenovirus vector that can mediate efficient in vivo gene transfer and expression in ocular cells was selected as a delivery agent. We have shown that after the injection of Ad.betagal into the anterior chamber of normal and cauterized rat eyes, corneal endothelial cells and cells of the trabecular meshwork were efficiently transduced and that beta-galactosidase (beta-Gal) expression was maintained up to 10 days postinjection. Cauterization significantly increased the amount of immunoreactive VEGF in vehicle- or Ad.null-injected animals (t test, p < 0.001 and p < 0.001, respectively). However, when cauterization was combined with Ad.sflt injection there was no statistically significant increase in the amount of immunoreactive VEGF (p = 0.12). The injection of Ad.sflt into the anterior chamber slowed or inhibited VEGF-induced angiogenic changes. After cauterization, 100% of uninjected and vehicle-injected and 82% of Ad.null-injected animals developed moderate to severe corneal angiogenesis in contrast to 18% of Ad.sflt-injected animals. These in vivo results suggest that the transient presence of antiangiogenic agents in the anterior chamber can be successfully used to inhibit the development of corneal angiogenesis.
Assuntos
Inibidores da Angiogênese/farmacologia , Córnea/irrigação sanguínea , Neovascularização da Córnea/terapia , Fatores de Crescimento Endotelial/genética , Linfocinas/genética , Neovascularização Patológica , Proteínas Proto-Oncogênicas/biossíntese , Proteínas Proto-Oncogênicas/genética , Receptores Proteína Tirosina Quinases/biossíntese , Receptores Proteína Tirosina Quinases/genética , Adenoviridae/genética , Animais , Western Blotting , Linhagem Celular , Córnea/metabolismo , Endotélio Vascular/citologia , Olho/metabolismo , Vetores Genéticos , Humanos , Processamento de Imagem Assistida por Computador , Imuno-Histoquímica , Nitratos/farmacologia , Compostos de Potássio/farmacologia , Ratos , Nitrato de Prata/farmacologia , Fatores de Tempo , Transdução Genética , Transgenes , Veias Umbilicais/citologia , Regulação para Cima , Fator A de Crescimento do Endotélio Vascular , Receptor 1 de Fatores de Crescimento do Endotélio Vascular , Fatores de Crescimento do Endotélio Vascular , beta-Galactosidase/metabolismoRESUMO
The purpose of this study was to evaluate recombinant adeno-associated virus (AAV) as an in vivo gene transfer vector for the retina and to explore the possibility of monitoring the expression of green fluorescent protein (GFP) using a noninvasive method. Rats were injected subretinally with rAAV-gfp or rAAV-lacZ. Strong expression of the reporter gene in a circular area surrounding the injection site was observed in retinal whole mounts and tissue sections. Higher magnification revealed that cells demonstrating high levels of green fluorescence were hexagonal in shape, indicating they were retinal pigment epithelium (RPE) cells. Histological observation of retinal sections demonstrated that recombinant AAV specifically transduced RPE cells. Ten animals were injected with rAAV-gfp for longitudinal studies and the fluorescence was monitored by retinal fluorescence photography. The GFP signal was detected in 100% of the animals as early as 2 weeks postinjection and remained present throughout the experimental period of 4 months. After 2 weeks, a gradual increase in the number of transduced cells occurred before reaching maximal levels of GFP expression at 8 weeks. This was followed by a small decrease over 4 weeks before reaching stable expression at 16 weeks. Our results demonstrated that rAAV efficiently transduces rat RPE cells and that retinal fluorescence photography is suitable for monitoring GFP expression. By using this noninvasive technique, we demonstrated that repetitive measurements of GFP expression in vivo in the rAAV-gfp-transduced retina are possible. This study demonstrated that retinal fluorescence photography is a potent tool for studying AAV-mediated gene delivery in the retina.
Assuntos
Dependovirus/genética , Técnicas de Transferência de Genes/normas , Vetores Genéticos , Retina/metabolismo , Animais , Resistência a Medicamentos/genética , Estudos de Avaliação como Assunto , Fluorescência , Proteínas de Fluorescência Verde , Proteínas Luminescentes/genética , Neomicina/farmacologia , Fotografação , Ratos , Recombinação Genética , Transdução GenéticaRESUMO
A wide variety of retinal pathology is associated with an increase in Müller glial cell expression of glial fibrillary acidic protein (GFAP). In this study the time course and spatial spread of the Müller cell GFAP response following argon laser photocoagulation lesions was examined in wholemounted rabbit retina. At 24 hours single focal lesions were surrounded by GFAP positive Müller cell end feet which declined in density with distance but extended as far as 2-3 mm from the lesion. The Müller cell reaction reached a maximal spread of 4-5 mm at 14 to 21 days and had started to contract by 30 days, leaving a core of GFAP positive processes immediately around the lesion site at 60 days. This zone of spread was much larger than the area of disrupted pigment epithelium. Isodensity plots did not reveal any correlation with the trajectory of retinal ganglion cell axons. The spread of reaction was more confined for lesions within the visual streak than in the dorsal or ventral retinal periphery. Multiple lesions within a focal region of retina resulted in a greater density of GFAP reactive end feet with a corresponding greater spread. However, when five to ten lesions were made in a horizontal row, the Müller cells over the entire retina became GFAP immunoreactive. This pan-retinal reaction took several days to spread, peaked at 7-14 days, and contracted back to the primary lesion sites by 2 months. This spread of Müller cell reactivity may be triggered by the diffusion of substances released by injury or it may be due to direct cellular communication. The extensive indirect effect on Müller cells of laser irradiation might be an important component of the clinical effect of laser photocoagulation and indicates a long distance communication mechanism between retinal glia which is poorly understood. This study also shows the importance of the time at which the Müller cell response is assessed.
Assuntos
Neuroglia/fisiologia , Coelhos/fisiologia , Retina/fisiologia , Animais , Axônios/ultraestrutura , Proteína Glial Fibrilar Ácida/análise , Neuroglia/química , Epitélio Pigmentado Ocular/citologia , Retina/citologia , Retina/lesõesRESUMO
The effect of systemic hypoxia on the maintained firing rate (MFR) of single retinal ganglion cells has been measured in the cat at a constant luminance level. Systemic hypoxia was produced by reducing the percentage of oxygen in the respiratory mixture under forced ventilation so that arterial PCO2 and pH were constant. Extracellular recordings were obtained from both X and Y retinal ganglion cells before, during, and after systemic hypoxia, with each cell acting as its own control. The MFR was unaltered by arterial PO2 levels of greater than 45 mm Hg. However, at and below this level of hypoxia the MFR was reversibly increased in 67% of the cells tested. Whether or not this increase occurred was independent of cell type or location. For arterial PO2 values of 24 to 34 mm Hg the initial increase in MFR was followed by a decrease for these cells; for PO2 values of less than 24 mm Hg the MFR showed a large initial increase followed by a complete cessation of firing. The remaining 33% of cells displayed only reduced MFR during hypoxia. The results indicate that ganglion cell function may be drastically affected by hypoxia. This may be relevant to the visual loss of a variety of retinal disorders.
Assuntos
Hipóxia/fisiopatologia , Retina/fisiopatologia , Potenciais de Ação , Animais , Gatos , Estimulação Luminosa/instrumentação , Estimulação Luminosa/métodosRESUMO
A simplified practical technique for biopsy of retina and choroid has been developed in dogs. A 270 degree circular scleral flap of 3 mm diameter is raised. The risks of chorioretinal bleeding and vitreous loss are greatly reduced by intravenous mannitol and controlled hyperventilation, with hyperoxygenation and transient, systemic hypotension under general anesthesia. Rreasonable ultrastructural detail was preserved in chorioretinal specimens of 1 mm diameter. Repeat biopsies in the same eye are feasible without significant complications.
Assuntos
Biópsia/métodos , Corioide/ultraestrutura , Retina/ultraestrutura , Animais , Cães , Angiofluoresceinografia , Fundo de Olho , Hiperventilação , Hipotensão Controlada , Pressão Intraocular/efeitos dos fármacos , Manitol/administração & dosagem , Oxigênio/administração & dosagemRESUMO
PURPOSE: To investigate the effects of recombinant adenovirus-mediated downregulation of cathepsin S (CatS) on the retinal pigment epithelium and/or neural retina in vivo. METHODS: The expression of green fluorescent protein (gfp) after subretinal injection of a recombinant adenovirus, Ad.gfp, into rat eyes was first established by in vivo fundus fluorescence photography and fluorescence microscopy. The autofluorescent debris accumulation in Ad.CatSAS (recombinant adenovirus carrying the antisense CatS gene)injected rat eyes was monitored by fluorescence microscopy, and the antisense CatS RNA expression was demonstrated by in situ hybridization. Changes in the retinal morphology were assessed by light microscopy. ResuLTS. The gfp expression was present in 30% to 90% of the injection area at 3 days and was absent 9 days after Ad.gfp injection. In Ad.CatSAS-injected eyes, the expression of antisense CatS RNA was demonstrated by in situ hybridization. Autofluorescent debris accumulation was significantly higher in Ad.CatSAS-injected eyes than in control eyes. The shortening of photoreceptor outer segments in Ad.CatSAS-injected eyes coincided with intense autofluorescent debris accumulation. The number of layers of photoreceptor cells decreased with time and were 11, 9, and 8 at 7, 14, and 28 days after Ad.CatSAS injection, respectively. In control eyes, the number of layers of photoreceptor cells (14) remained unchanged. CONCLUSIONS: These results demonstrate that recombinant adenovirus-mediated transient modulation of gene expression in retinal pigment epithelial (RPE) cells could induce changes in the retina, and, in spite of the low expression of endogenous CatS in RPE cells, this enzyme plays an important role in maintenance of normal retinal function.
Assuntos
Adenoviridae/genética , Modelos Animais de Doenças , Técnicas de Transferência de Genes , Células Fotorreceptoras/patologia , Degeneração Retiniana/etiologia , Animais , Catepsinas/genética , Catepsinas/metabolismo , Regulação para Baixo , Fundo de Olho , Expressão Gênica , Proteínas de Fluorescência Verde , Hibridização In Situ , Proteínas Luminescentes/genética , Proteínas Luminescentes/metabolismo , Microscopia de Fluorescência , Células Fotorreceptoras/enzimologia , Células Fotorreceptoras/virologia , Epitélio Pigmentado Ocular/enzimologia , Epitélio Pigmentado Ocular/patologia , Epitélio Pigmentado Ocular/virologia , Ratos , Ratos Mutantes , Degeneração Retiniana/enzimologia , Degeneração Retiniana/patologia , Degeneração Retiniana/virologiaRESUMO
PURPOSE: To examine the nature and dynamics of gene transfer to human retinal pigment epithelium (RPE) using an adenoviral vector and adjuvants that may enhance the uptake of recombinant adenoviruses. METHODS: Human RPE cultures (HRPE7) were transfected in vitro with varying concentrations (4, 20, 40, 120, and 200 pfu/microliter) and for varying periods (1, 2, 4, 16, 24, 48, and 72 hours) with a replication-deficient adenovirus (Ad.RSV. beta gal) containing the bacterial beta-galactosidase transgene (beta gal). The expression of beta gal was monitored by counting after X gal staining. The transgene expression profiles were compared to those of human F2000 fibroblasts under the same conditions. The adjuvant effect of sodium hyaluronate (HA) on the expression of beta gal was tested in F2000 and early and late passage human RPE cells for differing concentrations of HA, viral titers, and incubation times. Immunofluorescent cytochemistry was carried on HRPE7 and F2000 cells for the HA receptors, homing receptor CD44 (CD44), intercellular adhesion molecule 1 (ICAM-1), and the receptor for hyaluronan mediated motility (RHAMM). RESULTS: The number of HRPE7 and F2000 cells expressing the adenoviral transgene increased consistently with increasing incubation time and viral titer. There was a higher uptake of Ad.RSV. beta gal in HRPE7 cells compared to the F2000 fibroblasts under the same conditions. There was an increase of 28.1% and 41.4% in the number of RPE7 cells expressing adenoviral transgene and 16.2% and 15.8% F2000 fibroblast cells expressing the adenoviral transgene in the presence of 0.001% and 0.005% HA, respectively. Significant adjuvant effects on transgene expression also were shown in HRPE51 cells. It appears that the effects of increasing viral titer, length of incubation, and the presence of HA on transgene expression are at least additive. The appearance of CD44 and ICAM receptors on RPE7 and F2000 cells and RHAMM receptors on F2000 cells was similar. The RHAMM receptors in HRPE7 cells, however, were shown preferentially over the nucleus. CONCLUSIONS: On the basis of these results, the authors propose that adenovirus transgene expression increases with increasing incubation time and viral titer in cell culture. The rate of increase of expression differs between human RPE cells and the F2000 fibroblast cells, which may offer a targeting opportunity. The authors propose that the use of HA can offer both an adjuvant effect and a targeting advantage in terms of transferring adenoviral transgenes to human RPE in culture.
Assuntos
Adenovírus Humanos/genética , Epitélio Pigmentado Ocular/enzimologia , Transfecção , beta-Galactosidase/metabolismo , Criança , Vírus Defeituosos , Fibroblastos/citologia , Fibroblastos/efeitos dos fármacos , Fibroblastos/enzimologia , Fibroblastos/virologia , Técnica Indireta de Fluorescência para Anticorpo , Expressão Gênica , Vetores Genéticos , Humanos , Receptores de Hialuronatos/metabolismo , Ácido Hialurônico/farmacologia , Ácido Hialurônico/fisiologia , Molécula 1 de Adesão Intercelular/metabolismo , Pulmão/citologia , Pulmão/efeitos dos fármacos , Pulmão/enzimologia , Pulmão/virologia , Pessoa de Meia-Idade , Epitélio Pigmentado Ocular/citologia , Epitélio Pigmentado Ocular/efeitos dos fármacos , Epitélio Pigmentado Ocular/virologia , beta-Galactosidase/genéticaRESUMO
This study records for the first time the retinal tissue oxygen partial pressure as a function of location within the retina of the domestic cat. Tissue pO2 was recorded with oxygen sensitive microelectrodes that use the polarographic principle. The mean vitreal pO2 close to the internal limiting membrane was 20.2 +/- 2.3 mmHg. The internal limiting membrane does not act as a diffusion barrier for oxygen. As the electrode was advanced into the inner retina, the tissue pO2 rose gradually to a value of 24.6 +/- 2.3 mmHg and then fell to a minimum of 12.0 +/- 5.5 mmHg before rising again to a value of 29.2 +/- 2.5 mmHg. Further insertion resulted in a sudden steep rise of tissue pO2 values to 72.0 +/- 5.1 mmHg, after which there was no further alteration in measured values. Although the exact location within the retina of the recording electrode was not known, it is probable that the tissue pO2 minimum occurs at about the level of the inner nuclear layer. Therefore, it is probable that the retinal avascular layers receive their oxygen supply primarily from the choroidal circulation in the cat.
Assuntos
Gatos/metabolismo , Consumo de Oxigênio , Retina/metabolismo , Animais , Microeletrodos , Oxigênio/sangue , Pressão Parcial , Retina/anatomia & histologia , Corpo Vítreo/metabolismoRESUMO
Continual monitoring of intraocular pressure (IOP) by passive radiotelemetry, with a miniature scleral applanating device, mounted in a haptic contact lens (applanating transensor) is reported in the rabbit and dog. Several prototype transensors were calibrated in vivo in the rabbit and dog; a consistent linear output was obtained for each eye, although reproducibility of the slope between eyes over a period of time was less than ideal. Accuracy of determination of IOP was found to be better for the rabbit and will have to be improved before the instrument can be applied to the human. Multiple regression analysis of calibration studies in six rabbits established that the transensor output was not significantly affected by the small changes in body temperature and atmospheric pressure encountered during the study. Continual scleral tonometry with a standard Mackay-Marg tonometer showed that ocular rigidity has a significant effect on calibration curves, in contradistinction to standard Mackay-Marg corneal tonometry. A time-dependent decay in tonometer readings was more evident in canine eyes with low ocular rigidity. Since the transensor is also a guard-ring applanating device, calibration may be necessary for individual eyes and species.
Assuntos
Pressão Intraocular , Telemetria/instrumentação , Tonometria Ocular/instrumentação , Animais , Pressão Atmosférica , Temperatura Corporal , Calibragem/normas , Cães , Coelhos , Telemetria/métodos , Tonometria Ocular/métodosRESUMO
This paper introduces a new method for supplying oxygen directly to ischemic inner retina, using an oxygen source in the vitreous. Acute retinal vascular occlusion was created in cat eyes by direct pressure on the optic disk and its margins with a glass probe. The satisfactory occlusion of the retinal vessels was documented by direct observation, and functionally by recording the ERG. The vascular occlusion caused a large decrease in the size of the ERG b wave, with no change in the a wave amplitude. The oxygen source was a catheter made of strands of an oxygen-permeable membrane which was inserted into the vitreal cavity. After successful vascular occlusion was documented, 100% gaseous oxygen was perfused through the catheter while recording the ERG. In response to the perfused oxygen the b wave partially recovered. Ventilating the animal with 100% oxygen when the retinal vessels were occluded also caused recovery of the b wave amplitude. Termination of the vitreal oxygen source caused a decrease in b wave amplitude to the level previously observed after the occlusion of the retinal vessels. When the retinal circulation was restored by removal of the glass probe the b wave recovered. The results show that it is possible to supply adequate oxygen to the inner retina via the vitreous to replace the oxygen normally supplied by the retinal circulation. Modification of this method may be useful for the treatment of recent and incomplete retinal vascular occlusion.
Assuntos
Isquemia/tratamento farmacológico , Oxigênio/administração & dosagem , Retina/irrigação sanguínea , Doença Aguda , Animais , Cateterismo/métodos , Gatos , Eletrorretinografia , Fundo de Olho , Isquemia/patologia , Isquemia/fisiopatologia , Oxigênio/uso terapêutico , PermeabilidadeRESUMO
This paper presents the first evidence that in retinas with experimentally induced vascular disease some vessels contain only plasma. This was demonstrated by a histologic technique developed specifically to test the hypothesis that at some stage in retinal vascular disease, vessel patency to erythrocytes is lost before vessels close to plasma. Using this technique, we visualized three major components of the circulation at all retinal locations: the erythrocytes; the plasma as marked by the presence of 0.2-micron fluorescent microspheres; and all functioning endothelial cell nuclei, which were marked by the fluorochrome bis-Benzimide. It was assumed that the distributions of the erythrocytes and small particles in retinal whole mounts reflected accurately the true in vivo distributions at the moment of circulation arrest. Postenucleation the retina can be viewed and photographed within 45 min of circulation arrest. The technique was used on normal rats and on rats induced with a fast-developing model of retinal vasculopathy. With this model, we demonstrated retinal vascular segments perfused by plasma but containing no erythrocytes with functioning endothelial cells in the vessel walls. This may mean that an early factor in some retinal vascular pathologies is tissue hypoxia caused by reduced erythrocyte perfusion.
Assuntos
Eritrócitos/metabolismo , Doenças Retinianas/fisiopatologia , Vasos Retinianos/fisiopatologia , Grau de Desobstrução Vascular , Aloxano , Animais , Retinopatia Diabética/fisiopatologia , Modelos Animais de Doenças , Endotélio Vascular/metabolismo , Corantes Fluorescentes , Masculino , Microesferas , Nitrilas , Plasma/metabolismo , Ratos , Ratos EndogâmicosRESUMO
PURPOSE: To investigate the presence and role of a recently cloned cysteine protease (cathepsin S) in the digestion of rod outer segments (ROS) by cultured retinal pigment epithelial (RPE) cells. METHODS: RPE cell cultures were established from eye bank donor eyes. Total RNA was extracted from freshly harvested cultures, and after reverse transcription, the cDNA was subjected to polymerase chain reaction (PCR). Cathepsin S (Cat S) mRNA translation was inhibited by antisense oligonucleotides, and the effect of inhibition on the accumulation of fluorescent debris was examined. The activity of cysteine and aspartic proteases in ROS-challenged RPE cell cultures was inhibited by leupeptin and pepstatin, respectively. The accumulation of autofluorescent debris within RPE cells was measured by a fluorophotometric flow cytometer. The presence of phagosomes in antisense DNA-inhibited and control cultures was demonstrated by electron microscopy. RESULTS: The expression of Cat S in RPE cells was demonstrated by RNA-PCR. Using antisense oligonucleotide-mediated-specific inhibition of Cat S, a significant ROS-derived increase in autofluorescence was detected within the RPE cells when they were compared with the unchallenged control cultures and cultures in the presence of ROS and sense oligonucleotides. Electron microscopy demonstrated the presence of a large number of phagosomes that enveloped structures similar to ROS. The accumulation of autofluorescent debris was also demonstrated in cysteine protease-inhibited, ROS-challenged RPE cultures, but it was not detected with aspartic protease inhibition. CONCLUSIONS: The expression of Cat S in RPE cells and the accumulation of an autofluorescent debris in cultures in which cysteine proteases or Cat S activity is inhibited suggest a key role for this enzyme, either in the ROS digestion process or in the activation of cathepsin D, the major lysosomal enzyme present in RPE cells.
Assuntos
Catepsinas/análise , Catepsinas/fisiologia , Fagocitose/fisiologia , Epitélio Pigmentado Ocular/enzimologia , Segmento Externo da Célula Bastonete/fisiologia , Animais , Catepsinas/antagonistas & inibidores , Bovinos , Células Cultivadas , DNA Antissenso/farmacologia , Humanos , Oligonucleotídeos/metabolismo , Oligonucleotídeos Antissenso/metabolismo , Fagossomos , Epitélio Pigmentado Ocular/ultraestrutura , Reação em Cadeia da Polimerase , Inibidores de Proteases/farmacologia , Biossíntese de Proteínas/efeitos dos fármacos , RNA Mensageiro/metabolismo , Segmento Externo da Célula Bastonete/citologiaRESUMO
Intravitreal drug administration is the treatment of choice for bacterial endophtalmitis, but improved knowledge of vitreal pharmacokinetics is essential for the development of optimal antibiotic regimes. We used our recently developed sampling device to estimate vitreal gentamicin concentrations for up to 30 hr after an intravitreal bolus injection of gentamicin. The device is based on the principle of dialysis, whereby a constant flow rate of dialysate through a loop of dialysis fiber in the vitreous attains a gentamicin concentration proportional to the intravitreal gentamicin level around the fiber. The dialysate is continuously recovered and the collected samples then assayed for gentamicin. Normal cat eyes and those with induced bacterial endophthalmitis formed the two groups tested. Concentration-time data fitted well to an open single compartment pharmacokinetic model that incorporated the processes of transfer of drug from the injection site to the sampling site (a function of diffusion within the vitreous), and the elimination from the sampling site (a function of elimination from the vitreous). The initial phase of transfer between the injection and sampling site was rapid and rates were comparable in the two groups. Elimination rate constants were uniformly greater in infected eyes than in controls (0.107 hr-1 compared to 0.055 hr-1). Aqueous humor gentamicin concentrations in control eyes varied between 3 and 6 times those found in fellow infected eyes at the end of each experiment. Accelerated elimination of gentamicin from the vitreous body of eyes with endophthalmitis may be explained by increased permeability of the blood-retinal barrier.
Assuntos
Gentamicinas/farmacocinética , Corpo Vítreo/metabolismo , Animais , Humor Aquoso/metabolismo , Gatos , Diálise/instrumentação , Diálise/métodos , Endoftalmite/etiologia , Endoftalmite/metabolismo , Gentamicinas/administração & dosagem , Injeções , Valores de Referência , Infecções Estafilocócicas , Fatores de TempoRESUMO
Proliferative vitreoretinopathy (PVR) results in retinal detachment and visual impairment due to fibroblastic proliferation in the vitreous and subsequent cellular contraction. The authors have used an in vitro model for PVR to evaluate the action of the antineoplastic drug, taxol, on chorioretinal fibroblast proliferation and contractility. Dose response curves obtained show taxol to be a potent inhibitor of both cellular events. Fifty percent inhibition of contraction and proliferation occurred at 2 X 10(-8)M and 3 X 10(-9)M, respectively. On the basis of this pharmacodynamic data, three dosage regimes were chosen to evaluate possible prevention of PVR in an animal model based on the intravitreal injection of cultured fibroblasts. These animals trials show that a single intravitreal dose of either 35 micrograms or 0.5 microgram taxol significantly reduces incidence and extent of PVR. The average grade of vitreoretinal traction at 28 days for 35 micrograms taxol and 250,000 cells was 0.4 (control 1.8); for 35 micrograms taxol and 700,000 cells, 1.0 (control 2.2); and for 0.5 microgram taxol and 250,000 cells, 1.0 (control 2.3). Delayed optic nerve damage was noted with the highest dose used, but a good therapeutic margin may exist. Long-term clinical histopathologic and electrophysiologic studies will be required. The authors conclude from these preliminary studies that taxol holds definite promise for the relief of traction retinal detachment and PVR.