RESUMO
The tub gene is a member of a small, well conserved neuronal gene family of unknown function. Mutations within this gene lead to early-onset blindness and deafness, as well as late-onset obesity and insulin resistance. To test the hypothesis that mutations within other members of this gene family would lead to similar phenotypes as observed in tubby mice, and hence have similar functional properties, we have generated null mutants of the tubby-like protein ( Tulp ) 1 gene by homologous recombination. Similarly to tubby mice, Tulp1 (-/-)mice exhibit an early-onset retinal degeneration with a progressive, rapid loss of photoreceptors, further supporting the notion that previously identified mutations within the human TULP1 gene are indeed causative of retinitis pigmentosa. However, in contrast to tubby mice, Tulp1 (-/-)mice exhibited normal hearing ability and, surprisingly, normal body weight despite the fact that both TUB and TULP1 are expressed in the same neurons within the hypothalamus in areas known to be involved in feeding behavior and energy homeo stasis. However, TUB and TULP1 show a distinctly different staining pattern in the nucleus of these neurons, perhaps explaining the difference in body weight between the Tulp1 (-/-)and tubby mutant mice.
Assuntos
Proteínas do Olho/genética , Mutação/genética , Obesidade/genética , Degeneração Retiniana/genética , Animais , Química Encefálica/genética , Proteínas do Olho/biossíntese , Fundo de Olho , Células Ciliadas Auditivas Internas/patologia , Testes Auditivos , Humanos , Hipotálamo/metabolismo , Marcação In Situ das Extremidades Cortadas , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Oftalmoscopia , Retina/patologia , Retina/ultraestrutura , Degeneração Retiniana/patologia , Aumento de Peso/genéticaRESUMO
PURPOSE: To characterize ocular abnormalities associated with iris atrophy in DBA/2J mice and to determine whether mice of this strain develop elevated intraocular pressure (IOP) and glaucoma. METHODS: Different approaches, including slit-lamp biomicroscopy, ophthalmoscopic examination, ultrasound backscatter microscopy, and histology were used to examine the eyes of DBA/2J mice ranging from 2 to 30 months old. IOP was measured in DBA/2J mice of different ages. RESULTS: DBA/2J mice were found to develop pigment dispersion, iris transillumination, iris atrophy, anterior synechias, and elevated IOP. IOP was elevated in most mice by the age of 9 months. These changes were followed by the death of retinal ganglion cells, optic nerve atrophy, and optic nerve cupping. The prevalence and severity of these lesions increased with age. Optic nerve atrophy and optic nerve cupping was present in the majority of mice by the age of 22 months. CONCLUSIONS: DBA/2J mice develop a progressive form of secondary angle-closure glaucoma that appears to be initiated by iris atrophy and the associated formation of synechias. This mouse strain represents a useful model to evaluate mechanisms of pressure-related ganglion cell death and optic nerve atrophy, and to evaluate strategies for neuroprotection.
Assuntos
Síndrome de Exfoliação/patologia , Oftalmopatias Hereditárias/patologia , Glaucoma de Ângulo Fechado/patologia , Iris/patologia , Envelhecimento/patologia , Animais , Segmento Anterior do Olho/patologia , Atrofia , Morte Celular , Modelos Animais de Doenças , Progressão da Doença , Síndrome de Exfoliação/etiologia , Síndrome de Exfoliação/genética , Oftalmopatias Hereditárias/etiologia , Oftalmopatias Hereditárias/genética , Feminino , Glaucoma de Ângulo Fechado/etiologia , Glaucoma de Ângulo Fechado/genética , Pressão Intraocular , Masculino , Camundongos , Camundongos Endogâmicos DBA , Hipertensão Ocular/etiologia , Hipertensão Ocular/genética , Hipertensão Ocular/patologia , Atrofia Óptica/etiologia , Atrofia Óptica/patologia , Células Ganglionares da Retina/patologiaRESUMO
To evaluate the effects of long-term total parenteral nutrition (TPN) on eye function, 27 adults and 12 children in the UCLA Home TPN Clinic underwent ophthalmoscopic examination and visual-function testing. Direct inspection of the fundus showed a marked granularity of the retinal pigmented epithelium in some patients. About one-half of the children and one-third of the adults tested had at least one and usually two abnormalities in their electroretinogram. Determination of blood nutrients thought to affect vision revealed that zinc and vitamin E were within normal range. Vitamin A concentrations were above normal in 10 of 19 adults and selenium concentrations were below normal in 10 of 10 children and 17 of 21 adults tested. Linoleic and linolenic acid concentrations were low; plasma, platelet, and urine taurine concentrations were significantly lower than normal. Despite these diffuse nutrient abnormalities, only zinc and vitamin E concentrations correlated significantly with any index of visual function.
Assuntos
Nutrição Parenteral Total/efeitos adversos , Transtornos da Visão/etiologia , Adolescente , Adulto , Idoso , Criança , Pré-Escolar , Eletrorretinografia , Feminino , Humanos , Lactente , Ácidos Linolênicos/sangue , Masculino , Pessoa de Meia-Idade , Retina/fisiopatologia , Selênio/sangue , Taurina/sangue , Transtornos da Visão/patologia , Transtornos da Visão/fisiopatologia , Vitamina A/sangue , Vitamina E/sangue , Zinco/sangueRESUMO
Twenty-one children and 23 adults receiving long-term total parenteral nutrition (TPN) for 27 +/- 23 (SD) months were investigated to determine if they were taurine-deficient because the TPN solutions were taurine-free. The fasting plasma taurine level was reduced in the children to 26 + 13 mumol/liter vs the control 57 +/- 16 mumol/liter (P greater than 0.001). The plasma taurine level was significantly reduced in those adults who absorbed less than 25% of their nutritional needs from their diet. Electroretinograms were abnormal in each of eight children who were examined; isolated cone and rod implicit times were both significantly delayed. Electroretinograms were not abnormal in those adults with low plasma taurine levels. Taurine was added to the TPN solutions of four children, and the plasma taurine level became normal in each of them. Electroretinograms of three of these children became normal. One year after discontinuing intervenous taurine supplementation, the plasma taurine level became abnormal in two of three children. These observations indicate that children, and possibly adults, receiving long-term TPN have a nutritional requirement for taurine.