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Salgueiro Barboni, Mirella Telles
;
Gomes Martins, Cristiane Maria
;
Nagy, Balazs Vince
;
Tsai, Tina
;
Damico, Francisco Max
;
da Costa, Marcelo Fernandes
;
Pavanello, Rita de Cassia M.
;
Vilaca Lourenco, Naila Cristina
;
Pereirade Cerqueira, Antonia Maria
;
Zatz, Mayana
;
Kremers, Jan
;
Ventura, Dora Fix
Número total de Autores: 12
|
| Tipo de documento: | Artigo Científico |
| Fonte: | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE; v. 57, n. 8, p. 3581-3587, JUL 2016. |
| Citações Web of Science: | 1 |
| Resumo | |
PURPOSE. Visual information is processed in parallel pathways in the visual system. Parallel processing begins at the synapse between the photoreceptors and their postreceptoral neurons in the human retina. The integrity of this first neural connection is vital for normal visual processing downstream. Of the numerous elements necessary for proper functioning of this synaptic contact, dystrophin proteins in the eye play an important role. Deficiency of muscle dystrophin causes Duchenne muscular dystrophy (DMD), an X-linked disease that affects muscle function and leads to decreased life expectancy. In DMD patients, postreceptoral retinal mechanisms underlying scotopic and photopic vision and ON-and OFF-pathway responses are also altered. METHODS. In this study, we recorded the electroretinogram (ERG) while preferentially activating the (red-green) opponent or the luminance pathway, and compared data from healthy participants (n = 16) with those of DMD patients (n = 10). The stimuli were heterochromatic sinusoidal modulations at a mean luminance of 200 cd/m(2). The recordings allowed us also to analyze ON and OFF cone-driven retinal responses. RESULTS. We found significant differences in 12-Hz response amplitudes and phases between controls and DMD patients, with conditions with large luminance content resulting in larger response amplitudes in DMD patients compared to controls, whereas responses of DMD patients were smaller when pure chromatic modulation was given. CONCLUSIONS. The results suggest that dystrophin is required for the proper function of luminance and red-green cone opponent mechanisms in the human retina. (AU) | |
| Processo FAPESP: | 14/26818-2 - Desenvolvimento e implantação de métodos de avaliação visual: aplicações clínicas e em modelos animais |
| Beneficiário: | Dora Selma Fix Ventura |
| Modalidade de apoio: | Auxílio à Pesquisa - Temático |
| Processo FAPESP: | 12/51299-3 - International joint research on the development and application of electroretinographic and psychophysical methods for the assessment of postreceptoral on-and off-mechanisms in both chromatic and luminance retinal visual pathways in Duchenne muscular dystrophy and in Diabetes mellitus |
| Beneficiário: | Dora Selma Fix Ventura |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 12/01115-3 - Desenvolvimento e aplicação de métodos eletroretinográficos e psicofísicos para avaliação de mecanismos on e off nas vias visuais de luminância e de oponência cromática na Diabetes Mellitus e na distrofia muscular de Duchenne |
| Beneficiário: | Dora Selma Fix Ventura |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 14/06457-5 - Instrumentação científica aplicada aos estudos dos processos visuais desenvolvidos no Laboratório da Visão - IPUSP |
| Beneficiário: | Dora Selma Fix Ventura |
| Modalidade de apoio: | Auxílio à Pesquisa - Pesquisador Visitante - Internacional |
| Processo FAPESP: | 13/08028-1 - CEGH-CEL - Centro de Estudos do Genoma Humano e de Células-Tronco |
| Beneficiário: | Mayana Zatz |
| Modalidade de apoio: | Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs |