[A murine model of transitory optic neuropathy based on small interference RNA-induced OPA1 silencing in vivo (gene mutation associated with Kjer's disease)]. / Modèle murin de neuropathie optique transitoire par inhibition in vivo de l'expression d'OPA1 (gène impliqué dans la maladie de Kjer).
J Fr Ophtalmol
; 29(8): 875-80, 2006 Oct.
Article
em Fr
| MEDLINE
| ID: mdl-17075502
ABSTRACT
PURPOSE:
Developing a murine model of OPA1 linked optic neuropathy.METHODS:
Intravitreal injections (in adult C57BL/6J mice) of small interference RNA (siRNA) specific to OPA1 were performed in the left eye. The right eye served as control, injected with nonspecific siRNA (siRNA scramble). Visual evoked potentials and flash electroretinograms were performed 5 and 12 days after injection. Three months after injection, microscopy of optic nerve sections was performed.RESULTS:
The electrophysiological tests showed a significant reduction in the VEP when the siRNA OPA1-injected eye was stimulated, compared with the control eye injected with siRNA scramble. The electroretinogram was normal in both eyes no significant difference between the right and the left eye was found. Three months after injection, no measurable axonal degeneration was found in either eye.CONCLUSION:
The reduced expression of OPA1 based on RNA silencing in adult mice could induce reversible dysfunction of retinal ganglion cells.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Doenças do Nervo Óptico
/
Atrofia Óptica Autossômica Dominante
/
RNA Interferente Pequeno
/
Modelos Animais de Doenças
/
GTP Fosfo-Hidrolases
/
Mutação
Tipo de estudo:
Risk_factors_studies
Limite:
Animals
Idioma:
Fr
Revista:
J Fr Ophtalmol
Ano de publicação:
2006
Tipo de documento:
Article