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1.
Exp Eye Res ; 99: 1-16, 2012 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-22695224

RESUMEN

Different growth factors have been shown to influence the development of form-deprivation myopia and lens-induced ametropias. However, growth factors have relatively little effect on the growth of eyes with unrestricted vision. We investigate whether the combination of insulin-like growth factor 1 (IGF1) and fibroblast growth factor 2 (FGF2) influence ocular growth in eyes with unrestricted vision. Different doses of IGF1 and FGF2 were injected into the vitreous chamber of postnatal chicks. Measurements of ocular dimensions and intraocular pressure (IOP) were made during and at the completion of different treatment paradigms. Histological and immunocytochemical analyses were performed to assess cell death, cellular proliferation and integrity of ocular tissues. Treated eyes had significant increases in equatorial diameter and vitreous chamber depth. With significant variability between individuals, IGF1/FGF2-treatment caused hypertrophy of lens and ciliary epithelia, lens thickness was increased, and anterior chamber depth was decreased. Treated eyes developed myopia, in excess of 15 diopters of refractive error. Shortly after treatment, eyes had increased intraocular pressure (IOP), which was increased in a dose-dependent manner. Seven days after treatment with IGF1 and FGF2 changes to anterior chamber depth, lens thickness and elevated IOP were reduced, whereas increases in the vitreous chamber were persistent. Some damage to ganglion cells was detected in peripheral regions of the retina at 7 days after treatment. We conclude that the extreme myopia in IGF1/FGF2-treated eyes results from increased vitreous chamber depth, decreased anterior chamber depth, and changes in the lens. We propose that factor-induced ocular enlargement and myopia result from changes to the sclera, lens and anterior chamber depth.


Asunto(s)
Modelos Animales de Enfermedad , Ojo/efectos de los fármacos , Factor 2 de Crecimiento de Fibroblastos/toxicidad , Factor I del Crecimiento Similar a la Insulina/toxicidad , Miopía Degenerativa/inducido químicamente , Animales , Animales Recién Nacidos , Cámara Anterior/efectos de los fármacos , Cámara Anterior/patología , Apoptosis/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Pollos , Cuerpo Ciliar/efectos de los fármacos , Cuerpo Ciliar/patología , Relación Dosis-Respuesta a Droga , Combinación de Medicamentos , Ojo/crecimiento & desarrollo , Hipertrofia , Etiquetado Corte-Fin in Situ , Presión Intraocular/efectos de los fármacos , Inyecciones Intravítreas , Cristalino/efectos de los fármacos , Cristalino/patología , Miopía Degenerativa/patología , Tamaño de los Órganos/efectos de los fármacos , ARN Mensajero/metabolismo , Receptor IGF Tipo 1/genética , Receptor de Insulina/genética , Receptores de Factores de Crecimiento de Fibroblastos/genética , Retina/efectos de los fármacos , Retina/patología , Retinoscopía , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
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