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1.
Neurol Res ; 19(5): 551-4, 1997 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-9329035

RESUMEN

In AIDS patients, axonal degeneration in the optic nerve occurs as a histopathological manifestation of the optic neuropathy. Direct infection of neurons by HIV is unlikely, and the axonal injury may be an indirect effect mediated by cytotoxic factors such as tumor necrosis factor-alpha (TNF-alpha) which we have previously demonstrated to cause axonal degeneration in the rabbit optic nerve. To test the suppressive effects of pentoxifylline in preventing TNF-alpha-mediated axonal degeneration, we applied pentoxifylline to an established rabbit model that demonstrates an AIDS-like optic neuropathy using intravitreal TNF-alpha injections. Degenerated axonal profiles were numerous in control rabbit optic nerve (mean 1879) and reduced in rabbits receiving the medium dose of pentoxifylline (300 mg PO BID, mean 439, p < 0.001) and the highest dose of pentoxifylline (600 mg PO BID, mean 120, p < 0.007). High dose pentoxifylline reduced TNF-alpha-induced axonal losses to less than 10% that seen without pentoxifylline pretreatment. Lower doses of pentoxifylline had a lesser but significant protective effect. Our results suggest that TNF-alpha-mediated axonal degeneration can be suppressed by high doses of pentoxifylline. Pentoxifylline may therefore be useful in AIDS patients demonstrating neurological or neuro-ophthalmological symptoms.


Asunto(s)
Axones/efectos de los fármacos , Degeneración Nerviosa/prevención & control , Nervio Óptico/efectos de los fármacos , Nervio Óptico/fisiología , Pentoxifilina/farmacología , Factor de Necrosis Tumoral alfa/farmacología , Animales , Axones/fisiología , Axones/ultraestructura , Relación Dosis-Respuesta a Droga , Inyecciones , Nervio Óptico/ultraestructura , Conejos , Cuerpo Vítreo
3.
Br J Ophthalmol ; 79(2): 182-5, 1995 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-7696243

RESUMEN

Both optic nerves were obtained at autopsy from a 28-year-old man with a 2 year history of idiopathic intracranial hypertension who had undergone bilateral optic nerve sheath decompression 14 days before death. Histopathological and ultrastructural examination of the tissue revealed fibroblasts localised to the sites of fenestration. Adipose tissue was also adherent to the optic nerve pia in areas of incised dura. No patent fistula site was observed. It was concluded that filtration of cerebrospinal fluid after optic nerve sheath decompression may occur through an enclosed bleb of fibrosis rather than through an open fistula.


Asunto(s)
Nervio Óptico/ultraestructura , Seudotumor Cerebral/patología , Adulto , Resultado Fatal , Fibroblastos/ultraestructura , Fibrosis , Humanos , Masculino , Microscopía Electrónica , Nervio Óptico/cirugía
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