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J Neurotrauma ; 28(3): 383-400, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-21190396

RESUMO

Magnetic resonance imaging (MRI) suggests that with survival after human traumatic brain injury (TBI), there is ongoing loss of white and grey matter from the injured brain during the chronic phase. However; direct quantitative experimental evidence in support of this observation is lacking. Using the guinea pig stretch-injury optic nerve model, quantitative evidence by stereology of damage to the optic nerve and retina was sought. Stretch injury was applied to the right optic nerve of 15 adult male guinea pigs. Three animals each at 1, 2, 3, 8, or 12 weeks' survival were killed and prepared for transmission electron microscopy (TEM). The estimated number of intact and injured axons within bins of transverse diameters 0-0.5, 0.51-1.0, 1.01-1.5, 1.51-2.0, 2.01-2.5, and 2.51-3.0 µm in the middle segment of each injured optic nerve and from 5 control animals were compared across all survival time points. The estimated numbers of intact and pyknotic retinal ganglion cells from the same animals were also compared. Loss of myelinated fibers continued throughout the experimental period. The most rapid loss was of the largest fibers; loss of intermediate-sized fibers continued, but the numbers of the smallest fibers increased from 3 weeks onward. There was hypertrophy and proliferation of glial cells within the surrounding neuropil. A relatively low-grade loss of retinal ganglion cells occurred throughout the experiment, with about 60% remaining at 12 weeks' survival. We provide quantitative evidence that after traumatic axonal injury (TAI) there is a continuing loss of nerve fibers and their cell bodies from a CNS tract over a 3-month post-traumatic interval.


Assuntos
Axônios/patologia , Axônios/ultraestrutura , Traumatismos do Nervo Óptico/patologia , Nervo Óptico/patologia , Nervo Óptico/ultraestrutura , Análise de Variância , Animais , Cobaias , Imageamento por Ressonância Magnética , Masculino , Microscopia Eletrônica de Transmissão , Bainha de Mielina/patologia , Bainha de Mielina/ultraestrutura , Retina/patologia , Retina/ultraestrutura , Células Ganglionares da Retina/patologia , Células Ganglionares da Retina/ultraestrutura
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