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1.
Journal of Forensic Medicine ; (6): 256-268, 2012.
Article Dans Chinois | WPRIM | ID: wpr-983744

Résumé

OBJECTIVE@#To explore the applicability of magnetic resonance diffusion tensor imaging (DTI) for diagnosis of pyramidal tract damage in rats.@*METHODS@#Marmarou's model was set up, followed by DTI scanning at 3, 12, 24 and 72 h post trauma to acquire the dispersion parameter of bilateral pyramidal tracts. Moreover, axonal varicosities per square millimeter and the percentage of positive area of axons demonstrated by beta-amyloid precursor protein (beta-APP) immunostaining were obtained, as well as the mean density and sum density of neurofilament (NF) 68 immunostaining.@*RESULTS@#Axial diffusivity (AD), fraction anisotropy (FA) and relative anisotropy (RA) in the pyramidal tract were significantly and continuously reduced and reached to the bottom at 72h post trauma (P < 0.05) in accord with the gradient of axonal damage verified by beta-APP and NF68 immunostaining. Furthermore, the changes of AD, FA and RA showed a significant negative correlation with the beta-APP immunohistochemical results.@*CONCLUSION@#DTI has important value for early diagnosis in pyramidal tract damage.


Sujets)
Animaux , Mâle , Rats , Précurseur de la protéine bêta-amyloïde/métabolisme , Anisotropie , Axones/anatomopathologie , Encéphale/anatomopathologie , Lésions encéphaliques/anatomopathologie , Imagerie par résonance magnétique de diffusion/méthodes , Modèles animaux de maladie humaine , Traitement d'image par ordinateur , Protéines neurofilamenteuses/métabolisme , Tractus pyramidaux/anatomopathologie , Rat Sprague-Dawley , Indice de gravité de la maladie , Facteurs temps
2.
Experimental & Molecular Medicine ; : 236-242, 2009.
Article Dans Anglais | WPRIM | ID: wpr-49344

Résumé

The retinal activity for vision requires a precise synaptic connectivity. Shank proteins at postsynaptic sites of excitatory synapses play roles in signal transmission into the postsynaptic neuron. However, the correlation of Shank 2 expression with neuronal differentiation in the developing retina remains to be elucidated regardless of previous evidences of Shank 2 expression in retina. Herein, we demonstrated that with progression of development, Shank 2 is initially detected in the inner plexiform layer at P2, and then intensively detected in inner plexiform layer, outer plexiform layer, and ganglion cell layer at P14, which was closely colocalized to the neurofilament expression. Shank 2 was, however, not colocalized with glial fibrillary acidic protein. Shank 2 expression was increased in the differentiated retinoblastoma cells, which was mediated by ERK 1/2 activation. Moreover, Shank 2 expression was colocalized with neurofilament at the dendritic region of cells. In conclusion, our data suggests that Shank 2 is expressed in the neurons of the developing retina and could play a critical role in the neuronal differentiation of the developing retina.


Sujets)
Animaux , Souris , Protéines adaptatrices de la transduction du signal/génétique , Astrocytes/cytologie , Différenciation cellulaire/physiologie , Activation enzymatique , Extracellular Signal-Regulated MAP Kinases/métabolisme , Régulation de l'expression des gènes au cours du développement , Souris de lignée C57BL , Protéines de tissu nerveux/génétique , Protéines neurofilamenteuses/métabolisme , Neurones/cytologie , Rétine/cytologie , Rétinoblastome/métabolisme
4.
Biocell ; 20(1): 55-59, Apr. 1996.
Article Dans Anglais | LILACS | ID: lil-336005

Résumé

Ultrastructural synaptic changes of retinal origin in the pars dorsalis lateral geniculate nuclei (dLGN) after enucleation have been studied in this laboratory, showing a filamentous hypertrophy with maximal expression at 4-6 days post-lesion in monkeys (Pecci Saavedra et al., 1970, 1971). The aim of this work was to elucidate the nature of the newly formed filament in dLGN in post-enucleated rats. Male Wistar rats were fixed with 4 paraformaldehyde plus 0.25 glutaraldehyde in 0.1M phosphate buffer, through the abdominal aorta after 3, 5, and 7 days postenucleation. Sections obtained were incubated with antibodies to the phosphorylated portion of the 160 Kd neurofilaments (1:3000) and anti-GFAP (1:25000). There was an increase in 160 Kd neurofilament staining in axons and degenerating nerve endings in dLGN, as well as a typical astroglial immunostained reaction. Our results show that the newly formed neurofilaments after deafferentation are of the 160 Kd type, commonly present in normal axons.


Sujets)
Animaux , Mâle , Rats , Énucléation oculaire , Corps géniculés , Protéines neurofilamenteuses/métabolisme , Synapses , Astrocytes , Dégénérescence nerveuse/physiopathologie , Corps géniculés , Neurones/composition chimique , Neurones/métabolisme , Neurones/ultrastructure , Protéine gliofibrillaire acide/analyse , Protéines neurofilamenteuses/analyse , Rat Wistar , Synapses
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