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Neuroscience ; 132(1): 13-32, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15780463

RESUMEN

The present experiment was designed to study changes in behavior following immunolesioning of the basal forebrain cholinergic system. Rats were lesioned at 3 months of age by injection of the 192 IgG-saporin immunotoxin into the medial septum area and the nucleus basalis magnocellularis, and then tested at different times after surgery (from days 7-500) on a range of behavioral tests, administered in the following order: a nonmatching-to-position task in a T-maze, an object-recognition task, an object-location task, and an open-field activity test. The results revealed a two-way interaction between post-lesion behavioral testing time and memory demands. In the nonmatching-to-position task, memory deficits appeared quite rapidly after surgery, i.e. at a post-lesion time as short as 1 month. In the object-recognition test, memory impairments appeared only when rats were tested at late post-lesion times (starting at 15 months), whereas in the object-location task deficits were apparent at early post-lesion times (starting from 2 months). Taking the post-operative time into account, one can hypothesize that at the shortest post-lesion times, behavioral deficits are due to pure cholinergic depletion, while as the post-lesion time increases, one can speculate the occurrence of a non-cholinergic system decompensation process and/or a gradual degeneration process affecting other neuronal systems that may contribute to mnemonic impairments. Interestingly, when middle-aged rats were housed in an enriched environment, 192 IgG-saporin-lesioned rats performed better than standard-lesioned rats on both the nonmatching-to-position and the object-recognition tests. Environment enrichment had significant beneficial effects in 192 IgG-saporin-lesioned rats, suggesting that lesioned rats at late post-lesion times (over 1 year) still have appreciable cognitive plasticity.


Asunto(s)
Núcleo Basal de Meynert/fisiopatología , Corteza Cerebral/fisiopatología , Fibras Colinérgicas/patología , Planificación Ambiental , Trastornos de la Memoria/terapia , Acetilcolina/metabolismo , Animales , Anticuerpos Monoclonales , Núcleo Basal de Meynert/patología , Conducta Animal/fisiología , Corteza Cerebral/patología , Fibras Colinérgicas/metabolismo , Desnervación , Modelos Animales de Enfermedad , Inmunotoxinas , Masculino , Aprendizaje por Laberinto/fisiología , Trastornos de la Memoria/patología , Trastornos de la Memoria/fisiopatología , N-Glicosil Hidrolasas , Plasticidad Neuronal/fisiología , Neurotoxinas , Estimulación Física , Ratas , Ratas Wistar , Reconocimiento en Psicología/fisiología , Proteínas Inactivadoras de Ribosomas Tipo 1 , Saporinas , Núcleos Septales/patología , Núcleos Septales/fisiopatología , Factores de Tiempo
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