Morphological changes in the suprachiasmatic nucleus of aging female marmosets (callithrix jacchus)

The suprachiasmatic nuclei (SCN) are pointed to as the mammals central circadian pacemaker. Aged animals show internal time disruption possibly caused by morphological and neurochemical changes in SCN components. Some studies reported changes of neuronal cells and neuroglia in the SCN of rats and no...

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Detalhes bibliográficos
Autores: Engelberth, Rovena Clara G. J., Silva, Kayo Diogenes de A., Azevedo, Carolina V. de M., Gavioli, Elaine Cristina, Santos, Jose Ronaldo dos, Soares, Joacil Germano, Nascimento Junior, Expedito S., Cavalcante, Judney C., Costa, Miriam Stela M. O., Cavalcante, Jeferson S.
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2014
País:Brasil
Recursos:Universidade Federal do Rio Grande do Norte (UFRN)
Repositorio:Repositório Institucional da UFRN
Idioma:inglés
OAI Identifier:oai:repositorio.ufrn.br:123456789/24706
Acesso em linha:https://repositorio.ufrn.br/jspui/handle/123456789/24706
Access Level:acceso abierto
Palavra-chave:Suprachiasmatic
Pacemaker
NeuN-IR
Descrição
Resumo:The suprachiasmatic nuclei (SCN) are pointed to as the mammals central circadian pacemaker. Aged animals show internal time disruption possibly caused by morphological and neurochemical changes in SCN components. Some studies reported changes of neuronal cells and neuroglia in the SCN of rats and nonhuman primates during aging. The effects of senescence on morphological aspects in SCN are important for understanding some alterations in biological rhythms expression. Therefore, our aim was to perform a comparative study of the morphological aspects of SCN in adult and aged female marmoset. Morphometric analysis of SCN was performed using Nissl staining, NeuN-IR, GFAP-IR, and CB-IR. A significant decrease in the SCN cells staining with Nissl, NeuN, and CB were observed in aged female marmosets compared to adults, while a significant increase in glial cells was found in aged marmosets, thus suggesting compensatory process due to neuronal loss evoked by aging