Four-vessel occlusion model using aged male Wistar rats: a reliable model to resolve the discrepancy related to age in cerebral ischemia research
Autor: | Angel Raymundo Martínez-Ponce-de-León, Jesús Alberto Morales-Gómez, Humberto Rodriguez-Rocha, Rodrigo Enrique Elizondo-Omaña, Rodolfo Morales-Avalos, Odila Saucedo-Cárdenas, Rodolfo Amador Salazar-Ybarra, Jesús Ancer-Rodríguez, Alejandro Quiroga-Garza, Aracely Garcia-Garcia, Santos Guzmán-López, Zao Cheng Xu, Oscar Quiroga-García, Eliud Enrique Villarreal-Silva |
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Rok vydání: | 2015 |
Předmět: |
Male
0301 basic medicine Aging medicine.medical_specialty Ischemia Hippocampal formation Neuroprotection Brain Ischemia 03 medical and health sciences 0302 clinical medicine Internal medicine Occlusion Four vessel occlusion medicine Animals Rats Wistar CA1 Region Hippocampal Neurons Mortality rate Brain General Medicine medicine.disease Surgery Cerebrovascular Disorders Disease Models Animal 030104 developmental biology Cardiology Anatomy Psychology 030217 neurology & neurosurgery |
Zdroj: | Anatomical Science International. 91:226-237 |
ISSN: | 1447-073X 1447-6959 |
DOI: | 10.1007/s12565-015-0286-x |
Popis: | Animal models of cerebral ischemia have typically been established and performed using young animals, even though cerebral ischemia (CI) affects primarily elderly patients. This situation represents a discrepancy that complicates the translation of novel therapeutic strategies for CI. Models of transient global CI using aged animals have demonstrated an apparent neuroprotective effect on CA1 hippocampal neurons; however, this effect is not completely understood. Our study used a model in which young (3-6 months) and aged (18-21 months) male Wistar rats were subjected to 15 min of transient global CI using the four-vessel occlusion (4 VO) model. We determined that the 4 VO model can be performed on aged rats with a slight increase in mortality rate. In aged rats, the morphological damage was completely established by the 4th day after reperfusion, displaying no difference from their younger counterparts. These results demonstrated the lack of a neuroprotective effect of aging on CA1 hippocampal neurons in aged male Wistar rats. This study determined and characterized the morphological damage to the CA1 area after 15 min of 4 VO in aged male Wistar rats, validating the use of this model in CI and aging research. |
Databáze: | OpenAIRE |
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