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Behav Brain Res ; 300: 11-24, 2016 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-26658515

RESUMO

The etiology of depression is unknown but has been associated with dysregulation of neuronal activity at numerous loci on the limbic-cortical circuitry. The Flinders Sensitive Line (FSL) is a validated rodent model of human depression with spontaneously emerging behavioral and physiological phenotype, however, the durability and robustness of the phenotypes have not been described. The objective of the current study was to evaluate longitudinal dynamics of the depressive-like symptoms in this animal model. FSL and control rats of both genders were assessed over 8 months, characterizing their performance at different time points on motor, sensorimotor and complex learning/memory based tasks. Changes over time in physiological parameters, such as corticosterone and blood glucose levels, were monitored. Regional glucose metabolism, used as a marker of neuronal activity, was assessed at different time points using F18-FDG Positron Emission Tomography (PET). Results show that certain deficits at 2-3 months--on tests such as the Elevated Plus Maze, Object Recognition, and the Forced Swim Test--were transitory and the phenotype was no longer present when re-testing at 6-7 months of age. However, a stable impairment was detected on a learning and memory task, particularly indicating dysfunction in retention of spatial information. Furthermore, at multiple time points, the PET scan indicated a significate bilateral, hypo-metabolism in the temporal lobes in the FSL rats compared to healthy controls. The data suggests possible alterations of entorhinal cortex metabolism concomitant with specific behavioral changes and supports the importance of understanding the dynamics and the time and gender dependence of the phenotypes present.


Assuntos
Transtorno Depressivo/diagnóstico por imagem , Transtorno Depressivo/fisiopatologia , Córtex Entorrinal/diagnóstico por imagem , Envelhecimento/fisiologia , Envelhecimento/psicologia , Animais , Mapeamento Encefálico , Corticosterona/sangue , Transtorno Depressivo/psicologia , Modelos Animais de Doenças , Córtex Entorrinal/fisiopatologia , Feminino , Fluordesoxiglucose F18 , Glucose/metabolismo , Deficiências da Aprendizagem/diagnóstico por imagem , Deficiências da Aprendizagem/fisiopatologia , Masculino , Aprendizagem em Labirinto , Transtornos da Memória/diagnóstico por imagem , Transtornos da Memória/fisiopatologia , Tomografia por Emissão de Pósitrons , Compostos Radiofarmacêuticos , Ratos , Reconhecimento Psicológico , Memória Espacial , Especificidade da Espécie
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