Rosiglitazone Rescues Memory Impairment in Alzheimer's Transgenic Mice: Mechanisms Involving a Reduced Amyloid and Tau Pathology

Clinical studies suggest that agonists at peroxisome proliferator-activated receptor gamma (PPARγ) may exert beneficial effects in patients with mild-to-moderate Alzheimer's disease (AD), but the mechanism for the potential therapeutic interest of this class of drugs has not yet been elucidated...

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Detalles Bibliográficos
Autores: Escribano, L. (Luis)|||/items/649f5ff2-0bec-4c20-936b-9876dd0e11d8, Simon, A.M. (Ana María)|||/items/50808fdd-b9b9-461c-a7a5-e22a36ed24c2, Gimeno, E. (Esther)|||/items/4e87ba86-99e7-4620-870b-4827ad33da81, Cuadrado-Tejedor, M. (Mar)|||/items/8e19b277-1821-4ae8-9617-975de11dbdd1, Lopez-de-Maturana, R. (Raquel)|||/items/62cbd059-b452-4292-9fea-4ff88e9079d3, Garcia-Osta, A. (Ana)|||/items/6a828922-d55a-4aca-9dec-ccfb2a7380f8, Ricobaraza, A. (Ana)|||/items/a537e067-03df-4041-b520-0d8a5bd924ab, Perez-Mediavilla, L.A. (Luis Alberto)|||/items/276fc9af-5d47-49eb-bf67-6d35fc210186, Rio, J. (Joaquín) del|||/items/c65d5fe5-1ba6-4689-915c-e793a125a0a3, Frechilla, D. (Diana)|||/items/7d1f0c54-3eb7-4b6c-a749-c586ca5f0caf
Tipo de recurso: artículo
Fecha de publicación:2010
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/12953
Acceso en línea:https://hdl.handle.net/10171/12953
Access Level:acceso abierto
Palabra clave:Alzheimer's disease
amyloid
tau
PPARγ
hippocampus
memory
Descripción
Sumario:Clinical studies suggest that agonists at peroxisome proliferator-activated receptor gamma (PPARγ) may exert beneficial effects in patients with mild-to-moderate Alzheimer's disease (AD), but the mechanism for the potential therapeutic interest of this class of drugs has not yet been elucidated. Here, in mice overexpressing mutant human amyloid precursor protein, we found that chronic treatment with rosiglitazone, a high-affinity agonist at PPARγ, facilitated β-amyloid peptide (Aβ) clearance. Rosiglitazone not only reduced Aβ burden in the brain but, importantly, almost completely removed the abundant amyloid plaques observed in the hippocampus and entorhinal cortex of 13-month-old transgenic mice. In the hippocampus, neuropil threads containing phosphorylated tau, probably corresponding to dystrophic neurites, were also decreased by the drug. Rosiglitazone switched on the activated microglial phenotype, promoting its phagocytic ability, reducing the expression of proinflammatory markers and inducing factors for alternative differentiation. The decreased amyloid pathology may account for the reduction of p-tau-containing neuropil threads and for the rescue of impaired recognition and spatial memory in the transgenic mice. This study provides further insights into the mechanisms for the beneficial effect of rosiglitazone in AD patients.