Abstract
Ligands of the translocator protein (TSPO) elicit pleiotropic neuroprotective effects that represent emerging treatment strategies for several neurodegenerative conditions. To investigate the potential of TSPO as a therapeutic target for Alzheimer's disease (AD), the current study assessed the effects of the TSPO ligand Ro5-4864 on the development of neuropathology in 3xTgAD mice. The effects of the TSPO ligand on neurosteroidogenesis and AD-related neuropathology, including β-amyloid accumulation, gliosis, and behavioral impairment, were examined under both early intervention (7-month-old young-adult male mice with low pathology) and treatment (24- month-old, aged male mice with advanced neuropathology) conditions. Ro5-4864 treatment not only effectively attenuated development of neuropathology and behavioral impairment in young-adult mice but also reversed these indices in aged 3xTgAD mice. Reduced levels of soluble β-amyloid were also observed by the combination of TSPO ligands Ro5-4864 and PK11195 in nontransgenicmice.ThesefindingssuggestthatTSPOisapromisingtargetforthedevelopmentofpleiotropictreatmentstrategies for the management of AD. © 2013 the authors.
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CITATION STYLE
Barron, A. M., Garcia-Segura, L. M., Caruso, D., Jayaraman, A., Lee, J. W., Melcangi, R. C., & Pike, C. J. (2013). Ligand for translocator protein reverses pathology in a mouse model of Alzheimer’s disease. Journal of Neuroscience, 33(20), 8891–8897. https://doi.org/10.1523/JNEUROSCI.1350-13.2013
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