TY - JOUR
T1 - Grape derived polyphenols attenuate Tau neuropathology in a mouse model of alzheimer's disease
AU - Wang, Jun
AU - Santa-Maria, Ismael
AU - Ho, Lap
AU - Ksiezak-Reding, Hanna
AU - Ono, Kenjiro
AU - Teplow, David B.
AU - Pasinetti, Giulio Maria
PY - 2010
Y1 - 2010
N2 - Aggregation of microtubule-associated protein tau into insoluble intracellular neurofibrillary tangles is a characteristic hallmark of Alzheimer's disease (AD) and other neurodegenerative diseases, including progressive supranuclear palsy, argyrophilic grain disease, corticobasal degeneration, frontotemporal dementias with Parkinsonism linked to chromosome 17, and Pick's disease. Tau is abnormally hyperphosphorylated in AD and aberrant tau phosphorylation contributes to the neuropathology of AD and other tauopathies. Anti-aggregation and anti-phosphorylation are main approaches for tau-based therapy. In this study, we report that a select grape-seed polyphenol extract (GSPE) could potently interfere with the assembly of tau peptides into neurotoxic aggregates. Moreover, oral administration of GSPE significantly attenuated the development of AD type tau neuropathology in the brain of TMHT mouse model of AD through mechanisms associated with attenuation of extracellular signal-receptor kinase 1/2 signaling in the brain.
AB - Aggregation of microtubule-associated protein tau into insoluble intracellular neurofibrillary tangles is a characteristic hallmark of Alzheimer's disease (AD) and other neurodegenerative diseases, including progressive supranuclear palsy, argyrophilic grain disease, corticobasal degeneration, frontotemporal dementias with Parkinsonism linked to chromosome 17, and Pick's disease. Tau is abnormally hyperphosphorylated in AD and aberrant tau phosphorylation contributes to the neuropathology of AD and other tauopathies. Anti-aggregation and anti-phosphorylation are main approaches for tau-based therapy. In this study, we report that a select grape-seed polyphenol extract (GSPE) could potently interfere with the assembly of tau peptides into neurotoxic aggregates. Moreover, oral administration of GSPE significantly attenuated the development of AD type tau neuropathology in the brain of TMHT mouse model of AD through mechanisms associated with attenuation of extracellular signal-receptor kinase 1/2 signaling in the brain.
KW - Aggregation
KW - Alzheimer's disease
KW - hyperphosphorylation
KW - neurofibrillary tangles
KW - tauopathies
UR - http://www.scopus.com/inward/record.url?scp=78650816787&partnerID=8YFLogxK
U2 - 10.3233/JAD-2010-101074
DO - 10.3233/JAD-2010-101074
M3 - Article
AN - SCOPUS:78650816787
SN - 1387-2877
VL - 22
SP - 653
EP - 661
JO - Journal of Alzheimer's Disease
JF - Journal of Alzheimer's Disease
IS - 2
ER -