Grape Derived Polyphenols Attenuate Tau Neuropathology in a Mouse Model of Alzheimer's Disease

被引:104
|
作者
Wang, Jun [1 ,2 ]
Santa-Maria, Ismael [1 ,2 ,3 ]
Ho, Lap [1 ,2 ,4 ]
Ksiezak-Reding, Hanna [1 ,2 ,4 ]
Ono, Kenjiro [5 ,6 ,7 ,8 ]
Teplow, David B. [6 ,7 ,8 ]
Pasinetti, Giulio Maria [1 ,2 ,4 ]
机构
[1] Mt Sinai Sch Med, Dept Neurol, New York, NY 10029 USA
[2] Mt Sinai Sch Med, Dept Psychiat, New York, NY 10029 USA
[3] Queen Sofia Fdn, CIEN Fdn, Alzheimer Dis Res Unit, Madrid, Spain
[4] James J Peters Affairs Med Ctr, Geriatr Res Educ & Clin Ctr, Bronx, NY USA
[5] Kanazawa Univ, Grad Sch Med Sci, Takara Machi, Kanazawa, Japan
[6] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
[7] Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA 90024 USA
[8] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90024 USA
关键词
Aggregation; Alzheimer's disease; hyperphosphorylation; neurofibrillary tangles; tauopathies; PAIRED HELICAL FILAMENTS; BETA-STRUCTURE; IN-VITRO; PROTEIN; KINASE; PHOSPHORYLATION; SEED; ERK2; LOCALIZATION; MICROTUBULES;
D O I
10.3233/JAD-2010-101074
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:653 / 661
页数:9
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