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Beta-secretase inhibitor GRL-8234 rescues age-related cognitive decline in APP transgenic mice.


ABSTRACT: Alzheimer disease is intimately linked to an excess amount of amyloid-? (A?) in the brain. Thus, therapeutic inhibition of A? production is an attractive clinical approach to treat this disease. Here we provide the first direct experimental evidence that the treatment of Tg2576 transgenic mice with an inhibitor of ?-secretase, GRL-8234, rescues the age-related cognitive decline. We demonstrated that the injected GRL-8234 effectively enters the brain and rapidly decreases soluble A? in the brain of Tg2576 mice. The rescue of cognition, which was observed only after long-term inhibitor treatment ranging from 5 to 7.5 mo, was associated with a decrease of brain amyloid-? plaque load. We also found no accumulation of amyloid-? precursor protein after several months of inhibitor treatment. These observations substantiate the idea that A? accumulation plays a major role in the cognitive decline of Tg2576 mice and support the concept of A? reduction therapy as a treatment of AD.

SUBMITTER: Chang WP 

PROVIDER: S-EPMC3023390 | biostudies-literature | 2011 Feb

REPOSITORIES: biostudies-literature

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Beta-secretase inhibitor GRL-8234 rescues age-related cognitive decline in APP transgenic mice.

Chang Wan-Pin WP   Huang Xiangping X   Downs Deborah D   Cirrito John R JR   Koelsch Gerald G   Holtzman David M DM   Ghosh Arun K AK   Tang Jordan J  

FASEB journal : official publication of the Federation of American Societies for Experimental Biology 20101108 2


Alzheimer disease is intimately linked to an excess amount of amyloid-β (Aβ) in the brain. Thus, therapeutic inhibition of Aβ production is an attractive clinical approach to treat this disease. Here we provide the first direct experimental evidence that the treatment of Tg2576 transgenic mice with an inhibitor of β-secretase, GRL-8234, rescues the age-related cognitive decline. We demonstrated that the injected GRL-8234 effectively enters the brain and rapidly decreases soluble Aβ in the brain  ...[more]

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