期刊
BIOCHEMISTRY
卷 57, 期 8, 页码 1399-1409出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.biochem.7b01214
关键词
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资金
- Alzheimer's Drug Discovery Foundation
- Robertson Therapeutic Development Fund for H.A., NIH [NS50537]
- Tri-Institutional Therapeutics Discovery Institute
- Rudin Family Foundation
- John A. Herrmann
Accumulating evidence suggests that fibrinogen, a key protein in the coagulation cascade, plays an important role in circulatory dysfunction in Alzheimer's disease (AD). Previous work has shown that the interaction between fibrinogen and beta-amyloid (A beta), a hallmark pathological protein in AD, induces plasmin-resistant abnormal blood clots, delays fibrinolysis, increases inflammation, and aggravates cognitive function in mouse models of AD. Since A beta oligomers have a much stronger affinity for fibrinogen than A beta monomers, we tested whether amyloid aggregation inhibitors could block the A beta-fibrinogen interaction and found that some A beta aggregation inhibitors showed moderate inhibitory efficacy against this interaction. We then modified a hit compound so that it not only showed a strong inhibitory efficacy toward the A beta-fibrinogen interaction but also retained its potency toward the A beta 42 aggregation inhibition process. Furthermore, our best hit compound, TDI-2760, modulated A beta 42-induced contact system activation, a pathological condition observed in some AD patients, in addition to inhibiting the A beta-fibrinogen interaction and A beta-aggregation. Thus, TDI-2760 has the potential to lessen vascular abnormalities as well as A beta aggregation-driven pathology in AD.
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