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J Alzheimers Dis
; 46(4): 849-53, 2015.
Article
in English
| MEDLINE
| ID: mdl-26402624
ABSTRACT
Two tetrapeptides, HAEE and RADD, which are ionic-complementary to the primary zinc recognition site of amyloid-ß (Aß), have been reported to inhibit zinc-induced dimerization of the Aß metal-binding domain and slow Aß aggregation in vitro. In the present study, we investigate the impact of HAEE and RADD on the development of cerebral ß-amyloidosis in a mouse model of Alzheimer's disease. We have found chronic intravenous administration of each peptide results in significant decrease of amyloid plaque burden in the treated mice.