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Publication : Short amylin receptor antagonist peptides improve memory deficits in Alzheimer's disease mouse model.

First Author  Soudy R Year  2019
Journal  Sci Rep Volume  9
Issue  1 Pages  10942
PubMed ID  31358858 Mgi Jnum  J:284802
Mgi Id  MGI:6387509 Doi  10.1038/s41598-019-47255-9
Citation  Soudy R, et al. (2019) Short amylin receptor antagonist peptides improve memory deficits in Alzheimer's disease mouse model. Sci Rep 9(1):10942
abstractText  Recent evidence supports involvement of amylin and the amylin receptor in the pathogenesis of Alzheimer's disease (AD). We have previously shown that amylin receptor antagonist, AC253, improves spatial memory in AD mouse models. Herein, we generated and screened a peptide library and identified two short sequence amylin peptides (12-14 aa) that are proteolytically stable, brain penetrant when administered intraperitoneally, neuroprotective against Abeta toxicity and restore diminished levels of hippocampal long term potentiation in AD mice. Systemic administration of the peptides for five weeks in aged 5XFAD mice improved spatial memory, reduced amyloid plaque burden, and neuroinflammation. The common residue SQELHRLQTY within the peptides is an essential sequence for preservation of the beneficial effects of the fragments that we report here and constitutes a new pharmacological target. These findings suggest that the amylin receptor antagonism may represent a novel therapy for AD.
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