| Literature DB >> 22778851 |
Susanne Aileen Funke1, Thomas van Groen, Inga Kadish, Dirk Bartnik, Luitgard Nagel-Steger, Oleksandr Brener, Torsten Sehl, Renu Batra-Safferling, Christine Moriscot, Guy Schoehn, Anselm H C Horn, Andreas Müller-Schiffmann, Carsten Korth, Heinrich Sticht, Dieter Willbold.
Abstract
Several lines of evidence suggest that the amyloid-β-peptide (Aβ) plays a central role in the pathogenesis of Alzheimer's disease (AD). Not only Aβ fibrils but also small soluble Aβ oligomers in particular are suspected to be the major toxic species responsible for disease development and progression. The present study reports on in vitro and in vivo properties of the Aβ targeting d-enantiomeric amino acid peptide D3. We show that next to plaque load and inflammation reduction, oral application of the peptide improved the cognitive performance of AD transgenic mice. In addition, we provide in vitro data elucidating the potential mechanism underlying the observed in vivo activity of D3. These data suggest that D3 precipitates toxic Aβ species and converts them into nonamyloidogenic, nonfibrillar, and nontoxic aggregates without increasing the concentration of monomeric Aβ. Thus, D3 exerts an interesting and novel mechanism of action that abolishes toxic Aβ oligomers and thereby supports their decisive role in AD development and progression.Entities:
Keywords: Alzheimer’s disease; Mirror image phage display; d-enantiomeric peptide; drugs; oligomers
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Year: 2010 PMID: 22778851 PMCID: PMC3368690 DOI: 10.1021/cn100057j
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418