Crocus-derived compounds alter the aggregation pathway of Alzheimer’s Disease - associated beta amyloid protein

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Nikolaos Stavros Koulakiotis
Pasi Purhonen
Evangelos Gikas
Hans Hebert
Anthony Tsarbopoulos
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[1] The Goulandris Natural History Museum,GAIA Research Center, Bioanalytical Department
[2] KTH Royal Institute of Technology,School of Engineering Sciences in Chemistry, Biotechnology and Health, Department of Biomedical Engineering and Health Systems
[3] National and Kapodistrian University of Athens,Department of Pharmacy
[4] National and Kapodistrian University of Athens Medical School,Department of Pharmacology
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Natural products have played a dominant role in the discovery of lead compounds for the development of drugs aimed at the treatment of human diseases. This electrospray ionization-ion mobility spectrometry-mass spectrometry (ESI-IMS-MS)—based study demonstrates that dietary antioxidants, isolated components from the stigmas of saffron (Crocus sativus L.) may be effective in inhibiting Aβ fibrillogenesis, a neuropathological hallmark of Alzheimer’s Disease (AD). This study reveals a substantial alteration in the monomer/oligomer distribution of Aβ1-40, concomitant with re-direction of fibril formation, induced by the natural product interaction. These alterations on the Aβ1-40 aggregation pathway are most prominent for trans-crocin-4 (TC4). Use of ESI-IMS-MS, electron microscopy alongside Thioflavin-T kinetics, and the interpretation of 3-dimensional Driftscope plots indicate a correlation of these monomer/oligomer distribution changes with alterations to Aβ1-40 amyloid formation. The latter could prove instrumental in the development of novel aggregation inhibitors for the prevention, or treatment of AD.
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