Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Andrade, Víctora; b | Cortés, Nicolea; b | Pastor, Gabrielaa; b; c | Gonzalez, Andreaa; b | Ramos-Escobar, Nicolása; b | Pastene, Edgard | Rojo, Leonel E.c; * | Maccioni, Ricardo B.a; b; *
Affiliations: [a] International Center for Biomedicine (ICC), Santiago, Chile | [b] Laboratory of Neurosciences and Functional Medicine, Faculty of Sciences, University of Chile, Santiago, Chile | [c] Departamento de Biología, Facultad de Química y Biología, Universidad de Santiago de Chile, Santiago, Chile | [d] Departamento de Farmacia, Universidad de Concepción, Concepción, Chile
Correspondence: [*] Correspondence to: Dr. Ricardo B. Maccioni, International Center for Biomedicine, Avda. Vitacura 3568. D511, Vitacura, Santiago, Chile. [email protected]; Dr. Leonel E. Rojo, Departamento de Biología, Facultad de Química y Biología, Universidad de Santiago de Chile, Santiago, Chile. [email protected]
Abstract: Background:Alzheimer’s disease (AD) is a multifactorial disease, that involves neuroinflammatory processes in which microglial cells respond to “damage signals”. The latter includes oligomeric tau, iron, oxidative free radicals, and other molecules that promotes neuroinflammation in the brain, promoting neuronal death and cognitive impairment. Since AD is the first cause of dementia in the elderly, and its pharmacotherapy has limited efficacy, novel treatments are critical to improve the quality of life of AD patients. Multitarget therapy based on nutraceuticals has been proposed as a promising intervention based on evidence from clinical trials. Several studies have shown that epicatechin-derived polyphenols from tea improve cognitive performance; also, the polyphenol molecule N-acetylcysteine (NAC) promotes neuroprotection. Objective:To develop an approach for a rational design of leading compounds against AD, based on specific semisynthetic epicatechin and catechin derivatives. Methods:We evaluated tau aggregation in vitro and neuritogenesis by confocal microscopy in mouse neuroblastoma cells (N2a), after exposing cells to either epicatechin-pyrogallol (EPIC-PYR), catechin-pyrogallol (CAT-PYR), catechin-phloroglucinol (CAT-PhG), and NAC. Results:We found that EPIC-PYR, CAT-PYR, and CAT-PhG inhibit human tau aggregation and significantly increase neuritogenesis in a dose-dependent manner. Interestingly, modification with a phloroglucinol group yielded the most potent molecule of those evaluated, suggesting that the phloroglucinol group may enhance neuroprotective activity of the catechin-derived compounds. Also, as observed with cathechins, NAC promotes neuritogenesis and inhibits tau self-aggregation, possibly through a different pathway. Conclusion:EPIC-PYR, CAT-PYR, CAT-PhG, and NAC increased the number of neurites in Na2 cell line and inhibits tau-self aggregation in vitro.
Keywords: Alzheimer’s disease, bioactive compounds, molecular functions, molecular networks, natural compounds, polyphenols, prevalent neurological disorders, tau oligomerization
DOI: 10.3233/JAD-200067
Journal: Journal of Alzheimer's Disease, vol. 75, no. 4, pp. 1219-1227, 2020
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
[email protected]
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office [email protected]
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
如果您在出版方面需要帮助或有任何建, 件至: [email protected]