P1-105: In vitro Characterization of Fibrillar Amyloid, TAU Deposition, and Activated Astrocytes in Arctic Alzheimer's Disease Brain in Comparison With Sporadic Alzheimer's Disease Brain Using 3H-PIB, 3H-THK5117 and 3H-DEPRENYL

2016 ◽  
Vol 12 ◽  
pp. P442-P442
Author(s):  
Laetitia Lemoine ◽  
Martin Ingelsson ◽  
Inger Nennesmo ◽  
Per-Goran Gillberg ◽  
Agneta Nordberg
2013 ◽  
Vol 9 ◽  
pp. P101-P101
Author(s):  
Tsing-Bau Chen ◽  
Zhizhen Zeng ◽  
Patricia Miller ◽  
Stacey O'Malley ◽  
Brett Connolly ◽  
...  

2013 ◽  
Vol 9 ◽  
pp. P260-P260
Author(s):  
Zhizhen Zeng ◽  
Tsing-Bau Chen ◽  
Patricia Miller ◽  
Stacey O'Malley ◽  
Brett Connolly ◽  
...  

2013 ◽  
Vol 1830 (4) ◽  
pp. 2960-2969 ◽  
Author(s):  
Pham Dinh Quoc Huy ◽  
Yao-Chung Yu ◽  
Son Tung Ngo ◽  
Tran Van Thao ◽  
Chin-piao Chen ◽  
...  

2015 ◽  
Vol 11 (7S_Part_19) ◽  
pp. P878-P878
Author(s):  
Ruiqing Ni ◽  
Per-Göran Gillberg ◽  
Matti Viitanen ◽  
Liisa Myllykangas ◽  
Nenad Bogdanovic ◽  
...  

2020 ◽  
Vol 19 ◽  
Author(s):  
Maja Przybyłowska ◽  
Krystyna Dzierzbicka ◽  
Szymon Kowalski ◽  
Klaudia Chmielewska ◽  
Iwona Inkielewicz-Stepniak

: The aim of this work is review of tacrine analogues from the last three years, which were not included in the latest review work, donepezil and galantamine hybrids from 2015 and rivastigmine derivatives from 2014. In this account we summarize the efforts toward the development and characterization of non-toxic inhibitors of cholinesterases based on mentioned drugs with various interesting additional properties such as antioxidant, decreasing β-amyloid plaque aggregation, nitric oxide production, pro-inflammatory cytokines release, monoamine oxidase-B activity, cytotoxicity and oxidative stress in vitro and in animal model that classify these hybrids as potential multifunctional therapeutic agents for Alzheimer’s disease. Moreover, herein, we have described the cholinergic hypothesis, mechanisms of neurodegeneration and current pharmacotherapy of Alzheimer’s disease which is based on the restoration of cholinergic function through blocking enzymes that break down acetylcholine.


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