Coumarin derivatives against amyloid-beta 40 - 42 peptide and tau protein

被引:1
作者
Kowalczyk, Joanna [1 ]
Skalicka-Wozniak, Krystyna [2 ]
Budzynska, Barbara [1 ]
El Sayed, Nesrine [3 ]
Espargaro, Alba [4 ,5 ]
Sabate, Raimon [4 ,5 ]
机构
[1] Med Univ Lublin, Independent Lab Behav Studies, Jaczewskiego 4, PL-20090 Lublin, Poland
[2] Med Univ Lublin, Dept Nat Prod Chem, 1 Chodzki St, PL-20093 Lublin, Poland
[3] Cairo Univ, Dept Pharmacol & Toxicol, Cairo, Egypt
[4] Univ Barcelona, Dept Pharm & Pharmaceut Technol & Phys Chem, Barcelona, Catalonia, Spain
[5] Univ Barcelona, Inst Nanosci & Nanotechnol IN2UB, Barcelona, Catalonia, Spain
关键词
neurodegeneration; tau; A beta 40/42; in vitro; in cellulo; coumarins; ALZHEIMERS-DISEASE; LIGANDS;
D O I
10.2478/cipms-2022-0013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In preclinical studies, simple coumarins (scoparone, limettin) and furanocoumarins (imperatorin, xanthotoxin, bergapten) have already found to demonstrate procognitive abilities. 'Ibis suggests that they hold antioxidative, anti-inflammatory and inhibitory action towards acetylcholinesterase activities. However, little is known about their influence on the amyloidal structure formation, the leading cause of Alzheimer's disease (AD). In vitro and in cellulo assays were applied to evaluate the effect of selected coumarins on the different stages of A beta 40/42 and tau protein aggregation. Kinetic analyses were performed to evaluate their inhibiting abilities in time. Limettin revealed the most potent inhibiting profile towards A beta 40 aggregation, however, all tested compounds presented low influence on A beta 42 and tau protein aggregation inhibition. Despite the preliminary stage of the project, the promising effects of coumarins on A beta 40 aggregation were shown. This suggests the coumarin scaffold can serve as a potential multitarget agent in AD treatment, but further studies are required to confirm this.
引用
收藏
页码:67 / 74
页数:8
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