Cannabidiol Inhibits Tau Aggregation In Vitro

被引:22
作者
Alali, Soha [1 ]
Riazi, Gholamhossein [1 ]
Ashrafi-Kooshk, Mohammad Reza [1 ]
Meknatkhah, Sogol [1 ]
Ahmadian, Shahin [2 ]
Hooshyari Ardakani, Mohammad [3 ]
Hosseinkhani, Baharak [4 ]
机构
[1] Univ Tehran, Inst Biochem & Biophys IBB, Lab Neuroorgan Chem, Tehran 1417614335, Iran
[2] Univ Tehran, Inst Biochem & Biophys, Dept Biochem, Tehran 1417614335, Iran
[3] Shahid Beheshti Univ, Med Plants & Drugs Res Inst, Dept Phytochem, GC, Tehran 1983969411, Iran
[4] Hasselt Univ, Biomed Res Inst BIOMED, Martelarenlaan 42, B-3500 Hasselt, Belgium
关键词
Alzheimer's disease; tau protein; amyloid fibrils; cannabidiol; OXIDATIVE STRESS; PPAR-GAMMA; PROTEIN; BINDING; EXPRESSION; PEPTIDE; PATHWAY; RESIDUE; LENGTH;
D O I
10.3390/cells10123521
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A hallmark of Alzheimer's disease (AD) is the accumulation of tau protein in the brain. Compelling evidence indicates that the presence of tau aggregates causes irreversible neuronal destruction, eventually leading to synaptic loss. So far, the inhibition of tau aggregation has been recognized as one of the most effective therapeutic strategies. Cannabidiol (CBD), a major component found in Cannabis sativa L., has antioxidant activities as well as numerous neuroprotective features. Therefore, we hypothesize that CBD may serve as a potent substance to hamper tau aggregation in AD. In this study, we aim to investigate the CBD effect on the aggregation of recombinant human tau protein 1N/4R isoform using biochemical methods in vitro and in silico. Using Thioflavin T (ThT) assay, circular dichroism (CD), and atomic force microscopy (AFM), we demonstrated that CBD can suppress tau fibrils formation. Moreover, by quenching assay, docking, and job's plot, we further demonstrated that one molecule of CBD interacts with one molecule of tau protein through a spontaneous binding. Experiments performed by quenching assay, docking, and Thioflavin T assay further established that the main forces are hydrogen Van der Waals and some non-negligible hydrophobic forces, affecting the lag phase of tau protein kinetics. Taken together, this study provides new insights about a natural substance, CBD, for tau therapy which may offer new hope for the treatment of AD.
引用
收藏
页数:19
相关论文
共 47 条
[41]   WATER CLUSTERS - CONTRIBUTIONS OF BINDING-ENERGY AND ENTROPY TO STABILITY [J].
SHI, Z ;
FORD, JV ;
WEI, S ;
CASTLEMAN, AW .
JOURNAL OF CHEMICAL PHYSICS, 1993, 99 (10) :8009-8015
[42]   Structural impact of heparin binding to full-length Tau as studied by NMR spectroscopy [J].
Sibille, Nathalie ;
Sillen, Alain ;
Leroy, Arnaud ;
Wieruszeski, Jean-Michel ;
Mulloy, Barbara ;
Landrieu, Isabelle ;
Lippens, Guy .
BIOCHEMISTRY, 2006, 45 (41) :12560-12572
[43]   Interaction of caffeine and sulfadiazine with lysozyme adsorbed at colloidal metal nanoparticle interface: influence on drug transport ability and antibacterial activity [J].
Sonu, Vikash K. ;
Rajkumar, Imocha ;
Bhattacharjee, Kaushik ;
Joshi, S. R. ;
Mitra, Sivaprasad .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2019, 37 (02) :321-335
[44]   Synthesis and spectroscopic characterization of 4-butoxyethoxy-N-octadecyl-1,8-naphthalimide as a new fluorescent probe for the determination of proteins [J].
Sun, Yang ;
Wei, Song ;
Yin, Chen ;
Liu, Lusha ;
Hu, Chunmei ;
Zhao, Yingyong ;
Ye, Yanxi ;
Hu, Xiaoyun ;
Fan, Jun .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (12) :3798-3804
[45]   Effects of cannabidiol interactions with Wnt/β-catenin pathway and PPARγ on oxidative stress and neuroinflammation in Alzheimer's disease [J].
Vallee, Alexandre ;
Lecarpentier, Yves ;
Guillevin, Remy ;
Vallee, Jean-Noel .
ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2017, 49 (10) :853-866
[46]   The core of tau-paired helical filaments studied by scanning transmission electron microscopy and limited proteolysis [J].
von Bergen, Martin ;
Barghorn, Stefan ;
Mueller, Shirley A. ;
Pickhardt, Marcus ;
Biernat, Jacek ;
Mandelkow, Eva-Maria ;
Davies, Peter ;
Aebi, Ueli ;
Mandelkow, Eckhard .
BIOCHEMISTRY, 2006, 45 (20) :6446-6457
[47]   Selective inhibition of Alzheimer disease-like tau aggregation by phenothiazines [J].
Wischik, CM ;
Edwards, PC ;
Lai, RYK ;
Roth, M ;
Harrington, CR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) :11213-11218