Protocatechuic Acid: Inhibition of Fibril Formation, Destabilization of Preformed Fibrils of Amyloid-β and α-Synuclein, and Neuroprotection

被引:69
作者
Hornedo-Ortega, Ruth [1 ]
Antonia Alvarez-Fernandez, Maria [1 ]
Belen Cerezo, Ana [1 ]
Richard, Tristan [2 ]
Maria Troncoso, Ana [1 ]
Carmen Garcia-Parrilla, Maria [1 ]
机构
[1] Univ Seville, Fac Pharm, Area Nutr & Food Sci, C-P Garcia Gonzalez 2, E-41012 Seville, Spain
[2] Univ Bordeaux, ISVV Bordeaux Aquitaine, 71 Ave Edouard Bourleaux, F-33883 Villenave Dornon, France
关键词
neurodegeneration; toxicity; protocatechuic acid; amyloid-beta; alpha-synuclein; CYANIDIN; 3-O-GLUCOPYRANOSIDE; IN-VITRO; ANTHOCYANINS; METABOLISM; ABSORPTION; PHARMACOKINETICS; CONSUMPTION; PHENOLICS; PROTECTS;
D O I
10.1021/acs.jafc.6b03217
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Protocatechuic acid (PCA) is the major metabolite of the anthocyanin known as cyanidin 3-glucoside. It is found in plasma and tissues, such as the brain, heart, liver, and kidneys, following consumption of a rich source of this flavonoid. The abnormal pathological assembly of amyloid-beta (A beta) and alpha-synuclein (alpha S) is an underlying mechanism involved in the formation of amyloid plaques and Lewy bodies in the brain, which are responsible for neuropathology symptoms in Alzheimer's (AD) and Parkinson's diseases (PD), respectively. This research was performed to evaluate the protective effects of PCA, by establishing its potential role in inhibiting aggregation and fibril destabilization of A beta and alpha S proteins. It has been found that PCA inhibits the aggregation of A beta and alpha S and destabilizes their preformed fibrils. These results were confirmed by TEM images, electrophoresis, and immunoblotting experiments. Furthermore, PCA prevents the death of PC12 cells triggered by A beta- and alpha S-induced toxicity.
引用
收藏
页码:7722 / 7732
页数:11
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