Inhibitory Activities of Propolis and Its Promising Component, Caffeic Acid Phenethyl Ester, against Amyloidogenesis of Human Transthyretin

被引:42
|
作者
Yokoyama, Takeshi [1 ]
Kosaka, Yuto [1 ]
Mizuguchi, Mineyuld [1 ]
机构
[1] Toyama Univ, Fac Pharmaceut Sci, Toyama 9300914, Japan
关键词
AMYLOID FIBRIL INHIBITORS; X-RAY-DIFFRACTION; POTENT; BINDING; PROTEIN; VARIANT; SERUM; POLYNEUROPATHY; DENATURATION; CYCLODEXTRIN;
D O I
10.1021/jm500997m
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Transthyretin (TTR) is a homotetrameric serum protein associated with amyloidoses such as familial amyloid polyneuropathy and senile systemic amyloidosis. The amyloid fibril formation of TTR can be inhibited through stabilization of the TTR tetramer by the binding of small molecules. In this study, we examined the inhibitory potency of caffeic acid phenethyl ester (CAPE) and its derivatives. Thioflavin T assay showed that CAPE suppressed the amyloid fibril formation of TTR. Comparative analysis of the inhibitory potencies revealed that phenethyl ferulate was the most potent among the CAPE derivatives. The binding of phenethyl ferulate and the selected compounds to TTR were confirmed by the 8-anilino-1-naphthalenesulfonic acid displacement and X-ray crystallography. It was also demonstrated that Bio 30, which is a CAPE-rich commercially available New Zealand propolis, inhibited TTR amyloidogenesis and stabilized the TTR tetramer. These results suggested that a propolis may be efficient for preventing TTR amyloidosis.
引用
收藏
页码:8928 / 8935
页数:8
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