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Epigallocatechin Gallate Decreases the Micellar Solubility of Cholesterol via Specific Interaction with Phosphatidylcholine

机译:表没食子儿茶素没食子酸酯通过与磷脂酰胆碱的特异性相互作用降低胆固醇的胶束溶解度

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The mechanisms underlying the effect of epigallocatechin gallate (EGCG) on the micellar solubility of cholesterol were examined. EGCG eliminated both cholesterol and phosphatidylcholine (PC) from bile salt micelles in a dose-dependent manner in vitro. When the bile salt micelles contained a phospholipid other than PC, neither cholesterol nor the phospholipid was eliminated following the addition of EGCG. When vesicles comprised of various phospholipids were prepared and, EGCG was added to the vesicles, EGCG effectively and exclusively eliminated only PC. An intermolecular nuclear Overhauser effect (NOE) was observed between PC and EGCG in bile salt micelles with EGCG added, but not between cholesterol and EGCG, by using a NOE-correlated spectroscopy nuclear magnetic resonance method. The results of binding analyses using surface plasmon resonance (SPR) showed that EGCG did not bind to cholesterol. These observations strongly suggest that EGCG decreases the micellar solubility of cholesterol via specific interaction with PC.
机译:考察了表没食子儿茶素没食子酸酯(EGCG)对胆固醇的胶束溶解度的影响的潜在机制。 EGCG在体外以剂量依赖性方式消除了胆汁盐微团中的胆固醇和磷脂酰胆碱(PC)。当胆汁盐胶束包含除PC以外的磷脂时,添加EGCG后胆固醇和磷脂都不会被清除。当制备由各种磷脂组成的囊泡并将EGCG添加到囊泡中时,EGCG有效且仅消除了PC。通过使用NOE相关光谱核磁共振方法,在添加了EGCG的胆盐胶束中,在PC和EGCG之间观察到了分子间核Overhauser效应(NOE),但在胆固醇和EGCG之间未观察到分子间的核Overhauser效应。使用表面等离子体共振(SPR)的结合分析结果表明,EGCG不与胆固醇结合。这些观察结果强烈表明,EGCG通过与PC的特异性相互作用降低了胆固醇的胶束溶解度。

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