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Regulation of vascular endothelial genes by dietary flavonoids: structure-expression relationship studies and the role of the transcription factor KLF-2

机译:膳食类黄酮对血管内皮基因的调控:结构-表达关系研究和转录因子KLF-2的作用

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Physiological concentrations (1 mu M) of 15 flavonoids were evaluated in human umbilical vein endothelial cells in the presence of hydrogen peroxide (H2O2) for their ability to affect endothelial nitric oxide synthase (eNOS) and endothelin-1 (ET-1) expression in order to establish the structural basis of their bioactivity. Flavonoid effects on eNOS transcription factor Krupple like factor-2 (KLF-2) expression were also evaluated. All studied flavonoids appeared to be effective compounds for counteracting the oxidative stress-induced effects on vascular gene expression, indicating that flavonoids are an excellent source of functional endothelial regulator products. Notably, the more effective flavonoids for KLF-2 up-regulation resulted in the highest values for eNOS expression, showing that the increment of eNOS expression would take place through KLF-2 induction. Structure-activity relationship studies showed that the combinations of substructures on flavonoid skeleton that regulate eNOS expression are made up of the following elements: glycosylation and hydroxylation of C-ring, double bond C2=C3 at C-ring, methoxylation and hydroxylation of B-ring, ketone group in C4 at C-ring and glycosylation in C7 of A-ring, while flavonoid features involved in the reduction of vasoconstrictor ET-1 expression are as follows: double bond C2=C3 at C-ring glycosylation in C7 of A-ring and ketone group in C4 of C-ring. (C) 2015 Elsevier Inc. All rights reserved.
机译:在过氧化氢(H2O2)存在的条件下,在人脐静脉内皮细胞中评估了15种黄酮类化合物的生理浓度(1μM),以评估它们对内皮一氧化氮合酶(eNOS)和内皮素1(ET-1)表达的影响。以建立其生物活性的结构基础。还评估了类黄酮对eNOS转录因子Krupple like factor-2(KLF-2)表达的影响。所有研究过的类黄酮似乎都是有效的化合物,可抵消氧化应激诱导的对血管基因表达的影响,表明类黄酮是功能性内皮调节产物的极佳来源。值得注意的是,用于KLF-2上调的更有效的类黄酮导致eNOS表达的最高值,表明eNOS表达的增加将通过KLF-2诱导而发生。结构-活性关系研究表明,调节eNOS表达的类黄酮骨架上的亚结构组合由以下元素组成:C环的糖基化和羟基化,C环处的双键C2 = C3,B-的甲氧基化和羟基化环,C环上C4的酮基和A环C7的糖基化,而减少血管收缩剂ET-1表达的类黄酮特征如下:双键C2 = C3在A的C7的C环糖基化环和C环C4中的酮基。 (C)2015 Elsevier Inc.保留所有权利。

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