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Strong activation of cyclooxygenase I and II catalytic activity by dietary bioflavonoids

机译:膳食生物类黄酮强烈激活环氧合酶I和II的催化活性

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摘要

Cyclooxygenases (COXs) catalyze the conversion of arachidonic acid to prostaglandins (PGs), thromboxanes, and hydroxyeicosatetraenoic acids. In the present study, we investigated several dietary bioflavonoids for their ability to modulate the catalytic activity of COX I and II in vitro and also in cultured cells. We found that some of them are the most powerful direct stimulators of the catalytic activity of COX I and II known to date, increasing the formation of prostaglandin products in vitro by up to 11-fold over the controls. This stimulatory effect of bioflavonoids is enzyme specific because none of them stimulates the catalytic activity of a number of lipooxygenases tested. Compared with phenol, a prototypical COX stimulator commonly used in vitro, the naturally occurring bioflavonoids are up to 29 times more efficacious in stimulating the COX activity. Additional studies using intact cells in culture showed that some of the dietary compounds that were active in the biochemical assays also activated the formation of PGE2 (a representative PG) when they were present at 0.01 to 1 μM concentrations. The stimulatory effect of dietary compounds on COX-mediated PG formation is far more potent in intact cells than in the in vitro assays. Mechanistically, bioflavonoids mainly acted to slow down the suicidal inactivation of the COX enzymes, but they did not appear to reactivate the inactivated enzymes. The finding of this study suggests that some of the bioflavonoids likely will serve as the naturally occurring cofactors for the COX enzymes in humans.
机译:环氧合酶(COXs)催化花生四烯酸向前列腺素(PGs),血栓烷和羟基二十碳四烯酸的转化。在本研究中,我们研究了几种膳食生物类黄酮在体外以及在培养细胞中调节COX I和II催化活性的能力。我们发现其中一些是迄今为止已知的COX I和II催化活性的最强大的直接刺激剂,与体外对照相比,体外增加的前列腺素产品的形成增加了11倍。生物类黄酮的这种刺激作用是酶特异性的,因为它们都没有刺激多种测试的脂加氧酶的催化活性。与苯酚(一种通常在体外使用的典型COX刺激物)相比,天然存在的生物类黄酮在刺激COX活性方面的功效高达29倍。使用完整细胞进行培养的其他研究表明,某些生化分析中具有活性的膳食化合物以0.01至1μM的浓度存在时,也会激活PGE2(代表性的PG)的形成。与完整的细胞相比,膳食化合物对COX介导的PG形成的刺激作用要强得多。从机制上讲,生物类黄酮主要起到减缓COX酶的自杀灭活的作用,但它们似乎并未使灭活的酶重新活化。这项研究的发现表明,某些生物类黄酮可能将作为人类COX酶的天然辅因子。

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