Flavonoids and Organic Acids Affect Phase II Metabolism based on the Regulation of UGT1A1 Expression and Function.

Lin Zhang, Xuerong Zhang, Caiyan Wang
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Abstract

Background: Exogenous substances modulate metabolism by regulating the expression and function of UDP-glycosyltransferases (UGTs). However, the exact mechanism in the intestine was rarely understood. Herein, we explored the effects of representative flavonoids and organic acids on the regulation of UGT1A1.

Methods: MTT assays and western blot analysis were used to explore the effect of polyphenols. X-ray diffraction was used to reveal the catalytic mechanisms of UGTs.

Results: MTT assays showed that these compounds basically had no cytotoxicity, even in concentrations up to 200 μM. Then, through western blot assays, UGT1A1 expression was increased after being treated with liquiritigenin and caffeic acid. Furthermore, liquiritigenin and caffeic acid enhanced the nuclear translocation of Nrf2. Moreover, a 2.5-Å crystal structure of the complex containing UGTs C-terminal domain and organic acid was solved, and the UDPGA binding pocket could be occupied by organic acid, suggesting the enzyme activity might be impaired by organic acid.

Conclusion: Above all, liquiritigenin and caffeic acid maintained the metabolism balance by upregulating the expression of UGT1A1 via Nrf2 activation and inhibiting the enzyme activity in Caco-2 cells.

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黄酮类化合物和有机酸通过调节 UGT1A1 的表达和功能影响第二阶段代谢
背景:外源性物质通过调节 UDP-糖基转移酶(UGTs)的表达和功能来调节新陈代谢。然而,人们很少了解其在肠道中的确切机制。在此,我们探讨了代表性黄酮类化合物和有机酸对 UGT1A1 的调控作用:方法:采用 MTT 试验和 Western 印迹分析来探讨多酚的影响。采用 X 射线衍射法揭示 UGTs 的催化机理:MTT 试验表明,这些化合物基本上没有细胞毒性,即使浓度高达 200 μM。然后,通过 Western 印迹检测,发现 UGT1A1 的表达在枸杞苷元和咖啡酸处理后有所增加。此外,枸杞苷元和咖啡酸还增强了 Nrf2 的核转位。此外,还解析了含有 UGTs C 端结构域和有机酸的复合物的 2.5 Å 晶体结构,UDPGA 结合袋可能被有机酸占据,表明有机酸可能会损害酶的活性:结论:Liquiritigenin和咖啡酸通过激活Nrf2上调UGT1A1的表达,抑制Caco-2细胞中UGT1A1的活性,从而维持代谢平衡。
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