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Effects of Various Phytochemicals on Indoleamine 2,3-Dioxygenase 1 Activity: Galanal Is a Novel, Competitive Inhibitor of the Enzyme

机译:各种植物化学物质对吲哚胺2,3-双加氧酶1活性的影响:加拉纳尔是一种新型的竞争性酶抑制剂。

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摘要

Indoleamine 2,3-dioxygenase (IDO) 1, that catalyzes the first and rate-limiting step in the degradation of L-tryptophan, has an important immunomodulatory function. The activity of IDO1 increases in various inflammatory diseases, including tumors, autoimmune diseases, and different kinds of inflammation. We evaluated the suppressive effect of plant extracts or phytochemicals on IDO1 induction and activity; sixteen kinds of plants extracts and fourteen kinds of phytochemicals were examined. As a result, the methanol extracts of Myoga flower buds, which are traditional Japanese foods, and labdane-type diterpene galanal derived from Myoga flowers significantly suppressed IDO1 activity. The Lineweaver-Burk plot analysis indicated that galanal is a competitive inhibitor. Galanal attenuated L-kynurenine formation with an IC50 value of 7.7 µM in the assay system using recombinant human IDO1, and an IC50 value of 45 nM in the cell-based assay. Further, mechanistic analysis revealed that galanal interfered with the transcriptional function of the nuclear factor-κB and the interferon-γ signaling pathway. These effects of galanal are important for immune response. Because the inhibitory effect of galanal on IDO1 activity was stronger than that of 1-methyl tryptophan, a tryptophan analog, galanal may have great potential as the novel drug for various immune-related diseases.
机译:催化L-色氨酸降解的第一步和限速步骤的吲哚胺2,3-双加氧酶(IDO)1具有重要的免疫调节功能。 IDO1的活性在各种炎症性疾病(包括肿瘤,自身免疫性疾病和各种炎症)中都增加。我们评估了植物提取物或植物化学物质对IDO1诱导和活性的抑制作用。检查了16种植物提取物和14种植物化学物质。结果,作为日本传统食品的Myoga花蕾的甲醇提取物和Myoga花衍生的拉丹烷型二萜丙二醛可显着抑制IDO1活性。 Lineweaver-Burk图分析表明,丙二醛是竞争性抑制剂。在使用重组人IDO1的测定系统中,Galanal减弱了L-犬尿氨酸的形成,IC50值为7.7 µM,在基于细胞的测定中,IC50值为45 nM。进一步的机理分析表明,加拉纳尔干扰了核因子-κB和干扰素-γ信号通路的转录功能。丙二醛的这些作用对于免疫应答是重要的。由于甘丙醛对IDO1活性的抑制作用强于色氨酸类似物1-甲基色氨酸,因此甘丙醛作为治疗多种免疫相关疾病的新药具有巨大潜力。

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