Yamamoto Rie, Yamamoto Yasuko, Imai Shinjiro, Fukutomi Ryuta, Ozawa Yoshio, Abe Masako, Matuo Yushi, Saito Kuniaki
Human Health Sciences, Graduate School of Medicine and Faculty of Medicine, Kyoto University, Kyoto-City, Kyoto, Japan.
Graduate School of Nutrition and Environmental Sciences, University of Shizuoka, Shizuoka-City, Shizuoka, Japan.
PLoS One. 2014 Feb 12;9(2):e88789. doi: 10.1371/journal.pone.0088789. eCollection 2014.
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.
吲哚胺2,3-双加氧酶(IDO)1催化L-色氨酸降解的第一步且是限速步骤,具有重要的免疫调节功能。IDO1的活性在包括肿瘤、自身免疫性疾病和各类炎症在内的多种炎症性疾病中会升高。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;检测了16种植物提取物和14种植物化学物质。结果,作为传统日本食品的茗荷花芽甲醇提取物以及源自茗荷花的半日花烷型二萜加拉醛显著抑制了IDO1活性。Lineweaver-Burk图分析表明加拉醛是一种竞争性抑制剂。在使用重组人IDO1的检测系统中,加拉醛使L-犬尿氨酸生成减少,IC₅₀值为7.7 µM,在基于细胞的检测中IC₅₀值为45 nM。此外,机制分析显示加拉醛干扰了核因子-κB的转录功能和干扰素-γ信号通路。加拉醛的这些作用对免疫反应很重要。由于加拉醛对IDO1活性的抑制作用强于色氨酸类似物1-甲基色氨酸,加拉醛作为治疗各种免疫相关疾病的新型药物可能具有巨大潜力。