Ferroptosis in the colon epithelial cells as a therapeutic target for ulcerative colitis

被引:18
|
作者
Yokote, Akihito [1 ]
Imazu, Noriyuki [1 ]
Umeno, Junji [1 ]
Kawasaki, Keisuke [1 ]
Fujioka, Shin [2 ]
Fuyuno, Yuta [1 ]
Matsuno, Yuichi [1 ]
Moriyama, Tomohiko [3 ]
Miyawaki, Kohta [4 ]
Akashi, Koichi [4 ]
Kitazono, Takanari [1 ]
Torisu, Takehiro [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Med & Clin Sci, Maidashi 3-1-1,Higashi ku, Fukuoka 8128582, Japan
[2] Kyushu Univ Hosp, Dept Endoscop Diagnost & Therapeut, Fukuoka 8128582, Japan
[3] Kyushu Univ Hosp, Int Med Dept, Fukuoka 8128582, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Dept Med & Biosyst Sci, Fukuoka 8128582, Japan
关键词
Ferroptosis; Indigo naturalis; Ulcerative colitis; Glutathione; NRF2; INDIGO NATURALIS; OXIDATIVE STRESS; CLINICAL-EFFICACY; NRF2; DISEASES; DIFFERENTIATION; ASSOCIATION; ACTIVATION; EXPRESSION; PATHWAY;
D O I
10.1007/s00535-023-02016-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BackgroundFerroptosis, a type of programmed cell death triggered by oxidative stress, was suspected to play a role in ulcerative colitis. Indigo naturalis is highly effective against ulcerative colitis, but its mechanism is unclear. This study found that indigo naturalis treatment suppressed ferroptosis.MethodsWe analyzed 770 mRNA expressions of patients with ulcerative colitis. Suppression of ferroptosis by indigo naturalis treatment was shown using a cell death assay. Malondialdehyde levels and reactive oxygen species were analyzed in CaCo-2 cells treated with indigo naturalis. Glutathione metabolism was shown by metabolomic analysis. Extraction of the ingredients indigo naturalis from the rectal mucosa was performed using liquid chromatograph-mass spectrometry.ResultsGene expression profiling showed that indigo naturalis treatment increased antioxidant genes in the mucosa of patients with ulcerative colitis. In vitro analysis showed that nuclear factor erythroid-2-related factor 2-related antioxidant gene expression was upregulated by indigo naturalis. Indigo naturalis treatment rendered cells resistant to ferroptosis. Metabolomic analysis suggested that an increase in reduced glutathione by indigo naturalis. The protein expression of CYP1A1 and GPX4 was increased in the rectum by treatment with indigo naturalis. The main ingredients of indigo naturalis, indirubin and indigo inhibited ferroptosis. Indirubin was detected in the rectal mucosa of patients with ulcerative colitis who were treated with indigo naturalis.ConclusionsSuppression of ferroptosis by indigo naturalis in the intestinal epithelium could be therapeutic target for ulcerative colitis. The main active ingredient of indigo naturalis may be indirubin.
引用
收藏
页码:868 / 882
页数:15
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