Naringenin as a natural immunomodulator against T cell-mediated autoimmune diseases: literature review and network-based pharmacology study

被引:21
作者
Liu, Zejin [1 ,2 ]
Niu, Xinli [3 ]
Wang, Junpeng [1 ,2 ]
机构
[1] Henan Univ, Huaihe Hosp, Infect & Immun Inst, Kaifeng, Peoples R China
[2] Henan Univ, Huaihe Hosp, Translat Med Ctr, Kaifeng, Peoples R China
[3] Henan Univ, Sch Life Sci, Kaifeng, Peoples R China
基金
中国国家自然科学基金;
关键词
Flavonoid; naringenin; T cells; autoimmune diseases; network pharmacology; inflammation; NF-KAPPA-B; COLLAGEN-INDUCED ARTHRITIS; MULTIPLE-SCLEROSIS; INFLAMMATORY RESPONSES; FLAVONOID NARINGENIN; ALPHA PRODUCTION; CROHNS-DISEASE; CANCER-CELLS; INHIBITOR; TNF;
D O I
10.1080/10408398.2022.2092054
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
T cells, especially CD4(+) T helper (Th) cells, play a vital role in the pathogenesis of specific autoimmune diseases. Naringenin, a citrus flavonoid, exhibits anti-inflammatory, anti-oxidant, and antitumor properties, which have been verified in animal autoimmune disease models. However, naringenin's possible effects and molecular mechanisms in T cell-mediated autoimmune diseases are unclear. This review summarizes the findings of previous studies and predicts the target of naringenin in T cell-mediated autoimmune disorders such as multiple sclerosis, inflammatory bowel disease, and rheumatoid arthritis through network pharmacology analysis. We performed DAVID enrichment analysis, protein-protein interaction analysis, and molecular docking to predict the positive effect of naringenin on T cell-mediated autoimmune disorders. Sixteen common genes were screened, among which the core genes were PTGS2, ESR1, CAT, CASP3, MAPK1, and AKT1. The possible molecular mechanism relates to HIF-1, estrogen, TNF, and NF-kappa B signaling pathways. Our findings have significance for future naringenin treatment of T cell-mediated autoimmune diseases.
引用
收藏
页码:11026 / 11043
页数:18
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