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Limonin ameliorates ulcerative colitis by regulating STAT3/miR-214 signaling pathway
- Source :
- International Immunopharmacology. 75:105768
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
Abstract
- Ulcerative colitis (UC) is a major inflammatory bowel disease (IBD) which has become a global public health problem. Limonin is a triterpenoid extracted from citrus which possesses the capacities to against inflammations and cell apoptosis. However, the efficacy and the underlying mechanisms of limonin in the treatment of UC remain unclear. In this study, we first investigated the therapeutic effects of limonin on dextran sodiumsulfate (DSS)-induced UC in vivo by examining the changes of disease activity index (DAI), the colon length, the colon histology, and cyto/chemokine levels. We found that limonin markedly reduced DAI, intestinal damages, and the levels of pro-inflammatory cytokines, such as TNF-α and IL-6. In vitro, limonin significantly repressed the productions of pro-inflammatory cytokines in cultured normal colonic epithelial cells. Mechanistically, we demonstrated that limonin improved the prognosis of UC mainly through downregulating p-STAT3/miR-214 levels. Collectively, our results suggested that limonin was a novel therapeutic agent and it was expected to be translated into the clinic to improve the prognosis of UC.
- Subjects :
- Limonins
Male
STAT3 Transcription Factor
0301 basic medicine
Chemokine
Cell Survival
Colon
Limonin
Immunology
Anti-Inflammatory Agents
Inflammatory bowel disease
Cell Line
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
In vivo
medicine
Animals
Immunology and Allergy
miR-214
STAT3
Pharmacology
biology
Interleukin-6
business.industry
Dextran Sulfate
Epithelial Cells
medicine.disease
Ulcerative colitis
Interleukin-10
Mice, Inbred C57BL
MicroRNAs
030104 developmental biology
chemistry
Apoptosis
030220 oncology & carcinogenesis
Cancer research
biology.protein
Colitis, Ulcerative
business
Signal Transduction
Subjects
Details
- ISSN :
- 15675769
- Volume :
- 75
- Database :
- OpenAIRE
- Journal :
- International Immunopharmacology
- Accession number :
- edsair.doi.dedup.....9a0197029315c3759eca8b0d92f16f2d
- Full Text :
- https://doi.org/10.1016/j.intimp.2019.105768