Atractylodin Ameliorates Colitis via PPARα Agonism.
Gwangbeom HeoYuju KimEun-La KimSoyeong ParkSang Hoon RheeJee H JungEunok ImPublished in: International journal of molecular sciences (2023)
Atractylodin is a major compound in the rhizome of Atractylodes lancea , an oriental herbal medicine used for the treatment of gastrointestinal diseases, including dyspepsia, nausea, and diarrhea. Recent studies have shown that atractylodin exerts anti-inflammatory effects in various inflammatory diseases. Herein, we investigated the anti-colitis effects of atractylodin and its molecular targets. We determined the non-cytotoxic concentration of atractylodin (50 μM) using a cell proliferation assay in colonic epithelial cells. We found that pretreatment with atractylodin significantly inhibits tumor necrosis factor-α-induced phosphorylation of nuclear factor-κ-light-chain-enhancer of activated B in HCT116 cells. Through docking simulation analysis, luciferase assays, and in vitro binding assays, we found that atractylodin has an affinity for peroxisome proliferator-activated receptor alpha (PPARα). Daily administration of atractylodin (40 mg/kg) increased the survival rate of mice in a dextran sodium sulfate-induced colitis mouse model. Thus, atractylodin can be a good strategy for colitis therapy through inducing PPARα-dependent pathways.
Keyphrases
- mouse model
- nuclear factor
- cell proliferation
- high throughput
- insulin resistance
- ulcerative colitis
- induced apoptosis
- toll like receptor
- cell cycle arrest
- oxidative stress
- stem cells
- type diabetes
- binding protein
- fatty acid
- transcription factor
- immune response
- mass spectrometry
- small molecule
- molecular dynamics simulations
- signaling pathway
- single molecule
- atomic force microscopy
- combination therapy
- dna binding
- pi k akt
- free survival