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
- ulcerative colitis
- insulin resistance
- toll like receptor
- binding protein
- rheumatoid arthritis
- type diabetes
- physical activity
- adipose tissue
- transcription factor
- diabetic rats
- mass spectrometry
- molecular dynamics
- skeletal muscle
- molecular dynamics simulations
- bone marrow
- pi k akt
- high glucose
- helicobacter pylori infection
- inflammatory response
- high resolution
- data analysis
- combination therapy
- dna binding
- cell therapy
- protein protein
- atomic force microscopy
- replacement therapy
- anti inflammatory