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Bakuchiol mitigates colitis through GPR120 activation
Fangfang Xu1, Jixia Wang2, Tianyu Zhang3
1Jiangxi Provincial Key Laboratory for Pharmacodynamic Material Basis of Traditional Chinese Medicine, Ganjiang Chinese Medicine Innovation Center, Nanchang 330000, China.
Sishen Wan contains bakuchiol, which effectively treats inflammatory bowel disease (IBD) by activating the GPR120 receptor. This study identifies bakuchiol as a promising novel therapeutic agent for IBD.
Area of Science:
- Pharmacology
- Gastroenterology
- Traditional Chinese Medicine
Background:
- Sishen Wan (SSW) is a traditional Chinese herbal formula used for inflammatory bowel disease (IBD).
- The specific active compounds and mechanisms of SSW in treating IBD remain largely unknown.
- This study aimed to elucidate the key components and action mechanisms of SSW.
Purpose of the Study:
- Identify the primary active compound in Sishen Wan (SSW).
- Evaluate the therapeutic efficacy of the identified compound in an inflammatory bowel disease (IBD) model.
- Explore the molecular targets and mechanisms underlying its anti-inflammatory effects.
Main Methods:
- Ultra-high-performance liquid chromatography coupled with mass spectrometry (UHPLC-MS/MS) for chemical analysis.
- Dextran sodium sulfate (DSS)-induced colitis mouse model to assess therapeutic effects.
- Virtual screening, pharmacological assays, RNA sequencing (RNA-seq), and cell-based assays to determine molecular targets and mechanisms.
Main Results:
- Bakuchiol was identified as the main active component of SSW.
- Bakuchiol demonstrated significant therapeutic effects in DSS-induced colitis, comparable or superior to mesalazine.
- Bakuchiol acts as a GPR120 agonist, suppressing inflammatory pathways and partially maintaining epithelial barrier function.
Conclusions:
- Bakuchiol is a key active compound in Sishen Wan (SSW).
- Bakuchiol exerts therapeutic effects in IBD by activating the GPR120 receptor.
- Bakuchiol shows potential as a novel therapeutic agent for inflammatory bowel disease (IBD).
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