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Published on: November 18, 2022
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Vaccarin enhances intestinal barrier function in type 2 diabetic mice
Jiang-Nan Sun1, Xiao-Yi Yu1, Bao Hou1
1Wuxi Medical School, Jiangnan University, Wuxi, 214122, Jiangsu Province, PR China.
European Journal of Pharmacology
|July 25, 2021
Summary
Vaccarin, a component of traditional Chinese medicine, improves intestinal barrier function in type 2 diabetes (T2DM) by modulating gut microbiota and inhibiting the ERK/MLCK pathway. This suggests potential therapeutic benefits for T2DM-related gut issues.
Area of Science:
- Gastroenterology and Endocrinology
- Pharmacology and Traditional Medicine
- Molecular Biology
Background:
- Type 2 diabetes (T2DM) is characterized by hyperglycemia and insulin resistance, leading to intestinal barrier dysfunction.
- Vaccarin, derived from Vaccaria, shows promise in managing T2DM in preclinical models.
- Understanding vaccarin's impact on the gut barrier is crucial for T2DM management.
Purpose of the Study:
- To investigate the efficacy of vaccarin in enhancing intestinal barrier function in a T2DM mouse model.
- To elucidate the mechanisms underlying vaccarin's effects on the gut barrier and microbiota.
Main Methods:
- Establishment of a T2DM mouse model using streptozotocin and a high-fat diet.
- Administration of vaccarin (1 mg/kg/day) and assessment of gut microbiota via 16S rRNA sequencing.
- Evaluation of intestinal barrier function using Western blot, qPCR, and morphological analysis; in vitro studies on human intestinal epithelial cells.
Main Results:
- Vaccarin significantly reduced inflammatory mediators in serum and intestinal tissues (P < 0.05).
- Improvements in tight junctions and gut microbiota composition were observed (P < 0.05).
- Vaccarin inhibited the ERK/MLCK signaling pathway, similar to ERK inhibitors, thereby protecting tight junction barriers.
Conclusions:
- Vaccarin protects the intestinal barrier in T2DM by inhibiting the ERK/MLCK pathway and modulating gut microbiota.
- These findings indicate that vaccarin is a potential therapeutic candidate for T2DM-associated intestinal barrier dysfunction.
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