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- Title
Metformin Protects the Intestinal Barrier by Activating Goblet Cell Maturation and Epithelial Proliferation in Radiation-Induced Enteropathy.
- Authors
Jang, Hyosun; Kim, Soyeon; Kim, Hyewon; Oh, Su Hyun; Kwak, Seo Young; Joo, Hyun-Woo; Lee, Seung Bum; Jang, Won Il; Park, Sunhoo; Shim, Sehwan
- Abstract
Radiotherapy or accidental exposure to high-dose radiation can cause severe damage to healthy organs. The gastrointestinal (GI) tract is a radiation-sensitive organ of the body. The intestinal barrier is the first line of defense in the GI tract, and consists of mucus secreted by goblet cells and a monolayer of epithelium. Intestinal stem cells (ISCs) help in barrier maintenance and intestinal function after injury by regulating efficient regeneration of the epithelium. The Wnt/β-catenin pathway plays a critical role in maintaining the intestinal epithelium and regulates ISC self-renewal. Metformin is the most widely used antidiabetic drug in clinical practice, and its anti-inflammatory, antioxidative, and antiapoptotic effects have also been widely studied. In this study, we investigated whether metformin alleviated radiation-induced enteropathy by focusing on its role in protecting the epithelial barrier. We found that metformin alleviated radiation-induced enteropathy, with increased villi length and crypt numbers, and restored the intestinal barrier function in the irradiated intestine. In a radiation-induced enteropathy mouse model, metformin treatment increased tight-junction expression in the epithelium and inhibited bacterial translocation to mesenteric lymph nodes. Metformin increased the number of ISCs from radiation toxicity and enhanced epithelial repair by activating Wnt/β-catenin signaling. These data suggested that metformin may be a potential therapeutic agent for radiation-induced enteropathy.
- Subjects
INTESTINAL diseases; WNT signal transduction; METFORMIN; GASTROINTESTINAL system; INTESTINES; TIGHT junctions; EPITHELIAL cells; EPITHELIUM
- Publication
International Journal of Molecular Sciences, 2022, Vol 23, Issue 11, p5929
- ISSN
1661-6596
- Publication type
Article
- DOI
10.3390/ijms23115929