GLP-1 and Intestinal Diseases

被引:37
|
作者
Hunt, Jenna Elizabeth [1 ]
Holst, Jens Juul [1 ,2 ]
Jeppesen, Palle Bekker [3 ]
Kissow, Hannelouise [1 ,2 ]
机构
[1] Univ Copenhagen, Fac Hlth & Med Sci, Dept Biomed Sci, DK-2200 Copenhagen, Denmark
[2] Univ Copenhagen, Fac Hlth & Med Sci, Novo Nordisk Fdn, Ctr Basic Metab Res, DK-2200 Copenhagen, Denmark
[3] Rigshosp, Dept Med Gastroenterol & Hepatol, DK-2200 Copenhagen, Denmark
关键词
GLP-1; intestinal disease; short-bowel syndrome (SBS); mucositis; inflammatory bowel disease (IBD); coeliac disease; GLUCAGON-LIKE PEPTIDE-1; INFLAMMATORY-BOWEL-DISEASE; RECEPTOR AGONISTS; GLYCEMIC CONTROL; KAPPA-B; PLASMA; CELLS; MECHANISMS; SECRETION; EXENATIDE;
D O I
10.3390/biomedicines9040383
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulating evidence implicates glucagon-like peptide-1 (GLP-1) to have, beyond glucose maintenance, a beneficial role in the gastrointestinal tract. Here, we review emerging data investigating GLP-1 as a novel treatment for intestinal diseases, including inflammatory bowel diseases, short-bowel syndrome, intestinal toxicities and coeliac disease. Possible beneficial mechanisms for these diseases include GLP-1 ' s influence on gastric emptying, its anti-inflammatory properties and its intestinotrophic effect. The current knowledge basis derives from the available GLP-1 agonist treatments in experimental animals and small clinical trials. However, new novel strategies including dual GLP-1/GLP-2 agonists are also in development for the treatment of intestinal diseases.
引用
收藏
页数:14
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