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GLP-1 suppresses ga...
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Hellström, P. M.Department of Medicine Karolinska Institutet, Stockholm
(författare)
GLP-1 suppresses gastrointestinal motility and inhibits the migrating motor complex in healthy subjects and patients with irritable bowel syndrome
- Artikel/kapitelEngelska2008
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Wiley,2008
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LIBRIS-ID:oai:DiVA.org:liu-43522
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https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-43522URI
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https://doi.org/10.1111/j.1365-2982.2007.01079.xDOI
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http://kipublications.ki.se/Default.aspx?queryparsed=id:117031750URI
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Språk:engelska
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Sammanfattning på:engelska
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Ämneskategori:art swepub-publicationtype
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Glucagon-like peptide-1 (GLP-1) is released after food intake to act as an incretin. GLP-1 also inhibits gastric emptying and increases satiety. In rats, GLP-1 inhibits small bowel motility. Our aim was to study the effects of GLP-1 on gastrointestinal motility in healthy subjects and patients with irritable bowel syndrome (IBS). Antro-duodeno-jejunal manometry was carried out during a 4-h control period with saline, followed by a 4-h period with intravenous GLP-1 (healthy: 0.7 and 1.2 pmol kg-1 min-1 (n = 16), IBS, 1.2 and 2.5 pmol kg-1 min-1 (n = 14). Plasma was analysed for GLP-1 and gut hormones, and gut tissue expression of GLP-1 receptor was studied. In healthy subjects, GLP-1 0.7 pmol kg-1 min-1 reduced the migrating motor complexes (MMCs) from a median of 2 (range 2-3) to 0.5 (0-2), and motility index from 4.9 ± 0.1 to 4.3 ± 0.3 ln ∑(mmHg*s min-1) in jejunum, while GLP-1 1.2 pmol kg -1 min-1 diminshed MMCs from 2 (2-3) to 1.5 (1-2.5), and motility index from 5.2 ± 0.2 to 4.4 ± 0.2. In IBS patients, GLP-1 1.2 pmol kg-1 min-1 reduced the MMCs from 2.5 (2-3.5) to 1 (0-1.5) without affecting motility index. At 2.5 pmol kg-1 min -1 GLP-1 decreased MMCs from 2 (1.5-3) to 1 (0.5-1.5), and motility index from 5.2 ± 0.2 to 4.0 ± 0.5. Motility responses to GLP-1 were similar in antrum and duodenum. Presence of the GLP-1 receptor in the gut was verified by reverse transcriptase PCR. In conclusion, the gut peptide GLP-1 decreases motility in the antro-duodeno-jejunal region and inhibits the MMC in healthy subjects and IBS patients. © 2008 The Authors.
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Näslund, E.Karolinska Institutet
(författare)
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Edholm, T.Department of Medicine Karolinska Institutet, Stockholm
(författare)
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Schmidt, P. T.Karolinska Institutet
(författare)
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Kristensen, J.Department of Medicine Karolinska Institutet, Stockholm
(författare)
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Theodorsson, Elvar,1953-Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Klinisk kemi(Swepub:liu)elvth65
(författare)
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Holst, J. J.§Department of Medical Physiology University of Copenhagen, Denmark
(författare)
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Efendic, S.Department of Molecular Medicine and Surgery Karolinska Institutet, Stockholm
(författare)
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Karolinska InstitutetDepartment of Medicine Karolinska Institutet, Stockholm
(creator_code:org_t)
Sammanhörande titlar
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Ingår i:Neurogastroenterology and Motility: Wiley20:6, s. 649-6591350-19251365-2982
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