Review article: a comparison of glucagon‐like peptides 1 and 2. Issue 1 (5th November 2012)
- Record Type:
- Journal Article
- Title:
- Review article: a comparison of glucagon‐like peptides 1 and 2. Issue 1 (5th November 2012)
- Main Title:
- Review article: a comparison of glucagon‐like peptides 1 and 2
- Authors:
- Janssen, P.
Rotondo, A.
Mulé, F.
Tack, J. - Abstract:
- <abstract abstract-type="main" id="apt12092-abs-0001"> <title>Summary</title> <sec id="apt12092-sec-0001" sec-type="section"> <title>Background</title> <p>Recent advancements in understanding the roles and functions of glucagon‐like peptide 1 (GLP‐1) and 2 (GLP‐2) have provided a basis for targeting these peptides in therapeutic strategies.</p> </sec> <sec id="apt12092-sec-0002" sec-type="section"> <title>Aim</title> <p>To summarise the preclinical and clinical research supporting the discovery of new therapeutic molecules targeting GLP‐1 and GLP‐2.</p> </sec> <sec id="apt12092-sec-0003" sec-type="section"> <title>Methods</title> <p>This review is based on a comprehensive PubMed search, representing literature published during the past 30 years related to GLP‐1 and GLP‐2.</p> </sec> <sec id="apt12092-sec-0004" sec-type="section"> <title>Results</title> <p>Although produced and secreted together primarily from L cells of the intestine in response to ingestion of nutrients, GLP‐1 and GLP‐2 exhibit distinctive biological functions that are governed by the expression of their respective receptors, GLP‐1R and GLP‐2R. Through widespread expression in the pancreas, intestine, nervous tissue, et cetera, GLP‐1Rs facilitates an incretin effect along with effects on appetite and satiety. GLP‐1 analogues resistant to degradation by dipeptidyl peptidase‐IV and inhibitors of dipeptidyl peptidase‐IV have been developed to aid treatment of diabetes and obesity. The GLP‐2R is expressed<abstract abstract-type="main" id="apt12092-abs-0001"> <title>Summary</title> <sec id="apt12092-sec-0001" sec-type="section"> <title>Background</title> <p>Recent advancements in understanding the roles and functions of glucagon‐like peptide 1 (GLP‐1) and 2 (GLP‐2) have provided a basis for targeting these peptides in therapeutic strategies.</p> </sec> <sec id="apt12092-sec-0002" sec-type="section"> <title>Aim</title> <p>To summarise the preclinical and clinical research supporting the discovery of new therapeutic molecules targeting GLP‐1 and GLP‐2.</p> </sec> <sec id="apt12092-sec-0003" sec-type="section"> <title>Methods</title> <p>This review is based on a comprehensive PubMed search, representing literature published during the past 30 years related to GLP‐1 and GLP‐2.</p> </sec> <sec id="apt12092-sec-0004" sec-type="section"> <title>Results</title> <p>Although produced and secreted together primarily from L cells of the intestine in response to ingestion of nutrients, GLP‐1 and GLP‐2 exhibit distinctive biological functions that are governed by the expression of their respective receptors, GLP‐1R and GLP‐2R. Through widespread expression in the pancreas, intestine, nervous tissue, et cetera, GLP‐1Rs facilitates an incretin effect along with effects on appetite and satiety. GLP‐1 analogues resistant to degradation by dipeptidyl peptidase‐IV and inhibitors of dipeptidyl peptidase‐IV have been developed to aid treatment of diabetes and obesity. The GLP‐2R is expressed almost exclusively in the stomach and bowel. The most apparent role for GLP‐2 is its promotion of growth and function of intestinal mucosa, which has been targeted for therapies that promote repair and adaptive growth. These are used as treatments for intestinal failure and related conditions.</p> </sec> <sec id="apt12092-sec-0005" sec-type="section"> <title>Conclusions</title> <p>Our growing understanding of the biology and function of GLP‐1, GLP‐2 and corresponding receptors has fostered further discovery of fundamental biological function as well as new categories of potent therapeutic medicines.</p> </sec> </abstract> … (more)
- Is Part Of:
- Alimentary pharmacology & therapeutics. Volume 37:Issue 1(2013)
- Journal:
- Alimentary pharmacology & therapeutics
- Issue:
- Volume 37:Issue 1(2013)
- Issue Display:
- Volume 37, Issue 1 (2013)
- Year:
- 2013
- Volume:
- 37
- Issue:
- 1
- Issue Sort Value:
- 2013-0037-0001-0000
- Page Start:
- 18
- Page End:
- 36
- Publication Date:
- 2012-11-05
- Subjects:
- Digestive organs -- Diseases -- Treatment -- Periodicals
Digestive organs -- Effect of drugs on -- Periodicals
Gastrointestinal system -- Diseases -- Treatment -- Periodicals
Gastrointestinal system -- Effect of drugs on -- Periodicals
615.73 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2036 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/apt.12092 ↗
- Languages:
- English
- ISSNs:
- 0269-2813
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0787.886000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3055.xml