Glucagon-like peptide 1 and glucose-dependent insulinotropic polypeptide: new advances

Meena Asmar, Jens Juul Holst

46 Citationer (Scopus)

Abstract

PURPOSE OF REVIEW: This article highlights recent advances in our understanding of glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) physiology and their various sites of action beyond the incretin effect. RECENT FINDINGS: Both GLP-1 and GIP stimulate insulin secretion in a glucose-dependent manner and are thus classified as incretins. Beyond glucose-dependent insulin secretion, the peptides have common actions on islet β cells, leading β-cell proliferation and resistance to apoptosis. However, the action of GLP-1 and GIP is not limited to the islet cells; they have regulatory functions in many organs. Recent evidence has suggested that GLP-1 has important beneficial effects in the cardiovascular system and central nervous system. GIP may play a role in promoting energy storage in humans, enhances bone formation via stimulation of osteoblast proliferation and inhibition of apoptosis and may play a role in central nervous system function. SUMMARY: These new findings suggest further application of these hormones for the treatment of conditions such as cardiovascular disease and obesity.

OriginalsprogEngelsk
TidsskriftCurrent Opinion in Endocrinology, Diabetes and Obesity
Vol/bind17
Udgave nummer1
Sider (fra-til)57-62
Antal sider6
ISSN1752-296X
StatusUdgivet - 1 feb. 2010

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