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Cited 186 time in webofscience Cited 203 time in scopus
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Anti-diabetic actions of glucagon-like peptide-1 on pancreatic beta-cells

Authors
Lee, Young-SunJun, Hee-Sook
Issue Date
Jan-2014
Publisher
W B SAUNDERS CO-ELSEVIER INC
Keywords
Pancreatic islet; Incretin hormone; Type 2 diabetes; Proliferation; Anti-apoptosis
Citation
METABOLISM-CLINICAL AND EXPERIMENTAL, v.63, no.1, pp.9 - 19
Journal Title
METABOLISM-CLINICAL AND EXPERIMENTAL
Volume
63
Number
1
Start Page
9
End Page
19
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12952
DOI
10.1016/j.metabol.2013.09.010
ISSN
0026-0495
Abstract
Glucagon-like peptide-1 (GLP-1), an incretin hormone, is released from intestinal L-cells in response to nutrients. GLP-1 lowers blood glucose levels by stimulating insulin secretion from pancreatic beta-cells in a glucose-dependent manner. In addition, GLP-1 slows gastric emptying, suppresses appetite, reduces plasma glucagon, and stimulates glucose disposal, which are beneficial for glucose homeostasis. Therefore, incretin-based therapies such as GLP-1 receptor agonists and inhibitors of dipeptidyl peptidase IV, an enzyme which inactivates GLP-1, have been developed for treatment of diabetes. This review outlines our knowledge of the actions of GLP-1 on insulin secretion and biosynthesis, beta-cell proliferation and regeneration, and protection against beta-cell damage, as well as the involvement of recently discovered signaling pathways of GLP-1 action, mainly focusing on pancreatic beta-cells. (C) 2014 Elsevier Inc. All rights reserved.
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