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PMID: 15852457 Published · ppublish English Journal Article Review

Structure and function studies of glucagon-like peptide-1 (GLP-1): the designing of a novel pharmacological agent for the treatment of diabetes.

Diabetes/metabolism research and reviews ·Vol. 21 ·No. 4 ·2005-00-00 ·Pages 313-31

Hui H, Zhao X, Perfetti R

Abstract

Glucagon-like peptide-1 (GLP-1) is a proglucagon-derived peptide secreted from gut endocrine cells in response to nutrient ingestion. The multifaceted actions of GLP-1 include the following: (1) the stimulation of insulin secretion and of its gene expression, (2) the inhibition of glucagon secretion, (3) the inhibition of food intake, (4) the proliferation and differentiation of beta cells, and (5) the protection of beta-cells from apoptosis. The therapeutic utility of the native GLP-1 molecule is limited by its rapid enzymatic degradation by a serine protease termed dipeptidyl peptidase-IV (DPP-IV). The present article reviews the research studies aimed at elucidating the biosynthesis, metabolism, and molecular characteristics of GLP-1 since it is from these studies that the development of a GLP-1-like pharmacological agent may be derived.

MeSH Terms
Amino Acid Sequence Animals Diabetes Mellitus/drug therapy Drug Design Exons Genome, Human Glucagon/biosynthesis,blood,genetics,metabolism Glucagon-Like Peptide 1 Humans Models, Molecular Molecular Sequence Data Peptide Fragments/biosynthesis,blood,genetics,metabolism Protein Conformation Protein Precursors/biosynthesis,blood,genetics,metabolism
Chemicals
Peptide Fragments Protein Precursors Glucagon-Like Peptide 1 Glucagon
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hui Hongxiang
Division of Endocrinology and Metabolism, Cedars-Sinai Medical Center, Los Angeles, California 90048, USA.
Zhao Xiaoning
Perfetti Riccardo
Article Info
Journal
Diabetes/metabolism research and reviews
Abbr.
Diabetes Metab Res Rev
ISSN
1520-7552
Published
2005-00-00
Pages
313-31
Language
English
Region
England
NLM ID
100883450
Subset
IM
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