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New concept of the glucagon‐like peptide‐1 signaling pathway on pancreatic insulin secretion

The intracellular glucagon‐like peptide‐1 (GLP‐1) signaling pathway, which involves cyclic adenosine monophosphate (cAMP), exchange protein directly activated by cAMP, cAMP‐dependent protein kinase A (PKA) and adenosine triphosphate‐sensitive potassium channels, has been widely accepted as a common...

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Detalles Bibliográficos
Autor principal: Kaku, Kohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078078/
https://www.ncbi.nlm.nih.gov/pubmed/31472102
http://dx.doi.org/10.1111/jdi.13136
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author Kaku, Kohei
author_facet Kaku, Kohei
author_sort Kaku, Kohei
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description The intracellular glucagon‐like peptide‐1 (GLP‐1) signaling pathway, which involves cyclic adenosine monophosphate (cAMP), exchange protein directly activated by cAMP, cAMP‐dependent protein kinase A (PKA) and adenosine triphosphate‐sensitive potassium channels, has been widely accepted as a common mechanism of GLP‐1‐stimulated insulin secretion. Recent studies showed that a stimulatory effect of GLP‐1 is also mediated by cAMP/PKA‐independent mechanisms, including induction of Gαq activity followed by phospholipase C and protein kinase C activation. Furthermore, transient receptor potential 4 and transient receptor potential 5 channels play a role in protein kinase C‐induced Ca(2+) current. This pathway is a unique action mechanism of GLP‐1 at physiologically low concentrations.[Image: see text]
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spelling pubmed-70780782020-03-19 New concept of the glucagon‐like peptide‐1 signaling pathway on pancreatic insulin secretion Kaku, Kohei J Diabetes Investig Editorial The intracellular glucagon‐like peptide‐1 (GLP‐1) signaling pathway, which involves cyclic adenosine monophosphate (cAMP), exchange protein directly activated by cAMP, cAMP‐dependent protein kinase A (PKA) and adenosine triphosphate‐sensitive potassium channels, has been widely accepted as a common mechanism of GLP‐1‐stimulated insulin secretion. Recent studies showed that a stimulatory effect of GLP‐1 is also mediated by cAMP/PKA‐independent mechanisms, including induction of Gαq activity followed by phospholipase C and protein kinase C activation. Furthermore, transient receptor potential 4 and transient receptor potential 5 channels play a role in protein kinase C‐induced Ca(2+) current. This pathway is a unique action mechanism of GLP‐1 at physiologically low concentrations.[Image: see text] John Wiley and Sons Inc. 2019-09-25 2020-03 /pmc/articles/PMC7078078/ /pubmed/31472102 http://dx.doi.org/10.1111/jdi.13136 Text en © 2019 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Editorial
Kaku, Kohei
New concept of the glucagon‐like peptide‐1 signaling pathway on pancreatic insulin secretion
title New concept of the glucagon‐like peptide‐1 signaling pathway on pancreatic insulin secretion
title_full New concept of the glucagon‐like peptide‐1 signaling pathway on pancreatic insulin secretion
title_fullStr New concept of the glucagon‐like peptide‐1 signaling pathway on pancreatic insulin secretion
title_full_unstemmed New concept of the glucagon‐like peptide‐1 signaling pathway on pancreatic insulin secretion
title_short New concept of the glucagon‐like peptide‐1 signaling pathway on pancreatic insulin secretion
title_sort new concept of the glucagon‐like peptide‐1 signaling pathway on pancreatic insulin secretion
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078078/
https://www.ncbi.nlm.nih.gov/pubmed/31472102
http://dx.doi.org/10.1111/jdi.13136
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