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Pancreatic Aquaporin-7: A Novel Target for Anti-diabetic Drugs?

Aquaporins comprise a family of 13 members of water channels (AQP0-12) that facilitate a rapid transport of water across cell membranes. In some cases, these pores are also permeated by small solutes, particularly glycerol, urea or nitric oxide, among other solutes. Several aquaporins have been iden...

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Autores principales: Méndez-Giménez, Leire, Ezquerro, Silvia, da Silva, Inês V., Soveral, Graça, Frühbeck, Gema, Rodríguez, Amaia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895657/
https://www.ncbi.nlm.nih.gov/pubmed/29675407
http://dx.doi.org/10.3389/fchem.2018.00099
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author Méndez-Giménez, Leire
Ezquerro, Silvia
da Silva, Inês V.
Soveral, Graça
Frühbeck, Gema
Rodríguez, Amaia
author_facet Méndez-Giménez, Leire
Ezquerro, Silvia
da Silva, Inês V.
Soveral, Graça
Frühbeck, Gema
Rodríguez, Amaia
author_sort Méndez-Giménez, Leire
collection PubMed
description Aquaporins comprise a family of 13 members of water channels (AQP0-12) that facilitate a rapid transport of water across cell membranes. In some cases, these pores are also permeated by small solutes, particularly glycerol, urea or nitric oxide, among other solutes. Several aquaporins have been identified in the pancreas, an exocrine and endocrine organ that plays an essential role in the onset of insulin resistance and type 2 diabetes. The exocrine pancreas, which accounts for 90% of the total pancreas, secretes daily large volumes of a near-isotonic fluid containing digestive enzymes into the duodenum. AQP1, AQP5, and AQP8 contribute to fluid secretion especially from ductal cells, whereas AQP12 allows the proper maturation and exocytosis of secretory granules in acinar cells of the exocrine pancreas. The endocrine pancreas (10% of the total pancreatic cells) is composed by the islets of Langerhans, which are distributed in α, β, δ, ε, and pancreatic polypeptide (PP) cells that secrete glucagon, insulin, somatostatin, ghrelin and PP, respectively. AQP7, an aquaglyceroporin permeated by water and glycerol, is expressed in pancreatic β-cells and murine studies have confirmed its participation in insulin secretion, triacylglycerol synthesis and proliferation of these endocrine cells. In this regard, transgenic AQP7-knockout mice develop adult-onset obesity, hyperinsulinemia, increased intracellular triacylglycerol content and reduced β-cell mass in Langerhans islets. Moreover, we have recently reported that AQP7 upregulation in β-cells after bariatric surgery, an effective weight loss surgical procedure, contributes, in part, to the improvement of pancreatic steatosis and insulin secretion through the increase of intracytoplasmic glycerol in obese rats. Human studies remain scarce and controversial, with some rare cases of loss-of function mutations of the AQP7 gene being associated with the onset of type 2 diabetes. The present Review is focused on the role of aquaporins in the physiology and pathophysiology of the pancreas, highlighting the role of pancreatic AQP7 as a novel player in the control of β-cell function and a potential anti-diabetic-drug.
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spelling pubmed-58956572018-04-19 Pancreatic Aquaporin-7: A Novel Target for Anti-diabetic Drugs? Méndez-Giménez, Leire Ezquerro, Silvia da Silva, Inês V. Soveral, Graça Frühbeck, Gema Rodríguez, Amaia Front Chem Chemistry Aquaporins comprise a family of 13 members of water channels (AQP0-12) that facilitate a rapid transport of water across cell membranes. In some cases, these pores are also permeated by small solutes, particularly glycerol, urea or nitric oxide, among other solutes. Several aquaporins have been identified in the pancreas, an exocrine and endocrine organ that plays an essential role in the onset of insulin resistance and type 2 diabetes. The exocrine pancreas, which accounts for 90% of the total pancreas, secretes daily large volumes of a near-isotonic fluid containing digestive enzymes into the duodenum. AQP1, AQP5, and AQP8 contribute to fluid secretion especially from ductal cells, whereas AQP12 allows the proper maturation and exocytosis of secretory granules in acinar cells of the exocrine pancreas. The endocrine pancreas (10% of the total pancreatic cells) is composed by the islets of Langerhans, which are distributed in α, β, δ, ε, and pancreatic polypeptide (PP) cells that secrete glucagon, insulin, somatostatin, ghrelin and PP, respectively. AQP7, an aquaglyceroporin permeated by water and glycerol, is expressed in pancreatic β-cells and murine studies have confirmed its participation in insulin secretion, triacylglycerol synthesis and proliferation of these endocrine cells. In this regard, transgenic AQP7-knockout mice develop adult-onset obesity, hyperinsulinemia, increased intracellular triacylglycerol content and reduced β-cell mass in Langerhans islets. Moreover, we have recently reported that AQP7 upregulation in β-cells after bariatric surgery, an effective weight loss surgical procedure, contributes, in part, to the improvement of pancreatic steatosis and insulin secretion through the increase of intracytoplasmic glycerol in obese rats. Human studies remain scarce and controversial, with some rare cases of loss-of function mutations of the AQP7 gene being associated with the onset of type 2 diabetes. The present Review is focused on the role of aquaporins in the physiology and pathophysiology of the pancreas, highlighting the role of pancreatic AQP7 as a novel player in the control of β-cell function and a potential anti-diabetic-drug. Frontiers Media S.A. 2018-04-05 /pmc/articles/PMC5895657/ /pubmed/29675407 http://dx.doi.org/10.3389/fchem.2018.00099 Text en Copyright © 2018 Méndez-Giménez, Ezquerro, da Silva, Soveral, Frühbeck and Rodríguez. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Méndez-Giménez, Leire
Ezquerro, Silvia
da Silva, Inês V.
Soveral, Graça
Frühbeck, Gema
Rodríguez, Amaia
Pancreatic Aquaporin-7: A Novel Target for Anti-diabetic Drugs?
title Pancreatic Aquaporin-7: A Novel Target for Anti-diabetic Drugs?
title_full Pancreatic Aquaporin-7: A Novel Target for Anti-diabetic Drugs?
title_fullStr Pancreatic Aquaporin-7: A Novel Target for Anti-diabetic Drugs?
title_full_unstemmed Pancreatic Aquaporin-7: A Novel Target for Anti-diabetic Drugs?
title_short Pancreatic Aquaporin-7: A Novel Target for Anti-diabetic Drugs?
title_sort pancreatic aquaporin-7: a novel target for anti-diabetic drugs?
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895657/
https://www.ncbi.nlm.nih.gov/pubmed/29675407
http://dx.doi.org/10.3389/fchem.2018.00099
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