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Aquaglyceroporins: Drug Targets for Metabolic Diseases?

Aquaporins (AQPs) are a family of transmembrane channel proteins facilitating the transport of water, small solutes, and gasses across biological membranes. AQPs are expressed in all tissues and ensure multiple roles under normal and pathophysiological conditions. Aquaglyceroporins are a subfamily o...

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Autores principales: Calamita, Giuseppe, Perret, Jason, Delporte, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048697/
https://www.ncbi.nlm.nih.gov/pubmed/30042691
http://dx.doi.org/10.3389/fphys.2018.00851
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author Calamita, Giuseppe
Perret, Jason
Delporte, Christine
author_facet Calamita, Giuseppe
Perret, Jason
Delporte, Christine
author_sort Calamita, Giuseppe
collection PubMed
description Aquaporins (AQPs) are a family of transmembrane channel proteins facilitating the transport of water, small solutes, and gasses across biological membranes. AQPs are expressed in all tissues and ensure multiple roles under normal and pathophysiological conditions. Aquaglyceroporins are a subfamily of AQPs permeable to glycerol in addition to water and participate thereby to energy metabolism. This review focalizes on the present knowledge of the expression, regulation and physiological roles of AQPs in adipose tissue, liver and endocrine pancreas, that are involved in energy metabolism. In addition, the review aims at summarizing the involvement of AQPs in metabolic disorders, such as obesity, diabetes and liver diseases. Finally, challenges and recent advances related to pharmacological modulation of AQPs expression and function to control and treat metabolic diseases are discussed.
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spelling pubmed-60486972018-07-24 Aquaglyceroporins: Drug Targets for Metabolic Diseases? Calamita, Giuseppe Perret, Jason Delporte, Christine Front Physiol Physiology Aquaporins (AQPs) are a family of transmembrane channel proteins facilitating the transport of water, small solutes, and gasses across biological membranes. AQPs are expressed in all tissues and ensure multiple roles under normal and pathophysiological conditions. Aquaglyceroporins are a subfamily of AQPs permeable to glycerol in addition to water and participate thereby to energy metabolism. This review focalizes on the present knowledge of the expression, regulation and physiological roles of AQPs in adipose tissue, liver and endocrine pancreas, that are involved in energy metabolism. In addition, the review aims at summarizing the involvement of AQPs in metabolic disorders, such as obesity, diabetes and liver diseases. Finally, challenges and recent advances related to pharmacological modulation of AQPs expression and function to control and treat metabolic diseases are discussed. Frontiers Media S.A. 2018-07-10 /pmc/articles/PMC6048697/ /pubmed/30042691 http://dx.doi.org/10.3389/fphys.2018.00851 Text en Copyright © 2018 Calamita, Perret and Delporte. 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(s) 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 Physiology
Calamita, Giuseppe
Perret, Jason
Delporte, Christine
Aquaglyceroporins: Drug Targets for Metabolic Diseases?
title Aquaglyceroporins: Drug Targets for Metabolic Diseases?
title_full Aquaglyceroporins: Drug Targets for Metabolic Diseases?
title_fullStr Aquaglyceroporins: Drug Targets for Metabolic Diseases?
title_full_unstemmed Aquaglyceroporins: Drug Targets for Metabolic Diseases?
title_short Aquaglyceroporins: Drug Targets for Metabolic Diseases?
title_sort aquaglyceroporins: drug targets for metabolic diseases?
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048697/
https://www.ncbi.nlm.nih.gov/pubmed/30042691
http://dx.doi.org/10.3389/fphys.2018.00851
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