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L‐serine: a neglected amino acid with a potential therapeutic role in diabetes

L‐serine is classified as a non‐essential amino acid; however, L‐serine is indispensable having a central role in a broad range of cellular processes. Growing evidence suggests a role for L‐serine in the development of diabetes mellitus and its related complications, with L‐serine being positively c...

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Detalles Bibliográficos
Autores principales: Holm, Laurits J., Buschard, Karsten
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/PMC6851881/
https://www.ncbi.nlm.nih.gov/pubmed/31344283
http://dx.doi.org/10.1111/apm.12987
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author Holm, Laurits J.
Buschard, Karsten
author_facet Holm, Laurits J.
Buschard, Karsten
author_sort Holm, Laurits J.
collection PubMed
description L‐serine is classified as a non‐essential amino acid; however, L‐serine is indispensable having a central role in a broad range of cellular processes. Growing evidence suggests a role for L‐serine in the development of diabetes mellitus and its related complications, with L‐serine being positively correlated to insulin secretion and sensitivity. L‐serine metabolism is altered in type 1, type 2, and gestational diabetes, and L‐serine supplementations improve glucose homeostasis and mitochondrial function, and reduce neuronal death. Additionally, L‐serine lowers the incidence of autoimmune diabetes in NOD mice. Dietary supplementations of L‐serine are generally regarded as safe (GRAS) by the FDA. Therefore, we believe that L‐serine should be considered as an emerging therapeutic option in diabetes, although work remains in order to fully understand the role of L‐serine in diabetes.
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spelling pubmed-68518812019-11-18 L‐serine: a neglected amino acid with a potential therapeutic role in diabetes Holm, Laurits J. Buschard, Karsten APMIS Review Article L‐serine is classified as a non‐essential amino acid; however, L‐serine is indispensable having a central role in a broad range of cellular processes. Growing evidence suggests a role for L‐serine in the development of diabetes mellitus and its related complications, with L‐serine being positively correlated to insulin secretion and sensitivity. L‐serine metabolism is altered in type 1, type 2, and gestational diabetes, and L‐serine supplementations improve glucose homeostasis and mitochondrial function, and reduce neuronal death. Additionally, L‐serine lowers the incidence of autoimmune diabetes in NOD mice. Dietary supplementations of L‐serine are generally regarded as safe (GRAS) by the FDA. Therefore, we believe that L‐serine should be considered as an emerging therapeutic option in diabetes, although work remains in order to fully understand the role of L‐serine in diabetes. John Wiley and Sons Inc. 2019-09-02 2019-10 /pmc/articles/PMC6851881/ /pubmed/31344283 http://dx.doi.org/10.1111/apm.12987 Text en © 2019 The Authors. APMIS published by John Wiley & Sons Ltd on behalf of Scandinavian Societies for Medical Microbiology and Pathology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Holm, Laurits J.
Buschard, Karsten
L‐serine: a neglected amino acid with a potential therapeutic role in diabetes
title L‐serine: a neglected amino acid with a potential therapeutic role in diabetes
title_full L‐serine: a neglected amino acid with a potential therapeutic role in diabetes
title_fullStr L‐serine: a neglected amino acid with a potential therapeutic role in diabetes
title_full_unstemmed L‐serine: a neglected amino acid with a potential therapeutic role in diabetes
title_short L‐serine: a neglected amino acid with a potential therapeutic role in diabetes
title_sort l‐serine: a neglected amino acid with a potential therapeutic role in diabetes
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851881/
https://www.ncbi.nlm.nih.gov/pubmed/31344283
http://dx.doi.org/10.1111/apm.12987
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