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Ceramide Synthases Are Attractive Drug Targets for Treating Metabolic Diseases
Ceramide synthases (CerS) are central enzymes required for the de-novo synthesis of ceramides and other sphingolipids. They catalyze the addition of different acyl-chains to a sphingoid base, and thus account for much of the rich diversity in the sphingolipid family. Recent studies have demonstrated...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403459/ https://www.ncbi.nlm.nih.gov/pubmed/32849276 http://dx.doi.org/10.3389/fendo.2020.00483 |
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author | Raichur, Suryaprakash |
author_facet | Raichur, Suryaprakash |
author_sort | Raichur, Suryaprakash |
collection | PubMed |
description | Ceramide synthases (CerS) are central enzymes required for the de-novo synthesis of ceramides and other sphingolipids. They catalyze the addition of different acyl-chains to a sphingoid base, and thus account for much of the rich diversity in the sphingolipid family. Recent studies have demonstrated that the acyl-chain is an important determinant of ceramide function, such that a small subset of ceramides (e.g., those containing the C16 or C18 acyl-chain) alter metabolism by inhibiting insulin signaling or inducing mitochondrial fragmentation. Herein I discuss the therapeutic potential of targeting certain ceramide synthase isoforms for the treatment of obesity, insulin resistance, steatohepatitis, and other metabolic disorders. |
format | Online Article Text |
id | pubmed-7403459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74034592020-08-25 Ceramide Synthases Are Attractive Drug Targets for Treating Metabolic Diseases Raichur, Suryaprakash Front Endocrinol (Lausanne) Endocrinology Ceramide synthases (CerS) are central enzymes required for the de-novo synthesis of ceramides and other sphingolipids. They catalyze the addition of different acyl-chains to a sphingoid base, and thus account for much of the rich diversity in the sphingolipid family. Recent studies have demonstrated that the acyl-chain is an important determinant of ceramide function, such that a small subset of ceramides (e.g., those containing the C16 or C18 acyl-chain) alter metabolism by inhibiting insulin signaling or inducing mitochondrial fragmentation. Herein I discuss the therapeutic potential of targeting certain ceramide synthase isoforms for the treatment of obesity, insulin resistance, steatohepatitis, and other metabolic disorders. Frontiers Media S.A. 2020-07-29 /pmc/articles/PMC7403459/ /pubmed/32849276 http://dx.doi.org/10.3389/fendo.2020.00483 Text en Copyright © 2020 Raichur. 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 | Endocrinology Raichur, Suryaprakash Ceramide Synthases Are Attractive Drug Targets for Treating Metabolic Diseases |
title | Ceramide Synthases Are Attractive Drug Targets for Treating Metabolic Diseases |
title_full | Ceramide Synthases Are Attractive Drug Targets for Treating Metabolic Diseases |
title_fullStr | Ceramide Synthases Are Attractive Drug Targets for Treating Metabolic Diseases |
title_full_unstemmed | Ceramide Synthases Are Attractive Drug Targets for Treating Metabolic Diseases |
title_short | Ceramide Synthases Are Attractive Drug Targets for Treating Metabolic Diseases |
title_sort | ceramide synthases are attractive drug targets for treating metabolic diseases |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403459/ https://www.ncbi.nlm.nih.gov/pubmed/32849276 http://dx.doi.org/10.3389/fendo.2020.00483 |
work_keys_str_mv | AT raichursuryaprakash ceramidesynthasesareattractivedrugtargetsfortreatingmetabolicdiseases |