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The Role of SIRT1 in Diabetic Kidney Disease
Sirtuins (SIRTs) are members of the silent information regulator 2 family. In mammals, of the seven known SIRTs, SIRT1 function is most studied and has been shown to regulate wide range of cellular functions that affect metabolic homeostasis and aging. SIRT1 exerts anti-apoptotic, anti-oxidative, an...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191277/ https://www.ncbi.nlm.nih.gov/pubmed/25346724 http://dx.doi.org/10.3389/fendo.2014.00166 |
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author | Yacoub, Rabi Lee, Kyung He, John Cijiang |
author_facet | Yacoub, Rabi Lee, Kyung He, John Cijiang |
author_sort | Yacoub, Rabi |
collection | PubMed |
description | Sirtuins (SIRTs) are members of the silent information regulator 2 family. In mammals, of the seven known SIRTs, SIRT1 function is most studied and has been shown to regulate wide range of cellular functions that affect metabolic homeostasis and aging. SIRT1 exerts anti-apoptotic, anti-oxidative, and anti-inflammatory effects against cellular injury, and protects the cells through the regulation of mitochondrial biogenesis, autophagy, and metabolism in response to the cellular energy and redox status. SIRT1 also promotes vasodilation and protects vascular tissues. In humans and animal models with diabetic kidney disease (DKD), its expression tends to be decreased in renal cells, and increased expression of SIRT1 was found to play a renal protective role in animal models with DKD. In this review, we discuss the role and potential mechanisms by which SIRT1 protects against DKD. |
format | Online Article Text |
id | pubmed-4191277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41912772014-10-24 The Role of SIRT1 in Diabetic Kidney Disease Yacoub, Rabi Lee, Kyung He, John Cijiang Front Endocrinol (Lausanne) Endocrinology Sirtuins (SIRTs) are members of the silent information regulator 2 family. In mammals, of the seven known SIRTs, SIRT1 function is most studied and has been shown to regulate wide range of cellular functions that affect metabolic homeostasis and aging. SIRT1 exerts anti-apoptotic, anti-oxidative, and anti-inflammatory effects against cellular injury, and protects the cells through the regulation of mitochondrial biogenesis, autophagy, and metabolism in response to the cellular energy and redox status. SIRT1 also promotes vasodilation and protects vascular tissues. In humans and animal models with diabetic kidney disease (DKD), its expression tends to be decreased in renal cells, and increased expression of SIRT1 was found to play a renal protective role in animal models with DKD. In this review, we discuss the role and potential mechanisms by which SIRT1 protects against DKD. Frontiers Media S.A. 2014-10-09 /pmc/articles/PMC4191277/ /pubmed/25346724 http://dx.doi.org/10.3389/fendo.2014.00166 Text en Copyright © 2014 Yacoub, Lee and He. 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) or licensor 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 Yacoub, Rabi Lee, Kyung He, John Cijiang The Role of SIRT1 in Diabetic Kidney Disease |
title | The Role of SIRT1 in Diabetic Kidney Disease |
title_full | The Role of SIRT1 in Diabetic Kidney Disease |
title_fullStr | The Role of SIRT1 in Diabetic Kidney Disease |
title_full_unstemmed | The Role of SIRT1 in Diabetic Kidney Disease |
title_short | The Role of SIRT1 in Diabetic Kidney Disease |
title_sort | role of sirt1 in diabetic kidney disease |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191277/ https://www.ncbi.nlm.nih.gov/pubmed/25346724 http://dx.doi.org/10.3389/fendo.2014.00166 |
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