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An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes
Diabetes is part of metabolic diseases and is characterized by high blood sugar levels over a prolonged period as result of an insulin-deficient production or an inappropriate response to insulin by our cells. This chronic disease was the direct cause of 1.6 million deaths in 2016 as reported by the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476274/ https://www.ncbi.nlm.nih.gov/pubmed/34589130 http://dx.doi.org/10.1155/2021/3313419 |
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author | Martorell, Miquel Castro, Natalia Victoriano, Montserrat Capó, Xavier Tejada, Silvia Vitalini, Sara Pezzani, Raffaele Sureda, Antoni |
author_facet | Martorell, Miquel Castro, Natalia Victoriano, Montserrat Capó, Xavier Tejada, Silvia Vitalini, Sara Pezzani, Raffaele Sureda, Antoni |
author_sort | Martorell, Miquel |
collection | PubMed |
description | Diabetes is part of metabolic diseases and is characterized by high blood sugar levels over a prolonged period as result of an insulin-deficient production or an inappropriate response to insulin by our cells. This chronic disease was the direct cause of 1.6 million deaths in 2016 as reported by the World Health Organization. Emodin is a natural product and active ingredient of various Chinese herbs with the chemical formula 1,3,8-trihydroxy-6-methylanthraquinone. Diacerein is another naturally occurring anthraquinone (1,8-diacetoxy-3-carboxyanthraquinone) commonly used as commercial drug to treat osteoarthritis. These two anthraquinone derivatives have been shown to exert antidiabetic activities. Emodin seems to enhance the glucose tolerance and insulin sensibility via activation of PPARγ and modulation of metabolic-related genes. Diacerein seems to decrease inflammatory cytokines and increase insulin secretion enhancing insulin sensibility and therefore improving glucose control. Other naturally occurring anthraquinone derivatives, such as catenarin (1,4,6,8-tetrahydroxy-3-methylanthraquinone), have been shown to have antidiabetic activities although few studies have been performed. The synthesis of new emodin derivatives is increasing, but these new molecules have not been tested for diabetes treatment. In the current work, available literature on anthraquinone derivatives' effects in diabetes disease is reviewed. Moreover, we discuss the chemistry, food sources, bioavailability, and toxicity of the naturally occurring anthraquinone with antidiabetic effects. |
format | Online Article Text |
id | pubmed-8476274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-84762742021-09-28 An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes Martorell, Miquel Castro, Natalia Victoriano, Montserrat Capó, Xavier Tejada, Silvia Vitalini, Sara Pezzani, Raffaele Sureda, Antoni Evid Based Complement Alternat Med Review Article Diabetes is part of metabolic diseases and is characterized by high blood sugar levels over a prolonged period as result of an insulin-deficient production or an inappropriate response to insulin by our cells. This chronic disease was the direct cause of 1.6 million deaths in 2016 as reported by the World Health Organization. Emodin is a natural product and active ingredient of various Chinese herbs with the chemical formula 1,3,8-trihydroxy-6-methylanthraquinone. Diacerein is another naturally occurring anthraquinone (1,8-diacetoxy-3-carboxyanthraquinone) commonly used as commercial drug to treat osteoarthritis. These two anthraquinone derivatives have been shown to exert antidiabetic activities. Emodin seems to enhance the glucose tolerance and insulin sensibility via activation of PPARγ and modulation of metabolic-related genes. Diacerein seems to decrease inflammatory cytokines and increase insulin secretion enhancing insulin sensibility and therefore improving glucose control. Other naturally occurring anthraquinone derivatives, such as catenarin (1,4,6,8-tetrahydroxy-3-methylanthraquinone), have been shown to have antidiabetic activities although few studies have been performed. The synthesis of new emodin derivatives is increasing, but these new molecules have not been tested for diabetes treatment. In the current work, available literature on anthraquinone derivatives' effects in diabetes disease is reviewed. Moreover, we discuss the chemistry, food sources, bioavailability, and toxicity of the naturally occurring anthraquinone with antidiabetic effects. Hindawi 2021-09-20 /pmc/articles/PMC8476274/ /pubmed/34589130 http://dx.doi.org/10.1155/2021/3313419 Text en Copyright © 2021 Miquel Martorell et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Martorell, Miquel Castro, Natalia Victoriano, Montserrat Capó, Xavier Tejada, Silvia Vitalini, Sara Pezzani, Raffaele Sureda, Antoni An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes |
title | An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes |
title_full | An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes |
title_fullStr | An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes |
title_full_unstemmed | An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes |
title_short | An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes |
title_sort | update of anthraquinone derivatives emodin, diacerein, and catenarin in diabetes |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476274/ https://www.ncbi.nlm.nih.gov/pubmed/34589130 http://dx.doi.org/10.1155/2021/3313419 |
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