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Oncocalyxone A Functions As an Anti-Glycation Agent In Vitro
Advanced glycation endproducts (AGE) are the result of post-translational changes to proteins, which ultimately compromise their structure and/or function. The identification of methods to prevent the formation of these compounds holds great promise in the development of alternative therapies for di...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482150/ https://www.ncbi.nlm.nih.gov/pubmed/26110531 http://dx.doi.org/10.1371/journal.pone.0131222 |
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author | de Melo, Ingrid Sofia Vieira dos Santos, Aldenir Feitosa de Lemos, Telma Leda Gomes Goulart, Marília Oliveira Fonseca Santana, Antônio Euzébio Goulart |
author_facet | de Melo, Ingrid Sofia Vieira dos Santos, Aldenir Feitosa de Lemos, Telma Leda Gomes Goulart, Marília Oliveira Fonseca Santana, Antônio Euzébio Goulart |
author_sort | de Melo, Ingrid Sofia Vieira |
collection | PubMed |
description | Advanced glycation endproducts (AGE) are the result of post-translational changes to proteins, which ultimately compromise their structure and/or function. The identification of methods to prevent the formation of these compounds holds great promise in the development of alternative therapies for diseases such as diabetes. Plants used in traditional medicine are often rich sources of anti-glycation agents. Therefore, in this study, we investigated the anti-glycation activity of one such compound, Oncocalyxone A (Onco A). Using spectrofluorimetric techniques, we determined that Onco A inhibits AGE formation in a concentration-dependent manner. Its IC(50) value (87.88 ± 3.08 μM) was almost two times lower than the standard anti-glycation compound aminoguanidine (184.68 ± 4.85 μM). The excellent anti-glycation activity of Onco A makes it an exciting candidate for the treatment of diseases associated with excessive accumulation of AGE. However, additional studies are necessary to identify its mechanism of action, as well as the in vivo response in suitable model organisms. |
format | Online Article Text |
id | pubmed-4482150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44821502015-07-01 Oncocalyxone A Functions As an Anti-Glycation Agent In Vitro de Melo, Ingrid Sofia Vieira dos Santos, Aldenir Feitosa de Lemos, Telma Leda Gomes Goulart, Marília Oliveira Fonseca Santana, Antônio Euzébio Goulart PLoS One Research Article Advanced glycation endproducts (AGE) are the result of post-translational changes to proteins, which ultimately compromise their structure and/or function. The identification of methods to prevent the formation of these compounds holds great promise in the development of alternative therapies for diseases such as diabetes. Plants used in traditional medicine are often rich sources of anti-glycation agents. Therefore, in this study, we investigated the anti-glycation activity of one such compound, Oncocalyxone A (Onco A). Using spectrofluorimetric techniques, we determined that Onco A inhibits AGE formation in a concentration-dependent manner. Its IC(50) value (87.88 ± 3.08 μM) was almost two times lower than the standard anti-glycation compound aminoguanidine (184.68 ± 4.85 μM). The excellent anti-glycation activity of Onco A makes it an exciting candidate for the treatment of diseases associated with excessive accumulation of AGE. However, additional studies are necessary to identify its mechanism of action, as well as the in vivo response in suitable model organisms. Public Library of Science 2015-06-25 /pmc/articles/PMC4482150/ /pubmed/26110531 http://dx.doi.org/10.1371/journal.pone.0131222 Text en © 2015 Melo et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article de Melo, Ingrid Sofia Vieira dos Santos, Aldenir Feitosa de Lemos, Telma Leda Gomes Goulart, Marília Oliveira Fonseca Santana, Antônio Euzébio Goulart Oncocalyxone A Functions As an Anti-Glycation Agent In Vitro |
title | Oncocalyxone A Functions As an Anti-Glycation Agent In Vitro |
title_full | Oncocalyxone A Functions As an Anti-Glycation Agent In Vitro |
title_fullStr | Oncocalyxone A Functions As an Anti-Glycation Agent In Vitro |
title_full_unstemmed | Oncocalyxone A Functions As an Anti-Glycation Agent In Vitro |
title_short | Oncocalyxone A Functions As an Anti-Glycation Agent In Vitro |
title_sort | oncocalyxone a functions as an anti-glycation agent in vitro |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482150/ https://www.ncbi.nlm.nih.gov/pubmed/26110531 http://dx.doi.org/10.1371/journal.pone.0131222 |
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