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Cyanidin-3-O-glucoside: Physical-Chemistry, Foodomics and Health Effects
Anthocyanins (ACNs) are plant secondary metabolites from the flavonoid family. Red to blue fruits are major dietary sources of ACNs (up to 1 g/100 g FW), being cyanidin-3-O-glucoside (Cy3G) one of the most widely distributed. Cy3G confers a red hue to fruits, but its content in raspberries and straw...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273591/ https://www.ncbi.nlm.nih.gov/pubmed/27657039 http://dx.doi.org/10.3390/molecules21091264 |
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author | Olivas-Aguirre, Francisco J. Rodrigo-García, Joaquín Martínez-Ruiz, Nina del R. Cárdenas-Robles, Arely I. Mendoza-Díaz, Sandra O. Álvarez-Parrilla, Emilio González-Aguilar, Gustavo A. de la Rosa, Laura A. Ramos-Jiménez, Arnulfo Wall-Medrano, Abraham |
author_facet | Olivas-Aguirre, Francisco J. Rodrigo-García, Joaquín Martínez-Ruiz, Nina del R. Cárdenas-Robles, Arely I. Mendoza-Díaz, Sandra O. Álvarez-Parrilla, Emilio González-Aguilar, Gustavo A. de la Rosa, Laura A. Ramos-Jiménez, Arnulfo Wall-Medrano, Abraham |
author_sort | Olivas-Aguirre, Francisco J. |
collection | PubMed |
description | Anthocyanins (ACNs) are plant secondary metabolites from the flavonoid family. Red to blue fruits are major dietary sources of ACNs (up to 1 g/100 g FW), being cyanidin-3-O-glucoside (Cy3G) one of the most widely distributed. Cy3G confers a red hue to fruits, but its content in raspberries and strawberries is low. It has a good radical scavenging capacity (RSC) against superoxide but not hydroxyl radicals, and its oxidative potential is pH-dependent (58 mV/pH unit). After intake, Cy3G can be metabolized (phases I, II) by oral epithelial cells, absorbed by the gastric epithelium (1%–10%) and it is gut-transformed (phase II & microbial metabolism), reaching the bloodstream (<1%) and urine (about 0.02%) in low amounts. In humans and Caco-2 cells, Cy3G’s major metabolites are protocatechuic acid and phloroglucinaldehyde which are also subjected to entero-hepatic recycling, although caffeic acid and peonidin-3-glucoside seem to be strictly produced in the large bowel and renal tissues. Solid evidence supports Cy3G’s bioactivity as DNA-RSC, gastro protective, anti-inflammatory, anti-thrombotic chemo-preventive and as an epigenetic factor, exerting protection against Helicobacter pylori infection, age-related diseases, type 2 diabetes, cardiovascular disease, metabolic syndrome and oral cancer. Most relevant mechanisms include RSC, epigenetic action, competitive protein-binding and enzyme inhibition. These and other novel aspects on Cy3G’s physical-chemistry, foodomics, and health effects are discussed. |
format | Online Article Text |
id | pubmed-6273591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62735912018-12-28 Cyanidin-3-O-glucoside: Physical-Chemistry, Foodomics and Health Effects Olivas-Aguirre, Francisco J. Rodrigo-García, Joaquín Martínez-Ruiz, Nina del R. Cárdenas-Robles, Arely I. Mendoza-Díaz, Sandra O. Álvarez-Parrilla, Emilio González-Aguilar, Gustavo A. de la Rosa, Laura A. Ramos-Jiménez, Arnulfo Wall-Medrano, Abraham Molecules Review Anthocyanins (ACNs) are plant secondary metabolites from the flavonoid family. Red to blue fruits are major dietary sources of ACNs (up to 1 g/100 g FW), being cyanidin-3-O-glucoside (Cy3G) one of the most widely distributed. Cy3G confers a red hue to fruits, but its content in raspberries and strawberries is low. It has a good radical scavenging capacity (RSC) against superoxide but not hydroxyl radicals, and its oxidative potential is pH-dependent (58 mV/pH unit). After intake, Cy3G can be metabolized (phases I, II) by oral epithelial cells, absorbed by the gastric epithelium (1%–10%) and it is gut-transformed (phase II & microbial metabolism), reaching the bloodstream (<1%) and urine (about 0.02%) in low amounts. In humans and Caco-2 cells, Cy3G’s major metabolites are protocatechuic acid and phloroglucinaldehyde which are also subjected to entero-hepatic recycling, although caffeic acid and peonidin-3-glucoside seem to be strictly produced in the large bowel and renal tissues. Solid evidence supports Cy3G’s bioactivity as DNA-RSC, gastro protective, anti-inflammatory, anti-thrombotic chemo-preventive and as an epigenetic factor, exerting protection against Helicobacter pylori infection, age-related diseases, type 2 diabetes, cardiovascular disease, metabolic syndrome and oral cancer. Most relevant mechanisms include RSC, epigenetic action, competitive protein-binding and enzyme inhibition. These and other novel aspects on Cy3G’s physical-chemistry, foodomics, and health effects are discussed. MDPI 2016-09-21 /pmc/articles/PMC6273591/ /pubmed/27657039 http://dx.doi.org/10.3390/molecules21091264 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Olivas-Aguirre, Francisco J. Rodrigo-García, Joaquín Martínez-Ruiz, Nina del R. Cárdenas-Robles, Arely I. Mendoza-Díaz, Sandra O. Álvarez-Parrilla, Emilio González-Aguilar, Gustavo A. de la Rosa, Laura A. Ramos-Jiménez, Arnulfo Wall-Medrano, Abraham Cyanidin-3-O-glucoside: Physical-Chemistry, Foodomics and Health Effects |
title | Cyanidin-3-O-glucoside: Physical-Chemistry, Foodomics and Health Effects |
title_full | Cyanidin-3-O-glucoside: Physical-Chemistry, Foodomics and Health Effects |
title_fullStr | Cyanidin-3-O-glucoside: Physical-Chemistry, Foodomics and Health Effects |
title_full_unstemmed | Cyanidin-3-O-glucoside: Physical-Chemistry, Foodomics and Health Effects |
title_short | Cyanidin-3-O-glucoside: Physical-Chemistry, Foodomics and Health Effects |
title_sort | cyanidin-3-o-glucoside: physical-chemistry, foodomics and health effects |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273591/ https://www.ncbi.nlm.nih.gov/pubmed/27657039 http://dx.doi.org/10.3390/molecules21091264 |
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