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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
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.
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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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