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Structures of Astaxanthin and Their Consequences for Therapeutic Application
Reactive oxygen species (ROS) are continuously generated as a by-product of normal aerobic metabolism. Elevated ROS formation leads to potential damage of biological structures and is implicated in various diseases. Astaxanthin, a xanthophyll carotenoid, is a secondary metabolite responsible for the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391096/ https://www.ncbi.nlm.nih.gov/pubmed/32775406 http://dx.doi.org/10.1155/2020/2156582 |
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author | Brotosudarmo, Tatas Hardo Panintingjati Limantara, Leenawaty Setiyono, Edi Heriyanto, |
author_facet | Brotosudarmo, Tatas Hardo Panintingjati Limantara, Leenawaty Setiyono, Edi Heriyanto, |
author_sort | Brotosudarmo, Tatas Hardo Panintingjati |
collection | PubMed |
description | Reactive oxygen species (ROS) are continuously generated as a by-product of normal aerobic metabolism. Elevated ROS formation leads to potential damage of biological structures and is implicated in various diseases. Astaxanthin, a xanthophyll carotenoid, is a secondary metabolite responsible for the red-orange color of a number of marine animals and microorganisms. There is mounting evidence that astaxanthin has powerful antioxidant, anti-inflammatory, and antiapoptotic activities. Hence, its consumption can result in various health benefits, with potential for therapeutic application. Astaxanthin contains both a hydroxyl and a keto group, and this unique structure plays important roles in neutralizing ROS. The molecule quenches harmful singlet oxygen, scavenges peroxyl and hydroxyl radicals and converts them into more stable compounds, prevents the formation of free radicals, and inhibits the autoxidation chain reaction. It also acts as a metal chelator and converts metal prooxidants into harmless molecules. However, like many other carotenoids, astaxanthin is affected by the environmental conditions, e.g., pH, heat, or exposure to light. It is hence susceptible to structural modification, i.e., via isomerization, aggregation, or esterification, which alters its physiochemical properties. Here, we provide a concise overview of the distribution of astaxanthin in tissues, and astaxanthin structures, and their role in tackling singlet oxygen and free radicals. We highlight the effect of structural modification of astaxanthin molecules on the bioavailability and biological activity. These studies suggested that astaxanthin would be a promising dietary supplement for health applications. |
format | Online Article Text |
id | pubmed-7391096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-73910962020-08-06 Structures of Astaxanthin and Their Consequences for Therapeutic Application Brotosudarmo, Tatas Hardo Panintingjati Limantara, Leenawaty Setiyono, Edi Heriyanto, Int J Food Sci Review Article Reactive oxygen species (ROS) are continuously generated as a by-product of normal aerobic metabolism. Elevated ROS formation leads to potential damage of biological structures and is implicated in various diseases. Astaxanthin, a xanthophyll carotenoid, is a secondary metabolite responsible for the red-orange color of a number of marine animals and microorganisms. There is mounting evidence that astaxanthin has powerful antioxidant, anti-inflammatory, and antiapoptotic activities. Hence, its consumption can result in various health benefits, with potential for therapeutic application. Astaxanthin contains both a hydroxyl and a keto group, and this unique structure plays important roles in neutralizing ROS. The molecule quenches harmful singlet oxygen, scavenges peroxyl and hydroxyl radicals and converts them into more stable compounds, prevents the formation of free radicals, and inhibits the autoxidation chain reaction. It also acts as a metal chelator and converts metal prooxidants into harmless molecules. However, like many other carotenoids, astaxanthin is affected by the environmental conditions, e.g., pH, heat, or exposure to light. It is hence susceptible to structural modification, i.e., via isomerization, aggregation, or esterification, which alters its physiochemical properties. Here, we provide a concise overview of the distribution of astaxanthin in tissues, and astaxanthin structures, and their role in tackling singlet oxygen and free radicals. We highlight the effect of structural modification of astaxanthin molecules on the bioavailability and biological activity. These studies suggested that astaxanthin would be a promising dietary supplement for health applications. Hindawi 2020-07-20 /pmc/articles/PMC7391096/ /pubmed/32775406 http://dx.doi.org/10.1155/2020/2156582 Text en Copyright © 2020 Tatas Hardo Panintingjati Brotosudarmo et al. http://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 Brotosudarmo, Tatas Hardo Panintingjati Limantara, Leenawaty Setiyono, Edi Heriyanto, Structures of Astaxanthin and Their Consequences for Therapeutic Application |
title | Structures of Astaxanthin and Their Consequences for Therapeutic Application |
title_full | Structures of Astaxanthin and Their Consequences for Therapeutic Application |
title_fullStr | Structures of Astaxanthin and Their Consequences for Therapeutic Application |
title_full_unstemmed | Structures of Astaxanthin and Their Consequences for Therapeutic Application |
title_short | Structures of Astaxanthin and Their Consequences for Therapeutic Application |
title_sort | structures of astaxanthin and their consequences for therapeutic application |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391096/ https://www.ncbi.nlm.nih.gov/pubmed/32775406 http://dx.doi.org/10.1155/2020/2156582 |
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