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Effect of insect tea on D‐galactose‐induced oxidation in mice and its mechanisms
Insect tea is a traditional Chinese drink that contains abundant bioactive substances. In this study, the preventive effect of Insect tea on D‐galactose‐induced oxidation in mice was studied. The serum, liver, and spleen of mice were measured by biochemical and molecular biological methods, which sh...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6924339/ https://www.ncbi.nlm.nih.gov/pubmed/31890190 http://dx.doi.org/10.1002/fsn3.1278 |
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author | Zhu, Kai Zeng, Xiaofei Tan, Fang Li, Wenfeng Li, Chong Song, Yaru Zhao, Xin |
author_facet | Zhu, Kai Zeng, Xiaofei Tan, Fang Li, Wenfeng Li, Chong Song, Yaru Zhao, Xin |
author_sort | Zhu, Kai |
collection | PubMed |
description | Insect tea is a traditional Chinese drink that contains abundant bioactive substances. In this study, the preventive effect of Insect tea on D‐galactose‐induced oxidation in mice was studied. The serum, liver, and spleen of mice were measured by biochemical and molecular biological methods, which showed that Insect tea could increase the biochemical indexes of the thymus, brain, heart, liver, spleen, and kidney in mice with induced oxidative damage. Insect tea can increase the levels of SOD (superoxide dismutase), GSH‐Px (glutathione peroxidase), and GSH (glutathione) and decrease the levels of MDA (malondialdehyde) in the serum, liver, and spleen of mice with oxidative damage. Pathological observation also confirmed that Insect tea could inhibit oxidative damage of the liver and spleen tissue caused by D‐galactose in mice. Further molecular biological experiments also showed that Insect tea could upregulate the mRNA and protein expression of Cu/Zn‐SOD (cuprozinc‐superoxide dismutase), Mn‐SOD (manganese superoxide dismutase), CAT (catalase), HO‐1 (heme oxygenase‐1), Nrf2 (nuclear factor‐erythroid 2 related factor 2), γ‐GCS (γ‐glutamylcysteine synthetase), and NQO1 (NAD(P)H dehydrogenase [quinone] 1) in the liver and spleen of oxidized mice. Insect tea has a good preventive effect on D‐galactose‐induced oxidation in mice, and the effect is better than vitamin C, an antioxidant. Insect tea is rich in isochlorogenic acid A, quercetin, rutin, hesperidin, neochlorogenic acid, and cryptochlorogenic acid. The combination of these bioactive substances has good antioxidant effects. Thus, Insect tea is a functional food with a good antioxidant effect that has value for future development and utilization. |
format | Online Article Text |
id | pubmed-6924339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69243392019-12-30 Effect of insect tea on D‐galactose‐induced oxidation in mice and its mechanisms Zhu, Kai Zeng, Xiaofei Tan, Fang Li, Wenfeng Li, Chong Song, Yaru Zhao, Xin Food Sci Nutr Original Research Insect tea is a traditional Chinese drink that contains abundant bioactive substances. In this study, the preventive effect of Insect tea on D‐galactose‐induced oxidation in mice was studied. The serum, liver, and spleen of mice were measured by biochemical and molecular biological methods, which showed that Insect tea could increase the biochemical indexes of the thymus, brain, heart, liver, spleen, and kidney in mice with induced oxidative damage. Insect tea can increase the levels of SOD (superoxide dismutase), GSH‐Px (glutathione peroxidase), and GSH (glutathione) and decrease the levels of MDA (malondialdehyde) in the serum, liver, and spleen of mice with oxidative damage. Pathological observation also confirmed that Insect tea could inhibit oxidative damage of the liver and spleen tissue caused by D‐galactose in mice. Further molecular biological experiments also showed that Insect tea could upregulate the mRNA and protein expression of Cu/Zn‐SOD (cuprozinc‐superoxide dismutase), Mn‐SOD (manganese superoxide dismutase), CAT (catalase), HO‐1 (heme oxygenase‐1), Nrf2 (nuclear factor‐erythroid 2 related factor 2), γ‐GCS (γ‐glutamylcysteine synthetase), and NQO1 (NAD(P)H dehydrogenase [quinone] 1) in the liver and spleen of oxidized mice. Insect tea has a good preventive effect on D‐galactose‐induced oxidation in mice, and the effect is better than vitamin C, an antioxidant. Insect tea is rich in isochlorogenic acid A, quercetin, rutin, hesperidin, neochlorogenic acid, and cryptochlorogenic acid. The combination of these bioactive substances has good antioxidant effects. Thus, Insect tea is a functional food with a good antioxidant effect that has value for future development and utilization. John Wiley and Sons Inc. 2019-11-17 /pmc/articles/PMC6924339/ /pubmed/31890190 http://dx.doi.org/10.1002/fsn3.1278 Text en © 2019 The Authors. Food Science & Nutrition published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Zhu, Kai Zeng, Xiaofei Tan, Fang Li, Wenfeng Li, Chong Song, Yaru Zhao, Xin Effect of insect tea on D‐galactose‐induced oxidation in mice and its mechanisms |
title | Effect of insect tea on D‐galactose‐induced oxidation in mice and its mechanisms |
title_full | Effect of insect tea on D‐galactose‐induced oxidation in mice and its mechanisms |
title_fullStr | Effect of insect tea on D‐galactose‐induced oxidation in mice and its mechanisms |
title_full_unstemmed | Effect of insect tea on D‐galactose‐induced oxidation in mice and its mechanisms |
title_short | Effect of insect tea on D‐galactose‐induced oxidation in mice and its mechanisms |
title_sort | effect of insect tea on d‐galactose‐induced oxidation in mice and its mechanisms |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6924339/ https://www.ncbi.nlm.nih.gov/pubmed/31890190 http://dx.doi.org/10.1002/fsn3.1278 |
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