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Pharmacokinetics, Tissue Distribution, Metabolism, and Excretion of Naringin in Aged Rats
Aging is an inevitable biological process characterized by the loss of functional capacity and associated with changes in all phases of pharmacokinetic processes. Naringin, a dietary flavanone glycoside, has been proved to be beneficial for the treatment of multiple age-associated chronic diseases....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362423/ https://www.ncbi.nlm.nih.gov/pubmed/30761003 http://dx.doi.org/10.3389/fphar.2019.00034 |
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author | Zeng, Xuan Su, Weiwei Zheng, Yuying He, Yudong He, Yan Rao, Hongyu Peng, Wei Yao, Hongliang |
author_facet | Zeng, Xuan Su, Weiwei Zheng, Yuying He, Yudong He, Yan Rao, Hongyu Peng, Wei Yao, Hongliang |
author_sort | Zeng, Xuan |
collection | PubMed |
description | Aging is an inevitable biological process characterized by the loss of functional capacity and associated with changes in all phases of pharmacokinetic processes. Naringin, a dietary flavanone glycoside, has been proved to be beneficial for the treatment of multiple age-associated chronic diseases. To date, the pharmacokinetic processes of naringin in aged individuals are still unknown. Thus, a rapid resolution liquid chromatography tandem triple quadrupole mass spectrometry (RRLC-QQQ-MS/MS) method was established for the determination of naringin and its metabolite naringenin in rat plasma, urine, feces, and tissue homogenate. The pharmacokinetic parameters were calculated and a higher exposure of naringin and naringenin were observed in aged rats. Naringin and naringenin were mostly distributed in gastrointestinal tract, liver, kidney, lung, and trachea. Furthermore, a total of 39 flavonoid metabolites (mainly glucuronides and sulfates) and 46 microbial-derived phenolic catabolites were screened with ultra-fast liquid chromatography-quadrupole-time-of-flight tandem mass spectrometry (UFLC-Q-TOF-MS/MS). Naringenin, hippuric acid, and 3-(4’-hydroxyphenyl)propionic acid were predominated metabolites. This study systemically investigated the pharmacokinetics, tissue distribution, metabolism, and excretion of naringin in aged rats, revealing age- and gender-related changes in the in vivo behavior of naringin. These results would be helpful for the interpretation of pharmacokinetics and pharmacodynamics of naringin in aged population. |
format | Online Article Text |
id | pubmed-6362423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63624232019-02-13 Pharmacokinetics, Tissue Distribution, Metabolism, and Excretion of Naringin in Aged Rats Zeng, Xuan Su, Weiwei Zheng, Yuying He, Yudong He, Yan Rao, Hongyu Peng, Wei Yao, Hongliang Front Pharmacol Pharmacology Aging is an inevitable biological process characterized by the loss of functional capacity and associated with changes in all phases of pharmacokinetic processes. Naringin, a dietary flavanone glycoside, has been proved to be beneficial for the treatment of multiple age-associated chronic diseases. To date, the pharmacokinetic processes of naringin in aged individuals are still unknown. Thus, a rapid resolution liquid chromatography tandem triple quadrupole mass spectrometry (RRLC-QQQ-MS/MS) method was established for the determination of naringin and its metabolite naringenin in rat plasma, urine, feces, and tissue homogenate. The pharmacokinetic parameters were calculated and a higher exposure of naringin and naringenin were observed in aged rats. Naringin and naringenin were mostly distributed in gastrointestinal tract, liver, kidney, lung, and trachea. Furthermore, a total of 39 flavonoid metabolites (mainly glucuronides and sulfates) and 46 microbial-derived phenolic catabolites were screened with ultra-fast liquid chromatography-quadrupole-time-of-flight tandem mass spectrometry (UFLC-Q-TOF-MS/MS). Naringenin, hippuric acid, and 3-(4’-hydroxyphenyl)propionic acid were predominated metabolites. This study systemically investigated the pharmacokinetics, tissue distribution, metabolism, and excretion of naringin in aged rats, revealing age- and gender-related changes in the in vivo behavior of naringin. These results would be helpful for the interpretation of pharmacokinetics and pharmacodynamics of naringin in aged population. Frontiers Media S.A. 2019-01-28 /pmc/articles/PMC6362423/ /pubmed/30761003 http://dx.doi.org/10.3389/fphar.2019.00034 Text en Copyright © 2019 Zeng, Su, Zheng, He, He, Rao, Peng and Yao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Zeng, Xuan Su, Weiwei Zheng, Yuying He, Yudong He, Yan Rao, Hongyu Peng, Wei Yao, Hongliang Pharmacokinetics, Tissue Distribution, Metabolism, and Excretion of Naringin in Aged Rats |
title | Pharmacokinetics, Tissue Distribution, Metabolism, and Excretion of Naringin in Aged Rats |
title_full | Pharmacokinetics, Tissue Distribution, Metabolism, and Excretion of Naringin in Aged Rats |
title_fullStr | Pharmacokinetics, Tissue Distribution, Metabolism, and Excretion of Naringin in Aged Rats |
title_full_unstemmed | Pharmacokinetics, Tissue Distribution, Metabolism, and Excretion of Naringin in Aged Rats |
title_short | Pharmacokinetics, Tissue Distribution, Metabolism, and Excretion of Naringin in Aged Rats |
title_sort | pharmacokinetics, tissue distribution, metabolism, and excretion of naringin in aged rats |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362423/ https://www.ncbi.nlm.nih.gov/pubmed/30761003 http://dx.doi.org/10.3389/fphar.2019.00034 |
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