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Effect of a soluble prebiotic fiber, NUTRIOSE, on the absorption of ginsenoside Rd in rats orally administered ginseng
BACKGROUND: There is limited understanding of the effect of dietary components on the absorption of ginsenosides and their metabolites into the blood. METHODS: This study investigated the pharmacokinetics of the ginseng extract and its main constituent ginsenoside Rb1 in rats with or without pretrea...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213839/ https://www.ncbi.nlm.nih.gov/pubmed/25378995 http://dx.doi.org/10.1016/j.jgr.2014.03.003 |
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author | Kim, Kyung-Ah Yoo, Hye Hyun Gu, Wan Yu, Dae-Hyung Jin, Ming Ji Choi, Hae-Lim Yuan, Kathy Guerin-Deremaux, Laetitia Kim, Dong-Hyun |
author_facet | Kim, Kyung-Ah Yoo, Hye Hyun Gu, Wan Yu, Dae-Hyung Jin, Ming Ji Choi, Hae-Lim Yuan, Kathy Guerin-Deremaux, Laetitia Kim, Dong-Hyun |
author_sort | Kim, Kyung-Ah |
collection | PubMed |
description | BACKGROUND: There is limited understanding of the effect of dietary components on the absorption of ginsenosides and their metabolites into the blood. METHODS: This study investigated the pharmacokinetics of the ginseng extract and its main constituent ginsenoside Rb1 in rats with or without pretreatment with a prebiotic fiber, NUTRIOSE, by liquid chromatography tandem mass spectrometry. When ginsenoside Rb1 was incubated with rat feces, its main metabolite was ginsenoside Rd. RESULTS: When the intestinal microbiota of rat feces were cultured in vitro, their ginsenoside Rd-forming activities were significantly induced by NUTRIOSE. When ginsenoside Rb1 was orally administered to rats, the maximum plasma concentration (Cmax) and area under the plasma drug concentration–time curve (AUC) for the main metabolite, ginsenoside Rd, were 72.4 ± 31.6 ng/mL and 663.9 ± 285.3 μg·h/mL, respectively. When the ginseng extract (2,000 mg/kg) was orally administered, Cmax and AUC for ginsenoside Rd were 906.5 ± 330.2 ng/mL and 11,377.3 ± 4,470.2 μg·h/mL, respectively. When ginseng extract was orally administered to rats fed NUTRIOSE containing diets (2.5%, 5%, or 10%), Cmax and AUC were increased in the NUTRIOSE receiving groups in a dose-dependent manner. CONCLUSION: These findings reveal that intestinal microflora promote metabolic conversion of ginsenoside Rb1 and ginseng extract to ginsenoside Rd and promote its absorption into the blood in rats. Its conversion may be induced by prebiotic diets such as NUTRIOSE. |
format | Online Article Text |
id | pubmed-4213839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-42138392014-11-06 Effect of a soluble prebiotic fiber, NUTRIOSE, on the absorption of ginsenoside Rd in rats orally administered ginseng Kim, Kyung-Ah Yoo, Hye Hyun Gu, Wan Yu, Dae-Hyung Jin, Ming Ji Choi, Hae-Lim Yuan, Kathy Guerin-Deremaux, Laetitia Kim, Dong-Hyun J Ginseng Res Research Article BACKGROUND: There is limited understanding of the effect of dietary components on the absorption of ginsenosides and their metabolites into the blood. METHODS: This study investigated the pharmacokinetics of the ginseng extract and its main constituent ginsenoside Rb1 in rats with or without pretreatment with a prebiotic fiber, NUTRIOSE, by liquid chromatography tandem mass spectrometry. When ginsenoside Rb1 was incubated with rat feces, its main metabolite was ginsenoside Rd. RESULTS: When the intestinal microbiota of rat feces were cultured in vitro, their ginsenoside Rd-forming activities were significantly induced by NUTRIOSE. When ginsenoside Rb1 was orally administered to rats, the maximum plasma concentration (Cmax) and area under the plasma drug concentration–time curve (AUC) for the main metabolite, ginsenoside Rd, were 72.4 ± 31.6 ng/mL and 663.9 ± 285.3 μg·h/mL, respectively. When the ginseng extract (2,000 mg/kg) was orally administered, Cmax and AUC for ginsenoside Rd were 906.5 ± 330.2 ng/mL and 11,377.3 ± 4,470.2 μg·h/mL, respectively. When ginseng extract was orally administered to rats fed NUTRIOSE containing diets (2.5%, 5%, or 10%), Cmax and AUC were increased in the NUTRIOSE receiving groups in a dose-dependent manner. CONCLUSION: These findings reveal that intestinal microflora promote metabolic conversion of ginsenoside Rb1 and ginseng extract to ginsenoside Rd and promote its absorption into the blood in rats. Its conversion may be induced by prebiotic diets such as NUTRIOSE. 2014-04-21 2014-07 /pmc/articles/PMC4213839/ /pubmed/25378995 http://dx.doi.org/10.1016/j.jgr.2014.03.003 Text en © 2014 The Korean Society of Ginseng. Published by Elsevier B.V. All rights reserved. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the CC-BY-NC License (http://creativecommons.org/licenses/by-nc/3.0). |
spellingShingle | Research Article Kim, Kyung-Ah Yoo, Hye Hyun Gu, Wan Yu, Dae-Hyung Jin, Ming Ji Choi, Hae-Lim Yuan, Kathy Guerin-Deremaux, Laetitia Kim, Dong-Hyun Effect of a soluble prebiotic fiber, NUTRIOSE, on the absorption of ginsenoside Rd in rats orally administered ginseng |
title | Effect of a soluble prebiotic fiber, NUTRIOSE, on the absorption of ginsenoside Rd in rats orally administered ginseng |
title_full | Effect of a soluble prebiotic fiber, NUTRIOSE, on the absorption of ginsenoside Rd in rats orally administered ginseng |
title_fullStr | Effect of a soluble prebiotic fiber, NUTRIOSE, on the absorption of ginsenoside Rd in rats orally administered ginseng |
title_full_unstemmed | Effect of a soluble prebiotic fiber, NUTRIOSE, on the absorption of ginsenoside Rd in rats orally administered ginseng |
title_short | Effect of a soluble prebiotic fiber, NUTRIOSE, on the absorption of ginsenoside Rd in rats orally administered ginseng |
title_sort | effect of a soluble prebiotic fiber, nutriose, on the absorption of ginsenoside rd in rats orally administered ginseng |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213839/ https://www.ncbi.nlm.nih.gov/pubmed/25378995 http://dx.doi.org/10.1016/j.jgr.2014.03.003 |
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