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- PMID: 25911822
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Article: Urine metabonomic study on long-term use of total ginsenosides in rats
Title | Urine metabonomic study on long-term use of total ginsenosides in rats |
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Authors | |
Issue Date | 2014 |
Citation | Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 2014, v. 39, n. 23, p. 4675-4679 How to Cite? |
Abstract | Due to its effect of systems regulation and promotion on body, Ginseng is always referred to be long-term used as a dietary supplement. But it was still unclear about its target of the tonic effects and also the side-effects long-term use may bring. Urine metabolomic method is suitable for long-term studies of pharmaco-dynamics, pharmacology and toxicology of traditional Chinese medicine because of its characteristics of non-invasive and monitoring the whole-body metabolism. This study was designed to detect the dynamic variation of rat urine metabolome along with a long-term administration of total ginsenosides using GC-TOF based metabolomic technology. Our result showed that either short-term or chronic administration of ginsenosides did not impact the rat urine metabolome significantly (as the PCA subgroup was not successful). By comparison, the short-term (1-3 w) dose of ginsenosides had the biggest metabolic influence including TCA cycle, catecholamines and neurotransmitter amino acids. Medium-term (6-10 w) dose had a gradually lower effect and long-term (27 w) dose almost had no effect. Our study indicates that both short and long-term administration of ginsenosides showed almost no obvious side-effect on the experimental animals. |
Persistent Identifier | http://hdl.handle.net/10722/342491 |
ISSN | 2023 SCImago Journal Rankings: 0.206 |
DC Field | Value | Language |
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dc.contributor.author | Xie, Xie | - |
dc.contributor.author | Chen, Shao Qiu | - |
dc.contributor.author | Lv, Ying Fang | - |
dc.contributor.author | Wang, Xiao Yan | - |
dc.contributor.author | Jia, Wei | - |
dc.date.accessioned | 2024-04-17T07:04:11Z | - |
dc.date.available | 2024-04-17T07:04:11Z | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 2014, v. 39, n. 23, p. 4675-4679 | - |
dc.identifier.issn | 1001-5302 | - |
dc.identifier.uri | http://hdl.handle.net/10722/342491 | - |
dc.description.abstract | Due to its effect of systems regulation and promotion on body, Ginseng is always referred to be long-term used as a dietary supplement. But it was still unclear about its target of the tonic effects and also the side-effects long-term use may bring. Urine metabolomic method is suitable for long-term studies of pharmaco-dynamics, pharmacology and toxicology of traditional Chinese medicine because of its characteristics of non-invasive and monitoring the whole-body metabolism. This study was designed to detect the dynamic variation of rat urine metabolome along with a long-term administration of total ginsenosides using GC-TOF based metabolomic technology. Our result showed that either short-term or chronic administration of ginsenosides did not impact the rat urine metabolome significantly (as the PCA subgroup was not successful). By comparison, the short-term (1-3 w) dose of ginsenosides had the biggest metabolic influence including TCA cycle, catecholamines and neurotransmitter amino acids. Medium-term (6-10 w) dose had a gradually lower effect and long-term (27 w) dose almost had no effect. Our study indicates that both short and long-term administration of ginsenosides showed almost no obvious side-effect on the experimental animals. | - |
dc.language | eng | - |
dc.relation.ispartof | Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica | - |
dc.title | Urine metabonomic study on long-term use of total ginsenosides in rats | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.pmid | 25911822 | - |
dc.identifier.scopus | eid_2-s2.0-84930802725 | - |
dc.identifier.volume | 39 | - |
dc.identifier.issue | 23 | - |
dc.identifier.spage | 4675 | - |
dc.identifier.epage | 4679 | - |