Cargando…

Aspirin eugenol ester regulates cecal contents metabolomic profile and microbiota in an animal model of hyperlipidemia

BACKGROUND: Hyperlipidemia, with an increasing of prevalence, has become one of the common metabolic diseases in companion animal clinic. Aspirin eugenol ester (AEE) is a novel compound that exhibits efficacious anti-hyperlipidemia activities. However, its mechanisms are still not completely known....

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Ning, Liu, Xi-Wang, Kong, Xiao-Jun, Li, Shi-Hong, Jiao, Zeng-Hua, Qin, Zhe, Yang, Ya-Jun, Li, Jian-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299661/
https://www.ncbi.nlm.nih.gov/pubmed/30563510
http://dx.doi.org/10.1186/s12917-018-1711-x
_version_ 1783381533945495552
author Ma, Ning
Liu, Xi-Wang
Kong, Xiao-Jun
Li, Shi-Hong
Jiao, Zeng-Hua
Qin, Zhe
Yang, Ya-Jun
Li, Jian-Yong
author_facet Ma, Ning
Liu, Xi-Wang
Kong, Xiao-Jun
Li, Shi-Hong
Jiao, Zeng-Hua
Qin, Zhe
Yang, Ya-Jun
Li, Jian-Yong
author_sort Ma, Ning
collection PubMed
description BACKGROUND: Hyperlipidemia, with an increasing of prevalence, has become one of the common metabolic diseases in companion animal clinic. Aspirin eugenol ester (AEE) is a novel compound that exhibits efficacious anti-hyperlipidemia activities. However, its mechanisms are still not completely known. The objective of present study was to investigate the intervention effects of AEE on cecal contents metabonomics profile and microbiota in hyperlipidemia rats. RESULTS: Three groups of rats were fed with a control diet, or high fat diet (HFD) containing or not AEE. The results showed the beneficial effects of AEE in HFD-fed rats such as the reducing of aspartate aminotransferase (AST) and total cholesterol (TCH). Distinct changes in metabonomics profile of cecal contents were observed among control, model and AEE groups. HFD-induced alterations of eight metabolites in cecal contents mainly related with purine metabolism, linoleic acid metabolism, glycerophospholipid metabolism, sphingolipid metabolism and pyrimidine metabolism were reversed by AEE treatment. Principal coordinate analysis (PCoA) and cluster analysis of microbiota showed altered patterns with distinct differences in AEE group versus model group, indicating that AEE treatment improved the negative effects caused by HFD on cecal microbiota. In addition, the correction analysis revealed the possible link between the identified metabolites and cecal microbiota. CONCLUSIONS: This study showed regulation effects of AEE on cecal contents metabonomics profile and microbiota, which could provide information to reveal the possible underlying mechanism of AEE on hyperlipidemia treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12917-018-1711-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6299661
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-62996612018-12-20 Aspirin eugenol ester regulates cecal contents metabolomic profile and microbiota in an animal model of hyperlipidemia Ma, Ning Liu, Xi-Wang Kong, Xiao-Jun Li, Shi-Hong Jiao, Zeng-Hua Qin, Zhe Yang, Ya-Jun Li, Jian-Yong BMC Vet Res Research Article BACKGROUND: Hyperlipidemia, with an increasing of prevalence, has become one of the common metabolic diseases in companion animal clinic. Aspirin eugenol ester (AEE) is a novel compound that exhibits efficacious anti-hyperlipidemia activities. However, its mechanisms are still not completely known. The objective of present study was to investigate the intervention effects of AEE on cecal contents metabonomics profile and microbiota in hyperlipidemia rats. RESULTS: Three groups of rats were fed with a control diet, or high fat diet (HFD) containing or not AEE. The results showed the beneficial effects of AEE in HFD-fed rats such as the reducing of aspartate aminotransferase (AST) and total cholesterol (TCH). Distinct changes in metabonomics profile of cecal contents were observed among control, model and AEE groups. HFD-induced alterations of eight metabolites in cecal contents mainly related with purine metabolism, linoleic acid metabolism, glycerophospholipid metabolism, sphingolipid metabolism and pyrimidine metabolism were reversed by AEE treatment. Principal coordinate analysis (PCoA) and cluster analysis of microbiota showed altered patterns with distinct differences in AEE group versus model group, indicating that AEE treatment improved the negative effects caused by HFD on cecal microbiota. In addition, the correction analysis revealed the possible link between the identified metabolites and cecal microbiota. CONCLUSIONS: This study showed regulation effects of AEE on cecal contents metabonomics profile and microbiota, which could provide information to reveal the possible underlying mechanism of AEE on hyperlipidemia treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12917-018-1711-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-18 /pmc/articles/PMC6299661/ /pubmed/30563510 http://dx.doi.org/10.1186/s12917-018-1711-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ma, Ning
Liu, Xi-Wang
Kong, Xiao-Jun
Li, Shi-Hong
Jiao, Zeng-Hua
Qin, Zhe
Yang, Ya-Jun
Li, Jian-Yong
Aspirin eugenol ester regulates cecal contents metabolomic profile and microbiota in an animal model of hyperlipidemia
title Aspirin eugenol ester regulates cecal contents metabolomic profile and microbiota in an animal model of hyperlipidemia
title_full Aspirin eugenol ester regulates cecal contents metabolomic profile and microbiota in an animal model of hyperlipidemia
title_fullStr Aspirin eugenol ester regulates cecal contents metabolomic profile and microbiota in an animal model of hyperlipidemia
title_full_unstemmed Aspirin eugenol ester regulates cecal contents metabolomic profile and microbiota in an animal model of hyperlipidemia
title_short Aspirin eugenol ester regulates cecal contents metabolomic profile and microbiota in an animal model of hyperlipidemia
title_sort aspirin eugenol ester regulates cecal contents metabolomic profile and microbiota in an animal model of hyperlipidemia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299661/
https://www.ncbi.nlm.nih.gov/pubmed/30563510
http://dx.doi.org/10.1186/s12917-018-1711-x
work_keys_str_mv AT maning aspirineugenolesterregulatescecalcontentsmetabolomicprofileandmicrobiotainananimalmodelofhyperlipidemia
AT liuxiwang aspirineugenolesterregulatescecalcontentsmetabolomicprofileandmicrobiotainananimalmodelofhyperlipidemia
AT kongxiaojun aspirineugenolesterregulatescecalcontentsmetabolomicprofileandmicrobiotainananimalmodelofhyperlipidemia
AT lishihong aspirineugenolesterregulatescecalcontentsmetabolomicprofileandmicrobiotainananimalmodelofhyperlipidemia
AT jiaozenghua aspirineugenolesterregulatescecalcontentsmetabolomicprofileandmicrobiotainananimalmodelofhyperlipidemia
AT qinzhe aspirineugenolesterregulatescecalcontentsmetabolomicprofileandmicrobiotainananimalmodelofhyperlipidemia
AT yangyajun aspirineugenolesterregulatescecalcontentsmetabolomicprofileandmicrobiotainananimalmodelofhyperlipidemia
AT lijianyong aspirineugenolesterregulatescecalcontentsmetabolomicprofileandmicrobiotainananimalmodelofhyperlipidemia