Cargando…

Identification of the Perturbed Metabolic Pathways Associating With Renal Fibrosis and Evaluating Metabolome Changes of Pretreatment With Astragalus polysaccharide Through Liquid Chromatography Quadrupole Time-Of-Flight Mass Spectrometry

Renal fibrosis is glomerulosclerosis and renal tubulointerstitial fibrosis caused by the increase of interstitial cells and intercellular substances and the accumulation of extracellular matrix, and is a common pathological manifestation of renal disease progressing to end-stage renal failure. It ha...

Descripción completa

Detalles Bibliográficos
Autores principales: Ren, Lei, Guo, Xiao-Ying, Gao, Fei, Jin, Mei-Li, Song, Xiang-Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000425/
https://www.ncbi.nlm.nih.gov/pubmed/32063847
http://dx.doi.org/10.3389/fphar.2019.01623
_version_ 1783494039306240000
author Ren, Lei
Guo, Xiao-Ying
Gao, Fei
Jin, Mei-Li
Song, Xiang-Nan
author_facet Ren, Lei
Guo, Xiao-Ying
Gao, Fei
Jin, Mei-Li
Song, Xiang-Nan
author_sort Ren, Lei
collection PubMed
description Renal fibrosis is glomerulosclerosis and renal tubulointerstitial fibrosis caused by the increase of interstitial cells and intercellular substances and the accumulation of extracellular matrix, and is a common pathological manifestation of renal disease progressing to end-stage renal failure. It has proved that Astragalus polysaccharide (AP) has curative effect on renal disease; however, its therapeutic mechanism on renal fibrosis is still unclear. Metabolomics approach provides an opportunity to identify novel molecular biomarkers. The purpose of this study is to study the changes of serum metabolic profile of rats with unilateral tubal ligation and replication of renal fibrosis model and the therapeutic effect of AP on it. The blood samples of rats in the control group, renal fibrosis model group, and AP treatment group collected on the 21st day were analyzed by metabolomics method based on UPLC-Q-TOF-MS. Principal component analysis (PCA) showed that clustering was obvious and significantly separated, and paired partial least squares discriminant analysis (OPLS-DA) was used for further analysis. Combined with the network databases such as HMDB and KEGG and a large number of literatures, 32 potential biomarkers related to renal fibrosis were preliminarily screened out and further verified by MS/MS secondary debris information. After pretreatment with AP, 20 biomarkers were significantly regulated, and correlated with phenylalanine, tyrosine, and tryptophan biosynthesis, phenylalanine metabolism, arachidonic acid metabolism, etc. It also revealed the metabolic changes of renal fibrosis and intervention effect of AP. These data uncover a link between metabolism and the molecular mechanism with potential implications in the understanding of the intervention effect of AP. Conclusively, UPLC-Q-TOF-MS–based metabolomics can be valuable and promising strategy to understand the disease mechanism and natural drug pretreatment.
format Online
Article
Text
id pubmed-7000425
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-70004252020-02-14 Identification of the Perturbed Metabolic Pathways Associating With Renal Fibrosis and Evaluating Metabolome Changes of Pretreatment With Astragalus polysaccharide Through Liquid Chromatography Quadrupole Time-Of-Flight Mass Spectrometry Ren, Lei Guo, Xiao-Ying Gao, Fei Jin, Mei-Li Song, Xiang-Nan Front Pharmacol Pharmacology Renal fibrosis is glomerulosclerosis and renal tubulointerstitial fibrosis caused by the increase of interstitial cells and intercellular substances and the accumulation of extracellular matrix, and is a common pathological manifestation of renal disease progressing to end-stage renal failure. It has proved that Astragalus polysaccharide (AP) has curative effect on renal disease; however, its therapeutic mechanism on renal fibrosis is still unclear. Metabolomics approach provides an opportunity to identify novel molecular biomarkers. The purpose of this study is to study the changes of serum metabolic profile of rats with unilateral tubal ligation and replication of renal fibrosis model and the therapeutic effect of AP on it. The blood samples of rats in the control group, renal fibrosis model group, and AP treatment group collected on the 21st day were analyzed by metabolomics method based on UPLC-Q-TOF-MS. Principal component analysis (PCA) showed that clustering was obvious and significantly separated, and paired partial least squares discriminant analysis (OPLS-DA) was used for further analysis. Combined with the network databases such as HMDB and KEGG and a large number of literatures, 32 potential biomarkers related to renal fibrosis were preliminarily screened out and further verified by MS/MS secondary debris information. After pretreatment with AP, 20 biomarkers were significantly regulated, and correlated with phenylalanine, tyrosine, and tryptophan biosynthesis, phenylalanine metabolism, arachidonic acid metabolism, etc. It also revealed the metabolic changes of renal fibrosis and intervention effect of AP. These data uncover a link between metabolism and the molecular mechanism with potential implications in the understanding of the intervention effect of AP. Conclusively, UPLC-Q-TOF-MS–based metabolomics can be valuable and promising strategy to understand the disease mechanism and natural drug pretreatment. Frontiers Media S.A. 2020-01-29 /pmc/articles/PMC7000425/ /pubmed/32063847 http://dx.doi.org/10.3389/fphar.2019.01623 Text en Copyright © 2020 Ren, Guo, Gao, Jin and Song 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
Ren, Lei
Guo, Xiao-Ying
Gao, Fei
Jin, Mei-Li
Song, Xiang-Nan
Identification of the Perturbed Metabolic Pathways Associating With Renal Fibrosis and Evaluating Metabolome Changes of Pretreatment With Astragalus polysaccharide Through Liquid Chromatography Quadrupole Time-Of-Flight Mass Spectrometry
title Identification of the Perturbed Metabolic Pathways Associating With Renal Fibrosis and Evaluating Metabolome Changes of Pretreatment With Astragalus polysaccharide Through Liquid Chromatography Quadrupole Time-Of-Flight Mass Spectrometry
title_full Identification of the Perturbed Metabolic Pathways Associating With Renal Fibrosis and Evaluating Metabolome Changes of Pretreatment With Astragalus polysaccharide Through Liquid Chromatography Quadrupole Time-Of-Flight Mass Spectrometry
title_fullStr Identification of the Perturbed Metabolic Pathways Associating With Renal Fibrosis and Evaluating Metabolome Changes of Pretreatment With Astragalus polysaccharide Through Liquid Chromatography Quadrupole Time-Of-Flight Mass Spectrometry
title_full_unstemmed Identification of the Perturbed Metabolic Pathways Associating With Renal Fibrosis and Evaluating Metabolome Changes of Pretreatment With Astragalus polysaccharide Through Liquid Chromatography Quadrupole Time-Of-Flight Mass Spectrometry
title_short Identification of the Perturbed Metabolic Pathways Associating With Renal Fibrosis and Evaluating Metabolome Changes of Pretreatment With Astragalus polysaccharide Through Liquid Chromatography Quadrupole Time-Of-Flight Mass Spectrometry
title_sort identification of the perturbed metabolic pathways associating with renal fibrosis and evaluating metabolome changes of pretreatment with astragalus polysaccharide through liquid chromatography quadrupole time-of-flight mass spectrometry
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000425/
https://www.ncbi.nlm.nih.gov/pubmed/32063847
http://dx.doi.org/10.3389/fphar.2019.01623
work_keys_str_mv AT renlei identificationoftheperturbedmetabolicpathwaysassociatingwithrenalfibrosisandevaluatingmetabolomechangesofpretreatmentwithastragaluspolysaccharidethroughliquidchromatographyquadrupoletimeofflightmassspectrometry
AT guoxiaoying identificationoftheperturbedmetabolicpathwaysassociatingwithrenalfibrosisandevaluatingmetabolomechangesofpretreatmentwithastragaluspolysaccharidethroughliquidchromatographyquadrupoletimeofflightmassspectrometry
AT gaofei identificationoftheperturbedmetabolicpathwaysassociatingwithrenalfibrosisandevaluatingmetabolomechangesofpretreatmentwithastragaluspolysaccharidethroughliquidchromatographyquadrupoletimeofflightmassspectrometry
AT jinmeili identificationoftheperturbedmetabolicpathwaysassociatingwithrenalfibrosisandevaluatingmetabolomechangesofpretreatmentwithastragaluspolysaccharidethroughliquidchromatographyquadrupoletimeofflightmassspectrometry
AT songxiangnan identificationoftheperturbedmetabolicpathwaysassociatingwithrenalfibrosisandevaluatingmetabolomechangesofpretreatmentwithastragaluspolysaccharidethroughliquidchromatographyquadrupoletimeofflightmassspectrometry