Cargando…
Direct Implementation of Intestinal Permeability Test in NMR Metabolomics for Simultaneous Biomarker Discovery—A Feasibility Study in a Preterm Piglet Model
Measurement of intestinal permeability (IP) is often used in the examination of inflammatory gastrointestinal disorders. IP can be assessed by measurement of urinary recovery of ingested non-metabolizable lactulose (L) and mannitol (M). The present study aimed to examine how measurements of IP can b...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022985/ https://www.ncbi.nlm.nih.gov/pubmed/31906404 http://dx.doi.org/10.3390/metabo10010022 |
_version_ | 1783498144145735680 |
---|---|
author | Alinaghi, Masoumeh Nguyen, Duc Ninh Sangild, Per Torp Bertram, Hanne Christine |
author_facet | Alinaghi, Masoumeh Nguyen, Duc Ninh Sangild, Per Torp Bertram, Hanne Christine |
author_sort | Alinaghi, Masoumeh |
collection | PubMed |
description | Measurement of intestinal permeability (IP) is often used in the examination of inflammatory gastrointestinal disorders. IP can be assessed by measurement of urinary recovery of ingested non-metabolizable lactulose (L) and mannitol (M). The present study aimed to examine how measurements of IP can be integrated in a NMR-based metabolomics approach for a simultaneous quantification of L/M ratio and biomarker exploration. For this purpose, plasma and urine samples were collected from five-day-old preterm piglets (n = 20) with gastrointestinal disorders (subjected to intra-amniotic lipopolysaccharide (LPS, 1 mg/fetus)) after they had been administrated a 5% lactulose and 5% mannitol solution (15 mL/kg). The collected plasma and urine samples were analyzed by (1)H NMR-based metabolomics. Urine L/M ratio measured by (1)H NMR spectroscopy showed high correlation with the standard measurement of the urinary recoveries by enzymatic assays (r = 0.93, p < 0.05). Partial least squares (PLS) regressions and correlation analyses between L/M ratio and NMR metabolomics data revealed that L/M ratio was positively correlated with plasma lactate, acetate and succinate levels and negatively correlated with urinary hippuric acid and glycine. In conclusion, the present study demonstrated that NMR metabolomics enables simultaneous IP testing and discovery of biomarkers associated with an impaired intestinal permeability. |
format | Online Article Text |
id | pubmed-7022985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70229852020-03-12 Direct Implementation of Intestinal Permeability Test in NMR Metabolomics for Simultaneous Biomarker Discovery—A Feasibility Study in a Preterm Piglet Model Alinaghi, Masoumeh Nguyen, Duc Ninh Sangild, Per Torp Bertram, Hanne Christine Metabolites Article Measurement of intestinal permeability (IP) is often used in the examination of inflammatory gastrointestinal disorders. IP can be assessed by measurement of urinary recovery of ingested non-metabolizable lactulose (L) and mannitol (M). The present study aimed to examine how measurements of IP can be integrated in a NMR-based metabolomics approach for a simultaneous quantification of L/M ratio and biomarker exploration. For this purpose, plasma and urine samples were collected from five-day-old preterm piglets (n = 20) with gastrointestinal disorders (subjected to intra-amniotic lipopolysaccharide (LPS, 1 mg/fetus)) after they had been administrated a 5% lactulose and 5% mannitol solution (15 mL/kg). The collected plasma and urine samples were analyzed by (1)H NMR-based metabolomics. Urine L/M ratio measured by (1)H NMR spectroscopy showed high correlation with the standard measurement of the urinary recoveries by enzymatic assays (r = 0.93, p < 0.05). Partial least squares (PLS) regressions and correlation analyses between L/M ratio and NMR metabolomics data revealed that L/M ratio was positively correlated with plasma lactate, acetate and succinate levels and negatively correlated with urinary hippuric acid and glycine. In conclusion, the present study demonstrated that NMR metabolomics enables simultaneous IP testing and discovery of biomarkers associated with an impaired intestinal permeability. MDPI 2020-01-01 /pmc/articles/PMC7022985/ /pubmed/31906404 http://dx.doi.org/10.3390/metabo10010022 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Alinaghi, Masoumeh Nguyen, Duc Ninh Sangild, Per Torp Bertram, Hanne Christine Direct Implementation of Intestinal Permeability Test in NMR Metabolomics for Simultaneous Biomarker Discovery—A Feasibility Study in a Preterm Piglet Model |
title | Direct Implementation of Intestinal Permeability Test in NMR Metabolomics for Simultaneous Biomarker Discovery—A Feasibility Study in a Preterm Piglet Model |
title_full | Direct Implementation of Intestinal Permeability Test in NMR Metabolomics for Simultaneous Biomarker Discovery—A Feasibility Study in a Preterm Piglet Model |
title_fullStr | Direct Implementation of Intestinal Permeability Test in NMR Metabolomics for Simultaneous Biomarker Discovery—A Feasibility Study in a Preterm Piglet Model |
title_full_unstemmed | Direct Implementation of Intestinal Permeability Test in NMR Metabolomics for Simultaneous Biomarker Discovery—A Feasibility Study in a Preterm Piglet Model |
title_short | Direct Implementation of Intestinal Permeability Test in NMR Metabolomics for Simultaneous Biomarker Discovery—A Feasibility Study in a Preterm Piglet Model |
title_sort | direct implementation of intestinal permeability test in nmr metabolomics for simultaneous biomarker discovery—a feasibility study in a preterm piglet model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022985/ https://www.ncbi.nlm.nih.gov/pubmed/31906404 http://dx.doi.org/10.3390/metabo10010022 |
work_keys_str_mv | AT alinaghimasoumeh directimplementationofintestinalpermeabilitytestinnmrmetabolomicsforsimultaneousbiomarkerdiscoveryafeasibilitystudyinapretermpigletmodel AT nguyenducninh directimplementationofintestinalpermeabilitytestinnmrmetabolomicsforsimultaneousbiomarkerdiscoveryafeasibilitystudyinapretermpigletmodel AT sangildpertorp directimplementationofintestinalpermeabilitytestinnmrmetabolomicsforsimultaneousbiomarkerdiscoveryafeasibilitystudyinapretermpigletmodel AT bertramhannechristine directimplementationofintestinalpermeabilitytestinnmrmetabolomicsforsimultaneousbiomarkerdiscoveryafeasibilitystudyinapretermpigletmodel |