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Persistent hyperammonia and altered concentrations of urea cycle metabolites in a 5-day swine experiment of sepsis
We measured plasma and cerebrospinal fluid (CSF) metabolite concentrations in a 5-day porcine sepsis model of fecal peritonitis. The objectives were: (i) to verify whether the expected pathways that had emerged in previous studies pertain only to the early inflammatory response or persist for the su...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445921/ https://www.ncbi.nlm.nih.gov/pubmed/34531431 http://dx.doi.org/10.1038/s41598-021-97855-7 |
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author | Ferrario, Manuela Pastorelli, Roberta Brunelli, Laura Liu, Shengchen Zanella do Amaral Campos, Pedro Paulo Casoni, Daniela Z’Graggen, Werner J. Jakob, Stephan M. |
author_facet | Ferrario, Manuela Pastorelli, Roberta Brunelli, Laura Liu, Shengchen Zanella do Amaral Campos, Pedro Paulo Casoni, Daniela Z’Graggen, Werner J. Jakob, Stephan M. |
author_sort | Ferrario, Manuela |
collection | PubMed |
description | We measured plasma and cerebrospinal fluid (CSF) metabolite concentrations in a 5-day porcine sepsis model of fecal peritonitis. The objectives were: (i) to verify whether the expected pathways that had emerged in previous studies pertain only to the early inflammatory response or persist for the subsequent days; (ii) to identify metabolic derangements that arise later; (iii) to verify whether CSF metabolite concentrations were altered and if these alterations were similar to those in the blood or delayed. We observed an early response to inflammation and cytokine storms with alterations in lipid and glucose metabolism. The arginine/asymmetric dimethylarginine (ADMA) and phenylalanine/tyrosine balances changed 24 h after resuscitation in plasma, and later in CSF. There was a rise in ammonia concentration, with altered concentrations of metabolites in the urea cycle. Whether persistent derangement of these pathways have a role not only on short-term outcomes but also on longer-term comorbidities, such as septic encephalopathy, should be addressed in further studies. |
format | Online Article Text |
id | pubmed-8445921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84459212021-09-20 Persistent hyperammonia and altered concentrations of urea cycle metabolites in a 5-day swine experiment of sepsis Ferrario, Manuela Pastorelli, Roberta Brunelli, Laura Liu, Shengchen Zanella do Amaral Campos, Pedro Paulo Casoni, Daniela Z’Graggen, Werner J. Jakob, Stephan M. Sci Rep Article We measured plasma and cerebrospinal fluid (CSF) metabolite concentrations in a 5-day porcine sepsis model of fecal peritonitis. The objectives were: (i) to verify whether the expected pathways that had emerged in previous studies pertain only to the early inflammatory response or persist for the subsequent days; (ii) to identify metabolic derangements that arise later; (iii) to verify whether CSF metabolite concentrations were altered and if these alterations were similar to those in the blood or delayed. We observed an early response to inflammation and cytokine storms with alterations in lipid and glucose metabolism. The arginine/asymmetric dimethylarginine (ADMA) and phenylalanine/tyrosine balances changed 24 h after resuscitation in plasma, and later in CSF. There was a rise in ammonia concentration, with altered concentrations of metabolites in the urea cycle. Whether persistent derangement of these pathways have a role not only on short-term outcomes but also on longer-term comorbidities, such as septic encephalopathy, should be addressed in further studies. Nature Publishing Group UK 2021-09-16 /pmc/articles/PMC8445921/ /pubmed/34531431 http://dx.doi.org/10.1038/s41598-021-97855-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ferrario, Manuela Pastorelli, Roberta Brunelli, Laura Liu, Shengchen Zanella do Amaral Campos, Pedro Paulo Casoni, Daniela Z’Graggen, Werner J. Jakob, Stephan M. Persistent hyperammonia and altered concentrations of urea cycle metabolites in a 5-day swine experiment of sepsis |
title | Persistent hyperammonia and altered concentrations of urea cycle metabolites in a 5-day swine experiment of sepsis |
title_full | Persistent hyperammonia and altered concentrations of urea cycle metabolites in a 5-day swine experiment of sepsis |
title_fullStr | Persistent hyperammonia and altered concentrations of urea cycle metabolites in a 5-day swine experiment of sepsis |
title_full_unstemmed | Persistent hyperammonia and altered concentrations of urea cycle metabolites in a 5-day swine experiment of sepsis |
title_short | Persistent hyperammonia and altered concentrations of urea cycle metabolites in a 5-day swine experiment of sepsis |
title_sort | persistent hyperammonia and altered concentrations of urea cycle metabolites in a 5-day swine experiment of sepsis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445921/ https://www.ncbi.nlm.nih.gov/pubmed/34531431 http://dx.doi.org/10.1038/s41598-021-97855-7 |
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