Cargando…

Longitudinal Metabolomics and Lipidomics Analyses Reveal Alterations Associated with Envenoming by Bothrops asper and Daboia russelii in an Experimental Murine Model

Longitudinal metabolomics and lipidomics analyses were carried out on the blood plasma of mice injected intramuscularly with venoms of the viperid species Bothrops asper or Daboia russelii. Blood samples were collected 1, 3, 6, and 24 h after venom injection, and a control group of non-envenomed mic...

Descripción completa

Detalles Bibliográficos
Autores principales: Wase, Nishikant, Gutiérrez, José María, Rucavado, Alexandra, Fox, Jay W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610966/
https://www.ncbi.nlm.nih.gov/pubmed/36287926
http://dx.doi.org/10.3390/toxins14100657
_version_ 1784819409681907712
author Wase, Nishikant
Gutiérrez, José María
Rucavado, Alexandra
Fox, Jay W.
author_facet Wase, Nishikant
Gutiérrez, José María
Rucavado, Alexandra
Fox, Jay W.
author_sort Wase, Nishikant
collection PubMed
description Longitudinal metabolomics and lipidomics analyses were carried out on the blood plasma of mice injected intramuscularly with venoms of the viperid species Bothrops asper or Daboia russelii. Blood samples were collected 1, 3, 6, and 24 h after venom injection, and a control group of non-envenomed mice was included. Significant perturbations in metabolomics and lipidomics were observed at 1, 3, and 6 h, while values returned close to those of control mice by 24 h, hence reflecting a transient pattern of metabolic disturbance. Both venoms induced significant changes in amino acids, as well as in several purines and pyrimidines, and in some metabolites of the tricarboxylic acid cycle. KEGG analysis of metabolic pathways that showed those with the greatest change included aminoacyl tRNA synthesis and amino acid biosynthesis and metabolism pathways. With regard to lipid metabolism, there was an increase in triglycerides and some acyl carnitines and a concomitant drop in the levels of some phospholipids. In addition, envenomed mice had higher levels of cortisol, heme, and some oxidative stress markers. The overall pattern of metabolic changes in envenomed mice bears similarities with the patterns described in several traumatic injuries, thus underscoring a metabolic response/adaptation to the injurious action of the venoms.
format Online
Article
Text
id pubmed-9610966
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96109662022-10-28 Longitudinal Metabolomics and Lipidomics Analyses Reveal Alterations Associated with Envenoming by Bothrops asper and Daboia russelii in an Experimental Murine Model Wase, Nishikant Gutiérrez, José María Rucavado, Alexandra Fox, Jay W. Toxins (Basel) Article Longitudinal metabolomics and lipidomics analyses were carried out on the blood plasma of mice injected intramuscularly with venoms of the viperid species Bothrops asper or Daboia russelii. Blood samples were collected 1, 3, 6, and 24 h after venom injection, and a control group of non-envenomed mice was included. Significant perturbations in metabolomics and lipidomics were observed at 1, 3, and 6 h, while values returned close to those of control mice by 24 h, hence reflecting a transient pattern of metabolic disturbance. Both venoms induced significant changes in amino acids, as well as in several purines and pyrimidines, and in some metabolites of the tricarboxylic acid cycle. KEGG analysis of metabolic pathways that showed those with the greatest change included aminoacyl tRNA synthesis and amino acid biosynthesis and metabolism pathways. With regard to lipid metabolism, there was an increase in triglycerides and some acyl carnitines and a concomitant drop in the levels of some phospholipids. In addition, envenomed mice had higher levels of cortisol, heme, and some oxidative stress markers. The overall pattern of metabolic changes in envenomed mice bears similarities with the patterns described in several traumatic injuries, thus underscoring a metabolic response/adaptation to the injurious action of the venoms. MDPI 2022-09-23 /pmc/articles/PMC9610966/ /pubmed/36287926 http://dx.doi.org/10.3390/toxins14100657 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wase, Nishikant
Gutiérrez, José María
Rucavado, Alexandra
Fox, Jay W.
Longitudinal Metabolomics and Lipidomics Analyses Reveal Alterations Associated with Envenoming by Bothrops asper and Daboia russelii in an Experimental Murine Model
title Longitudinal Metabolomics and Lipidomics Analyses Reveal Alterations Associated with Envenoming by Bothrops asper and Daboia russelii in an Experimental Murine Model
title_full Longitudinal Metabolomics and Lipidomics Analyses Reveal Alterations Associated with Envenoming by Bothrops asper and Daboia russelii in an Experimental Murine Model
title_fullStr Longitudinal Metabolomics and Lipidomics Analyses Reveal Alterations Associated with Envenoming by Bothrops asper and Daboia russelii in an Experimental Murine Model
title_full_unstemmed Longitudinal Metabolomics and Lipidomics Analyses Reveal Alterations Associated with Envenoming by Bothrops asper and Daboia russelii in an Experimental Murine Model
title_short Longitudinal Metabolomics and Lipidomics Analyses Reveal Alterations Associated with Envenoming by Bothrops asper and Daboia russelii in an Experimental Murine Model
title_sort longitudinal metabolomics and lipidomics analyses reveal alterations associated with envenoming by bothrops asper and daboia russelii in an experimental murine model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610966/
https://www.ncbi.nlm.nih.gov/pubmed/36287926
http://dx.doi.org/10.3390/toxins14100657
work_keys_str_mv AT wasenishikant longitudinalmetabolomicsandlipidomicsanalysesrevealalterationsassociatedwithenvenomingbybothropsasperanddaboiarusseliiinanexperimentalmurinemodel
AT gutierrezjosemaria longitudinalmetabolomicsandlipidomicsanalysesrevealalterationsassociatedwithenvenomingbybothropsasperanddaboiarusseliiinanexperimentalmurinemodel
AT rucavadoalexandra longitudinalmetabolomicsandlipidomicsanalysesrevealalterationsassociatedwithenvenomingbybothropsasperanddaboiarusseliiinanexperimentalmurinemodel
AT foxjayw longitudinalmetabolomicsandlipidomicsanalysesrevealalterationsassociatedwithenvenomingbybothropsasperanddaboiarusseliiinanexperimentalmurinemodel