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Multi-Organ NMR Metabolomics to Assess In Vivo Overall Metabolic Impact of Cisplatin in Mice

This work describes, to our knowledge, the first NMR metabolomics analysis of mice kidney, liver, and breast tissue in response to cisplatin exposure, in search of early metabolic signatures of cisplatin biotoxicity. Balb/c mice were exposed to a single 3.5 mg/kg dose of cisplatin and then euthanize...

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Autores principales: Carneiro, Tatiana J., Araújo, Rita, Vojtek, Martin, Gonçalves-Monteiro, Salomé, Diniz, Carmen, Batista de Carvalho, Ana L.M., Marques, Maria Paula M., Gil, Ana M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918135/
https://www.ncbi.nlm.nih.gov/pubmed/31766161
http://dx.doi.org/10.3390/metabo9110279
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author Carneiro, Tatiana J.
Araújo, Rita
Vojtek, Martin
Gonçalves-Monteiro, Salomé
Diniz, Carmen
Batista de Carvalho, Ana L.M.
Marques, Maria Paula M.
Gil, Ana M.
author_facet Carneiro, Tatiana J.
Araújo, Rita
Vojtek, Martin
Gonçalves-Monteiro, Salomé
Diniz, Carmen
Batista de Carvalho, Ana L.M.
Marques, Maria Paula M.
Gil, Ana M.
author_sort Carneiro, Tatiana J.
collection PubMed
description This work describes, to our knowledge, the first NMR metabolomics analysis of mice kidney, liver, and breast tissue in response to cisplatin exposure, in search of early metabolic signatures of cisplatin biotoxicity. Balb/c mice were exposed to a single 3.5 mg/kg dose of cisplatin and then euthanized; organs (kidney, liver, breast tissue) were collected at 1, 12, and 48 h. Polar tissue extracts were analyzed by NMR spectroscopy, and the resulting spectra were studied by multivariate and univariate analyses. The results enabled the identification of the most significant deviant metabolite levels at each time point, and for each tissue type, and showed that the largest metabolic impact occurs for kidney, as early as 1 h post-injection. Kidney tissue showed a marked depletion in several amino acids, comprised in an overall 13-metabolites signature. The highest number of changes in all tissues was noted at 12 h, although many of those recovered to control levels at 48 h, with the exception of some persistently deviant tissue-specific metabolites, thus enabling the identification of relatively longer-term effects of cDDP. This work reports, for the first time, early (1–48 h) concomitant effects of cDDP in kidney, liver, and breast tissue metabolism, thus contributing to the understanding of multi-organ cDDP biotoxicity.
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spelling pubmed-69181352019-12-24 Multi-Organ NMR Metabolomics to Assess In Vivo Overall Metabolic Impact of Cisplatin in Mice Carneiro, Tatiana J. Araújo, Rita Vojtek, Martin Gonçalves-Monteiro, Salomé Diniz, Carmen Batista de Carvalho, Ana L.M. Marques, Maria Paula M. Gil, Ana M. Metabolites Article This work describes, to our knowledge, the first NMR metabolomics analysis of mice kidney, liver, and breast tissue in response to cisplatin exposure, in search of early metabolic signatures of cisplatin biotoxicity. Balb/c mice were exposed to a single 3.5 mg/kg dose of cisplatin and then euthanized; organs (kidney, liver, breast tissue) were collected at 1, 12, and 48 h. Polar tissue extracts were analyzed by NMR spectroscopy, and the resulting spectra were studied by multivariate and univariate analyses. The results enabled the identification of the most significant deviant metabolite levels at each time point, and for each tissue type, and showed that the largest metabolic impact occurs for kidney, as early as 1 h post-injection. Kidney tissue showed a marked depletion in several amino acids, comprised in an overall 13-metabolites signature. The highest number of changes in all tissues was noted at 12 h, although many of those recovered to control levels at 48 h, with the exception of some persistently deviant tissue-specific metabolites, thus enabling the identification of relatively longer-term effects of cDDP. This work reports, for the first time, early (1–48 h) concomitant effects of cDDP in kidney, liver, and breast tissue metabolism, thus contributing to the understanding of multi-organ cDDP biotoxicity. MDPI 2019-11-13 /pmc/articles/PMC6918135/ /pubmed/31766161 http://dx.doi.org/10.3390/metabo9110279 Text en © 2019 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
Carneiro, Tatiana J.
Araújo, Rita
Vojtek, Martin
Gonçalves-Monteiro, Salomé
Diniz, Carmen
Batista de Carvalho, Ana L.M.
Marques, Maria Paula M.
Gil, Ana M.
Multi-Organ NMR Metabolomics to Assess In Vivo Overall Metabolic Impact of Cisplatin in Mice
title Multi-Organ NMR Metabolomics to Assess In Vivo Overall Metabolic Impact of Cisplatin in Mice
title_full Multi-Organ NMR Metabolomics to Assess In Vivo Overall Metabolic Impact of Cisplatin in Mice
title_fullStr Multi-Organ NMR Metabolomics to Assess In Vivo Overall Metabolic Impact of Cisplatin in Mice
title_full_unstemmed Multi-Organ NMR Metabolomics to Assess In Vivo Overall Metabolic Impact of Cisplatin in Mice
title_short Multi-Organ NMR Metabolomics to Assess In Vivo Overall Metabolic Impact of Cisplatin in Mice
title_sort multi-organ nmr metabolomics to assess in vivo overall metabolic impact of cisplatin in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918135/
https://www.ncbi.nlm.nih.gov/pubmed/31766161
http://dx.doi.org/10.3390/metabo9110279
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