Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107157
DC FieldValueLanguage
dc.contributor.authorCarneiro, Tatiana J.-
dc.contributor.authorAraújo, Rita-
dc.contributor.authorVojtek, Martin-
dc.contributor.authorGonçalves-Monteiro, Salomé-
dc.contributor.authorDiniz, Carmen-
dc.contributor.authorBatista de Carvalho, Ana L. M.-
dc.contributor.authorMarques, Maria Paula-
dc.contributor.authorGil, Ana M-
dc.date.accessioned2023-06-12T10:22:18Z-
dc.date.available2023-06-12T10:22:18Z-
dc.date.issued2019-11-13-
dc.identifier.issn2218-1989-
dc.identifier.urihttps://hdl.handle.net/10316/107157-
dc.description.abstractThis 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.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationUID/CTM/50011/2019pt
dc.relationUID/QUI/50006/2019pt
dc.relationUID/MULTI/ 00070/2019pt
dc.relationPOCI-01-0145-FEDER-0016786pt
dc.relationCentro-01-0145-FEDER-029956pt
dc.relationPD/BD/135460/2017pt
dc.relationPTDC/QEQ-MED/1890/2014pt
dc.relationSFRH/BD/145920/2019pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectcisplatinpt
dc.subjectmicept
dc.subjectmouse modelpt
dc.subjectin vivopt
dc.subjectNMRpt
dc.subjectmetabolomicspt
dc.subjectmetabonomicspt
dc.subjectkidneypt
dc.subjectliverpt
dc.subjectbreast tissuept
dc.titleMulti-Organ NMR Metabolomics to Assess In Vivo Overall Metabolic Impact of Cisplatin in Micept
dc.typearticlept
degois.publication.firstPage279pt
degois.publication.issue11pt
degois.publication.titleMetabolitespt
dc.peerreviewedyespt
dc.identifier.doi10.3390/metabo9110279-
degois.publication.volume9pt
dc.date.embargo2019-11-13*
dc.identifier.pmid31766161-
uc.date.periodoEmbargo0pt
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.openairetypearticle-
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.cerifentitytypePublications-
crisitem.project.grantnoMolecular Physical-Chemistry-
crisitem.author.researchunitCEIS20 - Centre of 20th Century Interdisciplinary Studies-
crisitem.author.researchunitQFM-UC – Molecular Physical-Chemistry R&D Unit-
crisitem.author.researchunitQFM-UC – Molecular Physical-Chemistry R&D Unit-
crisitem.author.orcid0000-0003-1280-3321-
crisitem.author.orcid0000-0002-8391-0055-
Appears in Collections:FCTUC Ciências da Vida - Artigos em Revistas Internacionais
I&D QFM-UC - Artigos em Revistas Internacionais
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This item is licensed under a Creative Commons License Creative Commons