Publication
A Simple, label-free, and high-throughput method to evaluate the epigallocatechin-3-gallate impact in plasma molecular profile
dc.contributor.author | Araújo, Rúben | |
dc.contributor.author | Ramalhete, Luís | |
dc.contributor.author | Da Paz, Helder | |
dc.contributor.author | Ribeiro, Edna | |
dc.contributor.author | Calado, Cecília | |
dc.date.accessioned | 2020-07-31T15:00:21Z | |
dc.date.available | 2020-07-31T15:00:21Z | |
dc.date.issued | 2020-04-09 | |
dc.description | Este trabalho foi financiado pelo Concurso Anual para Projetos de Investigação, Desenvolvimento, Inovação e Criação Artística (IDI&CA) 2016 do Instituto Politécnico de Lisboa. Código de referência IPL/2018/RENALPROG_ISEL | |
dc.description.abstract | Epigallocatechin-3-gallate (EGCG), the major catechin presente in green tea, presents diverse appealing biological activities, such as antioxidative, anti-inflammatory, antimicrobial, and antiviral activities, among others. The present work evaluated the impact in the molecular profile of human plasma from daily consumption of 225 mg of EGCG for 90 days. Plasma from peripheral blood was collected from 30 healthy human volunteers and analyzed by high-throughput Fourier transform infrared spectroscopy. To capture the biochemical information while minimizing the interference of physical phenomena, several combinations of spectra pre-processing methods were evaluated by principal component analysis. The pre-processing method that led to the best class separation, that is, between the plasma spectral data collected at the beginning and after the 90 days, was a combination of atmospheric correction with a second derivative spectra. A hierarchical cluster analysis of second derivativespectraalsohighlightedthefactthatplasmaacquiredbeforeEGCGconsumptionpresented a distinct molecular profile after the 90 days of EGCG consumption. It was also possible by partial least squares regression discriminant analysis to correctly predict all unlabeled plasma samples (not used for model construction) at both timeframes. We observed that the similarity in composition among the plasma samples was higher in samples collected after EGCG consumption when compared with the samples taken prior to EGCG consumption. Diverse negative peaks of the normalized second derivative spectra, associated with lipid and protein regions, were significantly affected (p < 0.001) by EGCG consumption, according to the impact of EGCG consumption on the patients’ blood, low density and high density lipoproteins ratio. In conclusion, a single bolus dose of 225 mg of EGCG, ingested throughout a period of 90 days, drastically affected plasma molecular composition in all participants, which raises awareness regarding prolonged human exposure to EGCG. Because the analysis was conducted in a high-throughput, label-free, and economic analysis, it could be applied to high-dimension molecular epidemiological studies to further promote the understanding of the effect of bio-compound consumption mode and frequency. | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | ARAÚJO, Rúben; [et al] – A Simple, label-free, and high-throughput method to evaluate the epigallocatechin-3-gallate impact in plasma molecular profile. High-Throughput. ISSN 2571-5135. Vol. 9, N.º 2 (2020), pp. 1-12 | pt_PT |
dc.identifier.doi | 10.3390/ht9020009 | pt_PT |
dc.identifier.issn | 2571-5135 | |
dc.identifier.uri | http://hdl.handle.net/10400.21/12132 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | MDPI | pt_PT |
dc.relation | Projeto financiado no âmbito do Concurso de Projetos de Investigação, Desenvolvimento, Inovação & Criação Artística (IDI&CA) financiados pelo Instituto Politécnico de Lisboa. IPL/2018/RENALPROG_ISEL | pt_PT |
dc.relation.publisherversion | https://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC7349803&blobtype=pdf | pt_PT |
dc.subject | High-throughput | pt_PT |
dc.subject | FTIR spectroscopy | pt_PT |
dc.subject | EGCG | pt_PT |
dc.subject | Plasma | pt_PT |
dc.title | A Simple, label-free, and high-throughput method to evaluate the epigallocatechin-3-gallate impact in plasma molecular profile | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.endPage | 12 | pt_PT |
oaire.citation.issue | 2 | pt_PT |
oaire.citation.startPage | 1 | pt_PT |
oaire.citation.title | High-Throughput | pt_PT |
oaire.citation.volume | 9 | pt_PT |
person.familyName | Araújo | |
person.familyName | Ramalhete | |
person.familyName | Da Paz | |
person.familyName | Ribeiro | |
person.familyName | Calado | |
person.givenName | Rúben Alexandre Dinis | |
person.givenName | Luís | |
person.givenName | Helder | |
person.givenName | Edna | |
person.givenName | Cecília | |
person.identifier | 2296066 | |
person.identifier | 130332 | |
person.identifier.ciencia-id | 9A18-BFDC-ED95 | |
person.identifier.ciencia-id | DF19-022D-AA10 | |
person.identifier.ciencia-id | C414-CDF2-D35A | |
person.identifier.ciencia-id | 9418-E320-3177 | |
person.identifier.orcid | 0000-0002-9369-6486 | |
person.identifier.orcid | 0000-0002-8911-3380 | |
person.identifier.orcid | 0000-0003-1749-9605 | |
person.identifier.orcid | 0000-0003-1316-7750 | |
person.identifier.orcid | 0000-0002-5264-9755 | |
person.identifier.rid | E-2102-2014 | |
person.identifier.scopus-author-id | 57208672678 | |
person.identifier.scopus-author-id | 6603163260 | |
rcaap.rights | openAccess | pt_PT |
rcaap.type | article | pt_PT |
relation.isAuthorOfPublication | 9998e940-5e65-4661-8308-afcb56d5df01 | |
relation.isAuthorOfPublication | 7846e088-851e-47b6-a7bd-d02c9d8f047d | |
relation.isAuthorOfPublication | 5473e051-c0a8-4452-acd9-4c8692c03218 | |
relation.isAuthorOfPublication | a571bf34-bcda-49ca-b5cb-4cdecbb3d9c7 | |
relation.isAuthorOfPublication | e8577257-c64c-4481-9b2b-940fedb360cc | |
relation.isAuthorOfPublication.latestForDiscovery | 5473e051-c0a8-4452-acd9-4c8692c03218 |
Files
Original bundle
1 - 1 of 1
No Thumbnail Available
- Name:
- A simple_CRCCalado.pdf
- Size:
- 2.06 MB
- Format:
- Adobe Portable Document Format