Evidence map›Paper›PMID 30830463›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2019

Phenolic variation among Chamaecrista nictitans subspecies and varieties revealed through UPLC-ESI(-)-MS/MS chemical fingerprinting.

Luis Quirós-Guerrero, Federico Albertazzi, Emanuel Araya-Valverde, Rosaura M Romero, Heidy Villalobos, Luis Poveda, Max Chavarría, Giselle Tamayo-Castillo

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Article in Metabolomics : Official journal of the Metabolomic Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Constituents ofPharmaceutics · 2021
    Article
  2. Article
  3. Plants (Basel, Switzerland) · 2020
    Article
  4. Predictive Modeling for Metabolomics Data.Methods in molecular biology (Clifton, N.J.) · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Luis Quirós-GuerreroCentro de Investigaciones en Productos Naturales (CIPRONA), Universidad de Costa Rica, San Jose, 11501-2060, Costa Rica.
Federico AlbertazziCentro de Investigación en Biología Celular y Molecular (CIBCM), Universidad de Costa Rica, San Jose, 11501-2060, Costa Rica.
Emanuel Araya-ValverdeCentro Nacional de Innovaciones Biotecnológicas (CENiBiot), CeNAT-CONARE, San Jose, 1174-1200, Costa Rica.
Rosaura M RomeroCentro de Investigaciones en Productos Naturales (CIPRONA), Universidad de Costa Rica, San Jose, 11501-2060, Costa Rica.
Heidy VillalobosEscuela de Química, Universidad de Costa Rica, Sede Central, San Pedro de Montes de Oca, San Jose, 11501-2060, Costa Rica.
Luis PovedaHerbario Juvenal Valerio Rodríguez, Universidad Nacional, Heredia, Costa Rica.
Max ChavarríaCentro de Investigaciones en Productos Naturales (CIPRONA), Universidad de Costa Rica, San Jose, 11501-2060, Costa Rica.
Giselle Tamayo-CastilloCentro de Investigaciones en Productos Naturales (CIPRONA), Universidad de Costa Rica, San Jose, 11501-2060, Costa Rica. giselle.tamayo@ucr.ac.cr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionComparative analysis of metabolic features of plants has a high potential for determination of quality control of active ingredients, ecological or chemotaxonomic purposes. Specifically, the development of efficient and rapid analytical tools that allow the differentiation among species, subspecies and varieties of plants is a relevant issue. Here we describe a multivariate model based on LC-MS/MS fingerprinting capable of discriminating between subspecies and varieties of the medicinal plant Chamaecrista nictitans, a rare distributed species in Costa Rica.

methodsDetermination of the chemical fingerprint was carried out on a LC-MS (ESI-QTOF) in negative ionization mode, main detected and putatively identified compounds included proanthocyanidin oligomers, several flavonoid C- and O-glycosides, and flavonoid acetates. Principal component analysis (PCA), partial least square-discriminant analysis (PLS-DA) and cluster analysis of chemical profiles were performed.

resultsOur method showed a clear discrimination between the subspecies and varieties of Chamaecrista nictitans, separating the samples into four fair differentiated groups: M1 = C. nictitans ssp. patellaria; M2 = C. nictitans ssp. disadena; M3 = C. nictitans ssp. nictitans var. jaliscensis and M4 = C. nictitans ssp. disadena var. pilosa. LC-MS/MS fingerprint data was validated using both morphological characters and DNA barcoding with ITS2 region. The comparison of the morphological characters against the chemical profiles and DNA barcoding shows a 63% coincidence, evidencing the morphological similarity in C. nictitans. On the other hand, genetic data and chemical profiles grouped all samples in a similar pattern, validating the functionality of our metabolomic approach.

conclusionThe metabolomic method described in this study allows a reliably differentiation between subspecies and varieties of C. nictitans using a straightforward protocol that lacks extensive purification steps.

Indexed as

ChamaecristaChromatography, High Pressure LiquidChromatography, LiquidCluster AnalysisDiscriminant AnalysisMetabolomicsMultivariate AnalysisPhenolsPrincipal Component AnalysisSpectrometry, Mass, Electrospray IonizationTandem Mass SpectrometryPhenolsChamaecrista nictitansChemical fingerprintingChemotaxonomyLC–MS/MSMetabolite fingerprinting

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.