Evidence map›Paper›PMID 26208861›Full record

ArticleMalaria journal2015

Plasmodium transmission blocking activities of Vernonia amygdalina extracts and isolated compounds.

Solomon M Abay, Leonardo Lucantoni, Nisha Dahiya, Geme Dori, Edson G Dembo, Fulvio Esposito, Guilio Lupidi, Sonny Ogboi, Robert K Ouédraogo, Annamaria Sinisi and 7 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.6field-weighted citation impact, top 5% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

20 citing papers in PubMed, 61 citations in OpenAlex.

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  9. Medicinal plants as a fight against murine blood-stage malaria.Saudi journal of biological sciences · 2021
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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

17 authors at 4 institutions in 5 countries.

Solomon M AbaySchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. solomonabay@gmail.com.
Leonardo LucantoniSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. l.lucantoni@griffith.edu.au.
Nisha DahiyaSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. nisha.dahiya@unicam.it.
Geme DoriSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. gemeurge@yahoo.com.
Edson G DemboSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. edembo@gmail.com.
Fulvio EspositoSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. fulvio.esposito@unicam.it.
Guilio LupidiSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. giulio.lupidi@unicam.it.
Sonny OgboiSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. ogboijb@yahoo.com.
Robert K OuédraogoSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. oued.kossivi.robert@gmail.com.
Annamaria SinisiDepartment of Pharmacy, University of Naples Federico II, Via Montesano 49, 80131, Naples, Italy. annamaria.sinisi@unina.it.
Orazio Taglialatela-ScafatiDepartment of Pharmacy, University of Naples Federico II, Via Montesano 49, 80131, Naples, Italy. scatagli@unina.it.
R Serge YerbangaInstitut de Recherche enSciences de la Santé, Direction Régionale de l'Ouest, Bobo-Dioulasso, Burkina Faso. yrserge@yahoo.fr.
Massimo BramucciSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. massimo.bramucci@unicam.it.
Luana QuassintiSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. luana.quassinti@unicam.it.
Jean Bosco OuédraogoInstitut de Recherche enSciences de la Santé, Direction Régionale de l'Ouest, Bobo-Dioulasso, Burkina Faso. jbouedraogo@gmail.com.
George ChristophidesDepartment of Life Sciences, Imperial College London, London, UK. g.christophides@imperial.ac.uk.
Annette HabluetzelSchool of Pharmacy, University of Camerino, Piazza dei Costanti, 62032, Camerino, MC, Italy. annette.habluetzel@unicam.it.
Università di Camerino · ITInstitut de Recherche en Sciences de la Santé · BFUniversity of Naples Federico II · ITImperial College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMedicinal plants are a validated source for discovery of new leads and standardized herbal medicines. The aim of this study was to assess the activity of Vernonia amygdalina leaf extracts and isolated compounds against gametocytes and sporogonic stages of Plasmodium berghei and to validate the findings on field isolates of Plasmodium falciparum.

methodsAqueous (Ver-H2O) and ethanolic (Ver-EtOH) leaf extracts were tested in vivo for activity against sexual and asexual blood stage P. berghei parasites. In vivo transmission blocking effects of Ver-EtOH and Ver-H2O were estimated by assessing P. berghei oocyst prevalence and density in Anopheles stephensi mosquitoes. Activity targeting early sporogonic stages (ESS), namely gametes, zygotes and ookinetes was assessed in vitro using P. berghei CTRPp.GFP strain. Bioassay guided fractionation was performed to characterize V. amygdalina fractions and molecules for anti-ESS activity. Fractions active against ESS of the murine parasite were tested for ex vivo transmission blocking activity on P. falciparum field isolates. Cytotoxic effects of extracts and isolated compounds vernolide and vernodalol were evaluated on the human cell lines HCT116 and EA.hy926.

resultsVer-H2O reduced the P. berghei macrogametocyte density in mice by about 50% and Ver-EtOH reduced P. berghei oocyst prevalence and density by 27 and 90%, respectively, in An. stephensi mosquitoes. Ver-EtOH inhibited almost completely (>90%) ESS development in vitro at 50 μg/mL. At this concentration, four fractions obtained from the ethylacetate phase of the methanol extract displayed inhibitory activity >90% against ESS. Three tested fractions were also found active against field isolates of the human parasite P. falciparum, reducing oocyst prevalence in Anopheles coluzzii mosquitoes to one-half and oocyst density to one-fourth of controls. The molecules and fractions displayed considerable cytotoxicity on the two tested cell-lines.

conclusionsVernonia amygdalina leaves contain molecules affecting multiple stages of Plasmodium, evidencing its potential for drug discovery. Chemical modification of the identified hit molecules, in particular vernodalol, could generate a library of druggable sesquiterpene lactones. The development of a multistage phytomedicine designed as preventive treatment to complement existing malaria control tools appears a challenging but feasible goal.

Indexed as

AnimalsAnophelesAntimalarialsCell LineCell SurvivalFemaleHumansMalariaMaleMicePlant ExtractsPlasmodium bergheiVernoniaAntimalarialsPlant Extracts

Identifiers

PMID26208861
PMCPMC4513948
OpenAlexW1708413965

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.