Evidence map›Paper›PMID 27649682›Full record

ArticleMalaria journal2016

Natural products from Zanthoxylum heitzii with potent activity against the malaria parasite.

Christopher Dean Goodman, Ingvild Austarheim, Vanessa Mollard, Bertin Mikolo, Karl Egil Malterud, Geoffrey I McFadden, Helle Wangensteen

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Malaria journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

  1. Activity of the genusFrontiers in pharmacology · 2022
    Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Review
  7. Antimalarial Natural Products.Progress in the chemistry of organic natural products · 2022
    Article
  8. Review
  9. Review
  10. Article
  11. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 3 countries.

Christopher Dean GoodmanSchool of BioSciences, University of Melbourne, Parkville, VIC, 3010, Australia.
Ingvild AustarheimDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of Oslo, P. O. Box 1068, Blindern, 0316, Oslo, Norway.
Vanessa MollardSchool of BioSciences, University of Melbourne, Parkville, VIC, 3010, Australia.
Bertin MikoloNational Polytechnic High School, Marien Ngouabi University, BP 69, Brazzaville, Republic of Congo.
Karl Egil MalterudDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of Oslo, P. O. Box 1068, Blindern, 0316, Oslo, Norway.
Geoffrey I McFaddenSchool of BioSciences, University of Melbourne, Parkville, VIC, 3010, Australia.
Helle WangensteenDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of Oslo, P. O. Box 1068, Blindern, 0316, Oslo, Norway. helle.wangensteen@farmasi.uio.no.
University of Melbourne · AUUniversity of Oslo · NOMarien Ngouabi University · CG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundZanthoxylum heitzii (Rutaceae) (olon) is used in traditional medicine in Central and West Africa to treat malaria. To identify novel compounds with anti-parasitic activity and validate medicinal usage, extracts and compounds isolated from this tree were tested against the erythrocytic stages of the human malaria parasite Plasmodium falciparum and for inhibition of transmission in rodent malaria parasite Plasmodium berghei.

resultsHexane bark extract showed activity against P. falciparum (IC50 0.050 μg/ml), while leaf and seed extracts were inactive. Fractionation of the hexane bark extract led to the identification of three active constituents; dihydronitidine, pellitorine and heitziquinone. Dihydronitidine was the most active compound with an IC50 value of 0.0089 µg/ml (25 nM). This compound was slow acting, requiring 50 % longer exposure time than standard anti-malarials to reach full efficacy. Heitziquinone and pellitorine were less potent, with IC50 values of 3.55 μg/ml and 1.96 µg/ml, but were fast-acting. Plasmodium berghei ookinete conversion was also inhibited by the hexane extract (IC50 1.75 µg/ml), dihydronitidine (0.59 µg/ml) and heitziquinone (6.2 µg/ml). Water extracts of Z. heitzii bark contain only low levels of dihydronitidine and show modest anti-parasitic activity.

conclusionsThree compounds with anti-parasitic activity were identified in Z. heitzii bark extract. The alkaloid dihydronitidine is the most effective of these, accounting for the bulk of activity in both erythrocytic and transmission-blocking assays. These compounds may present good leads for development of novel anti-malarials and add to the understanding of the chemical basis of the anti-parasitic activity in these classes of natural product.

Indexed as

AntimalarialsBiological ProductsInhibitory Concentration 50Plasmodium bergheiPlasmodium falciparumZanthoxylumAntimalarialsBiological ProductsAnti-malarialBenzophenanthridine alkaloidDihydronitidineEthnobotanyMalariaOokineteRutaceaeTransmission blockingZanthoxylum heitzii

Identifiers

PMID27649682
PMCPMC5029023
OpenAlexW2522216451

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.