Evidence map›Paper›PMID 25890324›Full record

ArticleMalaria journal2015

In vivo antiplasmodial and toxicological effect of Maytenus senegalensis traditionally used in the treatment of malaria in Tanzania.

Hamisi M Malebo, Victor Wiketye, Shaaban J Katani, Nteghenjwa A Kitufe, Vitus A Nyigo, Calister P Imeda, John W Ogondiek, Richard Sunguruma, Paulo P Mhame, Julius J Massaga and 5 more

Abstract 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 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–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

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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Isolation and Identification of Phytocompounds fromMolecules (Basel, Switzerland) · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Heliyon · 2021
    Article
  14. A Review on Phytochemicals of the GenusMolecules (Basel, Switzerland) · 2021
    Review
  15. Medicinal plants as a fight against murine blood-stage malaria.Saudi journal of biological sciences · 2021
    Review
  16. Antimalarial Plants Used across Kenyan Communities.Evidence-based complementary and alternative medicine : eCAM · 2020
    Review
  17. Exploring Antimalarial Herbal Plants across Communities in Uganda Based on Electronic Data.Evidence-based complementary and alternative medicine : eCAM · 2019
    Review
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

15 authors.

Hamisi M MaleboDepartment of Traditional Medicine Research, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. Malebo@hotmail.com.
Victor WiketyeNgongongare Medical Research Centre, P.O Box 514, Usa River, Arusha, Tanzania. wikeetye@yahoo.co.uk.
Shaaban J KataniDepartment of Traditional Medicine Research, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. katanisj@yahoo.co.uk.
Nteghenjwa A KitufeDepartment of Traditional Medicine Research, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. nkitufe@yahoo.com.
Vitus A NyigoDepartment of Traditional Medicine Research, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. nyigoo@yahoo.com.
Calister P ImedaDepartment of Traditional Medicine Research, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. cimeda@yahoo.com.
John W OgondiekNgongongare Medical Research Centre, P.O Box 514, Usa River, Arusha, Tanzania. jwilfredy@yahoo.com.
Richard SungurumaDepartment of Traditional Medicine Research, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. rsunguruma@yahoo.com.
Paulo P MhameTraditional Medicine Unit, Ministry of Health and Social Welfare, P.O. Box 9083, Dar es Salaam, Tanzania. pmhame@yahoo.com.
Julius J MassagaHeadquarters, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. jjmassaga@gmail.com.
Bertha MammuyaGovernment Chemist Laboratory Agency, P. O. Box 164, Dar es Salaam, Tanzania. mamuyab@yahoo.com.
Kesheni P SenkoroHeadquarters, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. ksenkoro@yahoo.com.
Susan F RumishaHeadquarters, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. srumisha@nimr.or.tz.
Mwelecele N MalecelaHeadquarters, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. mmalecela@hotmail.com.
Andrew Y KituaHeadquarters, National Institute for Medical Research, 3 Barack Obama Drive, P.O. Box 9653, 11101, Dar es Salaam, Tanzania. akitua@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn Tanzania and elsewhere, medicinal plants, including Maytenus senegalensis, are still widely used in the treatment of malaria and other ailments. The aim of the present study was to investigate the in vivo antiplasmodial and toxic effects in mice.

methodsOral antiplasmodial and acute toxicity of the ethanolic root extract of M. senegalensis was evaluated in mice. The Peters 4-day in vivo antiplasmodial effect against early rodent malaria infection in chloroquine-sensitive Plasmodium berghei NK 65 strain in mice.

resultsThe M. senegalensis extract was found non-toxic and the oral median lethal dose in mice was determined to be greater than 1,600 mg/kg body weight. The findings revealed a significant (P = 0.001) daily increase in the level of parasitaemia in the parasitized untreated groups and a significant (P < 0.001) dose dependent decrease in parasitaemia in the parasitized groups treated with varying doses ranging from 25 to 100 mg/kg body weight of M. senegalensis extract and the standard drug sulphadoxine/pyrimethamine at 25/1.25 mg/kg body weight. Overall, the dose dependent parasitaemia suppression effects were in the order of: 25/1.25 mg/kg body weight of sulphadoxine/pyrimethamine > 100 mg/kg > 75 mg/kg > 50 mg/kg > 25 mg/kg body weight of M. senegalensis extract.

conclusionThe implications of these findings is that M. senegalensis ethanolic root bark extract possess potent antiplasmodial effect and may, therefore, serve as potential sources of safe, effective and affordable anti-malarial drugs. The displayed high in vivo antiplasmodial activity and lack of toxic effect render M. senegalensis a candidate for the bioassay-guided isolation of compounds which could develop into new lead structures and candidates for drug development programmes against human malaria.

Indexed as

Administration, OralAnimalsAntimalarialsFemaleLethal Dose 50MalariaMaleMaytenusMiceParasitemiaPlant BarkPlant ExtractsPlant RootsPlants, MedicinalPlasmodium bergheiTanzaniaAntimalarialsPlant Extracts

Identifiers

PMID25890324
PMCPMC4446455

What OpenQuestion holds

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Registered trials

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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.