Evidence map›Paper›PMID 39225734›Full record

ArticleActa parasitologica2024

Zingiber officinale Ameliorates Acute Toxoplasmosis-Induced Pathology in Mice.

Asmaa M El-Kady, Hayam Elshazly, Muslimah N Alsulami, Haleema H Albohiri, Eman Abdullah Alshehri, Mashael S Alfaifi, Khalil Mohamed, Majed H Wakid, Hattan S Gattan, Sarah A Altwaim and 5 more

Abstract read
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Article in Acta parasitologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

3 citing papers in PubMed.

  1. Article
  2. Seroprevalence ofOne health (Amsterdam, Netherlands) · 2025
    Article
  3. 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

15 authors.

Asmaa M El-KadyDepartment of Medical Parasitology, Faculty of Medicine, South Valley University, Qena, 83523, Egypt. asmaa.elkady@med.svu.edu.eg.ORCID http://orcid.org/0000-0002-9294-2630
Hayam ElshazlyDepartment of Biology, Faculty of Sciences-Scientific Departments, Qassim University, Bu-raidah, Qassim, 52571, Saudi Arabia.
Muslimah N AlsulamiDepartment of Biology, College of Science, University of Jeddah, Jeddah, Saudi Arabia.ORCID http://orcid.org/0000-0002-0447-8963
Haleema H AlbohiriDepartment of Biology, College of Science, University of Jeddah, Jeddah, Saudi Arabia.ORCID http://orcid.org/0009-0005-8974-8238
Eman Abdullah AlshehriDepartment of Zoology, College of Science, King Saud University, Riyadh, 11362, Saudi Arabia.
Mashael S AlfaifiDepartment of Epidemiology and Medical Statistics, Faculty of Public Health and Health Informatics, Umm Al-Qura 21 University, Mecca, 21961, Saudi Arabia.
Khalil MohamedDepartment of Epidemiology and Medical Statistics, Faculty of Public Health and Health Informatics, Umm Al-Qura 21 University, Mecca, 21961, Saudi Arabia.
Majed H WakidDepartment of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, 21589, Saudi Arabia. mwakid@kau.edu.sa.ORCID http://orcid.org/0000-0003-4941-5373
Hattan S GattanDepartment of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, 21589, Saudi Arabia.ORCID http://orcid.org/0000-0003-3514-4912
Sarah A AltwaimSpecial Infectious Agents unit, King Fahd Medical Research Center, Jeddah, 21589, Saudi Arabia.
Wafa Abdullah I Al-MegrinDepartment of Biology, College of Science, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia.
Ghaliah H AlmalkiDepartment of Biology, College of Science, Jazan University, Jazan, 45142, Saudi Arabia.
Iman A M Abdel-RahmanDepartment of Pharmacognosy, Faculty of Pharmacy, South Valley University, Qena, 83523, Egypt.
Hatem A ElshabrawyDepartment of Molecular and Cellular Biology, College of Osteopathic Medicine, Sam Houston State University, Conroe, TX, 77304, USA. hatem.elshabrawy@shsu.edu.
Salwa YounisDepartment of Medical Parasitology, Faculty of Medicine, Alexandria University, Alexandria, 21526, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundToxoplasma gondii (T. gondii) infects one third of the world's population with significant illness, mainly among immunocompromised individuals and pregnant women. Treatment options for toxoplasmosis are limited which signifies the need for novel, potent, and safe therapeutic options. The goal of this study was to assess the effectiveness of the ethanolic extract of Zingiber officinale (Z. officinale) in treating mice infected with the RH T. gondii strain. MATERIALS AND

methodsGas Chromatography/Mass Spectrometry (GC/MS) was used to identify components of ethanolic extract of Z. officinale. A total of 80 mice were randomly allocated into four experimental groups that contained 20 mice each. The first group was left uninfected (uninfected control), while three groups were infected with T. gondii RH virulent strain tachyzoites at 2500 tachyzoites/mouse. One infected group was left untreated (infected, untreated), whereas the other two groups were treated orally with either spiramycin (positive control) or Z. officinale ethanolic extract at doses of 200 mg/kg and 500 mg/kg, respectively for 5 days, starting the day of infection. Ten mice from each group were used to assess mice survival in different groups, whereas the other ten mice in each group were sacrificed on the 5th day post-infectin (dpi) to estimate the treatment efficacy by quantifying liver parasite load, liver function, nitric oxide (NO) production, and levels of antioxidant enzymes. Additionally, histopathological studies were performed to evaluate the therapeutic effect of Z. officinale treatment on toxoplasmosis-induced pathological alterations in liver, brain, and spleen.

resultsTreatment with Z. officinale ethanolic extract extended the survival of mice till 9th dpi compared to 7th dpi in infected untreated mice. Higher percentage of mice survived in Z. officinale-treated group compared to spiramycin-treatment group at different time points. Liver parasite loads were significantly lower in Z. officinale extract-treated mice and spiramycin-treated mice compared to infected untreated mice which correlated with significantly lower levels of serum liver enzymes (ALT, AST) and nitric oxide (NO), as well as significantly higher catalase (CAT) antioxidant enzyme activity. Scanning electron microscopy (SEM) examination of tachyzoites from the peritoneal fluid revealed marked damage in tachyzoites from Z. officinale-treated group compared to that from infected untreated mice. Moreover, treatment with Z. officinale ethanolic extract alleviated infection-induced pathological alterations and restored normal tissue morphology of liver, brain, and spleen.

conclusionOur results demonstrated that Z. officinale treatment reduced parasite burden and reversed histopathological and biochemical alterations in acute murine toxoplasmosis. These findings support the potential utility of Z. officinale as a future effective natural therapeutic for toxoplasmosis. Further studies are needed to determine the effective active ingredient in Z. officinale extract that can be further optimized for treatment of toxoplasmosis.

Indexed as

Plant ExtractsToxoplasmaZingiber officinaleAnimalsBrainDisease Models, AnimalFemaleGas Chromatography-Mass SpectrometryLiverMiceSpleenToxoplasmosisToxoplasmosis, AnimalPlant ExtractsBrainLiverParasiteSpiramycinSpleenTachyzoitesToxoplasma gondiiToxoplasmosisZingiber officinale

Identifiers

PMID39225734

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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.