Evidence map›Paper›PMID 41710801›Full record

ArticleJournal of parasitology research2026

Potentiality of LPS in Ameliorating the Histopathological Responses in Visceral Leishmaniasis-Infected Mice.

Ghusoon A A Al-Maphregy, Hazima Mossa Alabassi, Ashwaq Ahmed Hussein

Abstract read
In one paragraph

Article in Journal of parasitology research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

3 authors.

Ghusoon A A Al-MaphregyDepartment of Biology, College of Education for Pure Sciences/Ibn Al-Haitham, University of Baghdad, Baghdad, Iraq, uobaghdad.edu.iq.ORCID https://orcid.org/0000-0001-8169-6262
Hazima Mossa AlabassiDepartment of Biology, College of Education for Pure Sciences/Ibn Al-Haitham, University of Baghdad, Baghdad, Iraq, uobaghdad.edu.iq.ORCID https://orcid.org/0000-0002-9218-8762
Ashwaq Ahmed HusseinDepartment of Biology, College of Education for Pure Sciences/Ibn Al-Haitham, University of Baghdad, Baghdad, Iraq, uobaghdad.edu.iq.ORCID https://orcid.org/0000-0002-9536-4127

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Visceral leishmaniasis is the second most fatal parasite illness worldwide, and it is the most severe type of leishmaniasis. LPS is a crucial chemical compound on the bacterial cell wall that the host recognizes and uses to launch an immune response to eliminate invasive infections. Materials and Methods: Four concentrations of LPS were used to treat infected mice with visceral leishmaniasis (20, 40, 60, and 80 ng/mL). Differential cell count and phagocytic index tests were done, then the liver and spleen were separated, and a histopathological assay was performed. Results: The findings demonstrated that all blood cells, with the exception of basophils, varied significantly between the uninfected and infected groups. With the exception of the 40 ng/mL concentration, there were notable variations in lymphocytes between the treated and infected groups as well as across the treated groups. With the exception of the 60 ng/mL concentration, neutrophils and monocytes showed significant changes between the treated and infected groups. Eosinophils, however, showed noticeable differences between the infected group and the treated groups. As for the phagocytic index, there was a significant difference between the uninfected and treated groups with the infected group. Histopathological results showed the effectiveness of LPS in the treatment of infected liver and spleen, especially in low concentrations (20, 40, and 60 ng/mL), whereas the highest concentration of LPS showed significant damage to liver and spleen tissue. Conclusion: This result opens up prospects for the possibility of using LPS as a treatment for many pathogens.

Indexed as

leishmaniasisLPSvisceral leishmaniasis

Identifiers

PMID41710801
PMCPMC12910174

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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.