Evidence map›Paper›PMID 40292055›Full record

ArticleArchives of Razi Institute2024

Kidney Toxicity Studies in Mice (BALB/C) Recurrently Infected with

D Audu, O A Idowu, F M Mshelbwala, A B Idowu

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Archives of Razi Institute, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

D AuduDepartment of Pure and Applied Zoology, College of Biosciences, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria.
O A IdowuDepartment of Pure and Applied Zoology, College of Biosciences, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria.
F M MshelbwalaDepartment of Veterinary Pathology, College of Veterinary Medicine, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria.
A B IdowuDepartment of Pure and Applied Zoology, College of Biosciences, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Individuals residing in regions where malaria is endemic are frequently exposed to the disease and subsequently treated. The frequent exposure to malaria and its treatment could exert a deleterious effect on the kidneys, which are responsible for eliminating metabolites. This could potentially lead to oxidative stress and impair their function. Therefore, this study aimed to investigate the potential consequences of repeated exposure to malaria parasites and treatment with artemether plus lumefantrine (AL) or artesunate plus amodiaquine (AA) on kidney oxidative stress and functional markers. Three groups of male mice were randomly assigned for the study: the control group was administered distilled water, while the other two groups were infected with berghei

Indexed as

AmodiaquineAntimalarialsArtemisininsEthanolaminesFluorenesKidneyMalariaPlasmodium bergheiAnimalsArtemetherArtemether, Lumefantrine Drug CombinationArtesunateDrug CombinationsLumefantrineMaleMiceAmodiaquineamodiaquine, artesunate drug combinationAntimalarialsArtemetherArtemether, Lumefantrine Drug CombinationArtemisininsArtesunateDrug CombinationsEthanolaminesFluorenesLumefantrineAntimalarial DrugsKidneyMalariaOxidative StressRenal FunctionRepeated Exposure

Identifiers

PMID40292055
PMCPMC12018744

What OpenQuestion holds

Textmetadata
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.