Evidence map›Paper›PMID 41896927›Full record

ArticleBMC pharmacology & toxicology2026

Toxicological evaluation of paracetamol and ibuprofen: genetic and hematological alterations in male albino mice.

Shimaa M Elgingihy, Ayaat M Elmaghraby, Yehia A Mustafa, Mohamed A Elseehy, Amany S Haggag, Salah M Abdel-Rahman

Abstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Shimaa M ElgingihyDepartment of Genetics, Faculty of Agriculture, Alexandria University, Alexandria, Egypt. igsr.ShimaaElgingihy@alexu.edu.eg.
Ayaat M ElmaghrabyDepartment of Nucleic Acid Research, Genetic Engineering and Biotechnology Research Institute (GEBRI), City of Scientific Research and Technological Applications (SRTA-City), Alexandria, Egypt.
Yehia A MustafaDepartment of Genetics, Faculty of Agriculture, Alexandria University, Alexandria, Egypt.
Mohamed A ElseehyDepartment of Genetics, Faculty of Agriculture, Alexandria University, Alexandria, Egypt.
Amany S HaggagDepartment of Nucleic Acid Research, Genetic Engineering and Biotechnology Research Institute (GEBRI), City of Scientific Research and Technological Applications (SRTA-City), Alexandria, Egypt.
Salah M Abdel-RahmanDepartment of Nucleic Acid Research, Genetic Engineering and Biotechnology Research Institute (GEBRI), City of Scientific Research and Technological Applications (SRTA-City), Alexandria, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antipyretic drugs are widely used to manage fever and pain and are generally regarded as safe when administered within recommended therapeutic ranges. Nevertheless, concerns remain regarding the potential biological effects associated with repeated or sub-chronic exposure. The present study evaluated the hematological, histopathological, and molecular effects of two commonly used antipyretics, paracetamol and ibuprofen, following repeated administration in male albino mice. Hematological analysis revealed drug-related alterations in selected blood parameters, with more pronounced changes observed in ibuprofen-treated groups, while paracetamol exposure was associated with comparatively milder effects. Qualitative histopathological examination demonstrated organ-specific structural alterations in the testes, liver, kidneys, and stomach, which were generally mild in nature and more frequently observed at higher experimental dose levels. No evidence of overt testicular failure or severe tissue damage was detected within the exposure period. At the molecular level, repeated exposure to paracetamol and ibuprofen was associated with downregulation of TNF-α and connexin 43 mRNA expression in peripheral blood, suggesting early systemic transcriptional responses accompanying the observed histological changes. However, molecular findings were limited to mRNA expression analysis and did not include protein-level or tissue-specific validation. Overall, the results indicate that repeated sub-chronic exposure to paracetamol and ibuprofen at therapeutic-equivalent dose ranges may be associated with early hematological, histological, and molecular alterations in mice. These findings highlight the importance of cautious and rational use of widely prescribed antipyretic drugs and underscore the need for further studies to elucidate long-term safety, underlying mechanisms, and tissue-specific functional outcomes.

Indexed as

AcetaminophenAntipyreticsIbuprofenAnimalsConnexin 43KidneyLiverMaleMiceRNA, MessengerStomachTestisTumor Necrosis Factor-alphaAcetaminophenAntipyreticsConnexin 43IbuprofenRNA, MessengerTumor Necrosis Factor-alphaAlbino miceConnexin 43Drug-induced toxicityGene expressionHematologyHistopathologyIbuprofenParacetamolTNF-α

Identifiers

PMID41896927
PMCPMC13063668

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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.