Evidence map›Paper›PMID 40889041›Full record

ArticleBiological trace element research2026

Bismuth Oxide Nanoparticles-Induced Subclinical Nephrotoxicity in Male Mice: Role of Oxidative Stress and Apoptosis.

Mohadese Farahani, Shahrbanoo Shahmohammadi, Ali Golshokooh, Mohammad Nouri, Hasti Okhovatiyan, Fatemeh Farahani, Maryam Hadad Dehshiri, Mobina JamalAbbasi, Amir Jalali

Abstract read
PubMed Publisher
In one paragraph

Article in Biological trace element 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

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

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

9 authors.

Mohadese FarahaniDepartment of Biology, Faculty of Science, Arak University, Arak, 3848177584, Iran.
Shahrbanoo ShahmohammadiDepartment of Biology, Faculty of Science, Arak University, Arak, 3848177584, Iran.
Ali GolshokoohDepartment of Biology, Faculty of Science, Arak University, Arak, 3848177584, Iran.
Mohammad NouriDepartment of Biology, Faculty of Science, Arak University, Arak, 3848177584, Iran.
Hasti OkhovatiyanDepartment of Biology, Faculty of Science, Arak University, Arak, 3848177584, Iran.
Fatemeh FarahaniDepartment of Biology, Faculty of Science, Arak University, Arak, 3848177584, Iran.
Maryam Hadad DehshiriDepartment of Biology, Faculty of Science, Arak University, Arak, 3848177584, Iran.
Mobina JamalAbbasiDepartment of Biology, Faculty of Science, Arak University, Arak, 3848177584, Iran.
Amir JalaliDepartment of Biology, Faculty of Science, Arak University, Arak, 3848177584, Iran. a-jalali@araku.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bismuth's unique properties have led to its widespread use in medical, cosmetic, and electronic applications. However, increasing evidence suggests potential toxicity, particularly from nanoparticle forms that may accumulate in organs. This study investigated the nephrotoxic effects of bismuth oxide nanoparticles (Bi₂O₃ NPs) in male NMRI mice, focusing on underlying molecular mechanisms. Adult mice were divided into control and experimental groups receiving 25-800 mg/kg Bi₂O₃ NPs via oral gavage for 30 days. Kidney function was assessed through serum urea and creatinine measurements. Gene expression analysis evaluated apoptosis markers (Bcl2, Bax, Casp3) and oxidative stress pathways (Nrf2, Hmox1) using RT-PCR. Histopathological examination assessed renal tissue alterations. Results revealed no significant changes in serum urea or creatinine levels. Molecular analysis revealed significant gene alterations: Bax (5.969-fold, p = 0.008) and Casp3 (5.568-fold, p = 0.007) upregulation, alongside Bcl2 downregulation (0.239-fold, p = 0.039), indicating apoptosis. Nrf2 (9.569-fold, p = 0.002) and Hmox1 (4.993-fold, p = 0.039) induction confirmed oxidative stress. Data demonstrate Bi₂O₃ NPs trigger apoptosis and oxidative stress. Histological examination revealed glomerular volume increased to 4.79 ± 0.22 mm

Indexed as

ApoptosisBismuthKidneyKidney DiseasesMetal NanoparticlesNanoparticlesOxidative StressAnimalsHeme Oxygenase-1MaleMembrane ProteinsMiceNF-E2-Related Factor 2Bismuthbismuth oxideHeme Oxygenase-1Hmox1 protein, mouseMembrane ProteinsNF-E2-Related Factor 2Apoptosis pathwaysBismuth oxide nanoparticlesGene expressionOxidative stressSubclinical nephrotoxicity

Identifiers

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.