Evidence map›Paper›PMID 41684535›Full record

ArticleToxicology reports2026

Berberine nanoemulsion against nephrotoxicity induced by bisphenol a in rats during pre-puberty stage.

Shahnaz Rajabi, Atena Mansouri, Tahora Fakhrtaha, Parisa Sadighara, Fariborz Samini, Saeed Samarghandian, Tahereh Farkhondeh

Abstract read
In one paragraph

Article in Toxicology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Shahnaz RajabiMedical Toxicology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Atena MansouriCellular and Molecular Research Center, Birjand University of Medical Sciences, Birjand, Iran.
Tahora FakhrtahaDepartment of pathology, Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Iran.
Parisa SadigharaDepartment of Environmental Health Engineering, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Fariborz SaminiNeuroscience Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Saeed SamarghandianDepartment of Medical Physiology, School of Medicine, Neyshabur University of Medical Sciences, Neyshabur, Iran.
Tahereh FarkhondehGeriatric Health Research Center, Birjand University of Medical Sciences, Birjand, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study evaluated the effects of berberine nanoemulsion (BNE) against nephrotoxicity induced by bisphenol A (BPA), a plastic chemical, in rats during the pre-puberty stage. Thirty-six male Wistar rats (23-day-old) were randomly allocated to six groups (n = 6): Group 1 (Control). Group 2 (BPA): BPA (200 mg/kg) and saline. Groups 3 (BNE 5) and 4 (BNE 10): BNE (5 and 10 mg/kg,). Groups 5 (BPA + BNE 5) and 6 (BPA + BNE 10): BPA with BNE (5 and 10 mg/kg). After 30 days, kidney samples were obtained for histopathological and biochemical tests. BPA increased serum urea, uric acid, creatinine (Cr), blood urea nitrogen (BUN), and kidney levels of malondialdehyde (MDA), nitric oxide (NO), interleukin-6 (IL-6), interleukin-1β (IL-1β), and tumor necrosis factor-α (TNF-α) versus controls. BPA decreased estimated glomerular filtration rate (eGFR), reduced glutathione (GSH), and superoxide dismutase (SOD) activity. BNE (10 mg/kg) reversed these changes to near-control levels. Histopathology showed lumen obliteration of renal tubules, dilated vessels, glomerular atrophy, and large capsular space in the BPA group. Less inflammation and improved glomerular architecture were seen in the BPA + BNE10 group. In conclusion, BNE (10 mg/kg) significantly alleviated BPA-induced oxidative stress, inflammation and histopathological changes in the kidney of rats during the pre-puberty stage due to its antioxidant and anti-inflammatory effects. This finding confirms the safety and efficacy of BNE in nephrotoxic model during pre-puberty stage. It can be suggested to investigate this agent in clinical study as a possible therapeutic approach.

Indexed as

Berberine nanoemulsionBisphenolNephrotoxicityPre-pubertyRat

Identifiers

PMID41684535
PMCPMC12891865

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