Evidence map›Paper›PMID 42766218›Full record

ArticleJournal of molecular histology2026

Propolis ameliorates cisplatin-induced nephrotoxicity via activation of Nrf2/HO-1 signaling pathway in rats.

Alyah Fallatah, Alaa Essam, Abd El-Fattah B M El-Beltagy, Amr M Abdelghany, Neven A Salah

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Article in Journal of molecular histology, 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

5 authors.

Alyah FallatahDepartment of Chemistry, Faculty of Science, Mansoura University, Mansoura, 35516, Egypt.
Alaa EssamDepartment of Chemistry, Faculty of Science, Mansoura University, Mansoura, 35516, Egypt. aalaaessam38@gmail.com.
Abd El-Fattah B M El-BeltagyZoology Department, Faculty of Science, Damanhour University, Damanhour, Egypt.
Amr M AbdelghanySpectroscopy Department, Physics Division, National Research Center, 33 Elbehouth St, Dokki, Cairo, 12311, Egypt.
Neven A SalahDepartment of Chemistry, Faculty of Science, Mansoura University, Mansoura, 35516, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cisplatin is among the most widely used chemotherapeutic drugs for the treatment of solid tumors; nonetheless, nephrotoxicity persists as a significant dose-limiting adverse effect. The current study focuses on the protective effect of propolis against cisplatin-induced kidney damage in experimental rats. Nephrotoxicity was induced by a single intraperitoneal injection of cisplatin at a dose of 5 mg/kg, ip, followed by propolis oral administration. The chemical profile of the propolis extract was characterized using liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS). Biochemical parameters of renal function (urea and creatinine), oxidative stress markers (MDA, SOD, CAT and GSH), proinflammatory markers (IL-6, TNF-α and IL-1ꞵ) and RT-PCR were performed along with histopathological and immunohistochemical investigations. LC-MS analysis revealed that the propolis contained several bioactive phenolic acids and flavonoids, with pyrocatechol, iso-ferulic acid, gallic acid, apigenin, kaempferol, quercetin, which may contribute to the antioxidant and nephroprotective effects of propolis. The results demonstrated that cisplatin markedly increased serum levels of urea and creatinine and elevated lipid peroxidation and inflammation, accompanied by notable damage in renal structure. Conversely, propolis treatment significantly ameliorated these adverse effects by restoring antioxidant status, reducing oxidative stress and improving histological structure. Furthermore, administration of propolis significantly suppressed inflammation by reducing proinflammatory cytokines levels and the expression of caspase-3. In addition, immunohistochemical results revealed that propolis treatment markedly increased Nrf2/HO-1 expression in kidney tissue. In conclusion, these findings suggested that propolis exerts nephroprotective effects against cisplatin-induced nephrotoxicity via its anti-inflammatory and antioxidant activities.

Indexed as

CisplatinHeme Oxygenase-1KidneyKidney DiseasesNF-E2-Related Factor 2PropolisSignal TransductionAnimalsAntioxidantsMaleOxidative StressRatsAntioxidantsCisplatinHeme Oxygenase-1NF-E2-Related Factor 2PropolisAntioxidantCisplatinNephrotoxicityNrf2/HO-1Propolis

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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.