Evidence map›Paper›PMID 41287470›Full record

ArticleIranian biomedical journal2025

Reno-Protective Properties of Azolla pinnata Extract Against Gentamicin-Induced Kidney Damage Are Attributed to Its Antioxidant Effects.

Mohammad Ghanbari Alamoti, Farideh Jalali Mashayekhi, Naser Hosseini, Houshang Najafi, Saeed Changizi-Ashtiyani

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Article in Iranian biomedical journal, 2025. 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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5 · Who and what money

Authors and funding

5 authors.

Mohammad Ghanbari AlamotiDepartment of Physiology, School of Medicine, Arak University of Medical Sciences, Arak, Iran.
Farideh Jalali MashayekhiDepartment of Biochemistry and Genetics, School of Medicine, Arak University of Medical Sciences, Arak, Iran.
Naser HosseiniDepartment of Medicinal Plants, Faculty of Agriculture and Natural Resources, Arak University, Arak, Iran.
Houshang NajafiDepartment of Physiology, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Saeed Changizi-AshtiyaniDepartment of Physiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gentamicin, a powerful aminoglycoside antibiotic, is limited in clinical use due to dose-related kidney toxicity, mainly caused by oxidative stress. A. pinnata, an antioxidant-rich aquatic fern, has not been extensively studied for renoprotection against GM-induced kidney damage. This research assessed the protective effects of a hydroalcoholic extract of A. pinnata on GM nephrotoxicity. Methods: Forty male Wistar rats were divided into five groups (n = 8): control, sham, GM (100 mg/kg/day, i.p.), and GM plus A. pinnata extract (10 or 20 mg/kg/day, orally). After seven days, renal function markers (serum creatinine and urea), oxidative stress parameters (MDA, FRAP, CAT, and GPX), TNF-α, and renal histopathology were assessed. Results: GM significantly damaged kidney function and induced oxidative stress, as shown by increased levels of creatinine, urea, and MDA, along with reduced FRAP and CAT activity (p < 0.05). Co-treatment with A. pinnata extract, especially at 20 mg/kg, significantly lessened these effects by restoring kidney function markers, boosting antioxidant defenses, and lowering lipid peroxidation. The extract did not have a significant impact on either GPX activity or TNF-α levels. Histopathological analysis revealed that GM-induced tubular necrosis and glomerular damage were significantly ameliorated by A. pinnata in a dose-dependent manner. Conclusion: A. pinnata extract offers notable protection against kidney damage caused by gentamicin, mainly by enhancing the body's natural antioxidant defenses, decreasing lipid peroxidation, and maintaining the normal structure of kidney tissue. These findings suggest that A. pinnata could serve as a valuable complementary treatment to improve the safety of GM use.

Indexed as

AntioxidantsFernsGentamicinsKidneyKidney DiseasesPlant ExtractsAnimalsCatalaseCreatinineLipid PeroxidationMaleOxidative StressRatsRats, WistarUreaAntioxidantsCatalaseCreatinineGentamicinsPlant ExtractsUreaGentamicinsKidney failureOxidative stress

Identifiers

PMID41287470
PMCPMC13310546

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