Evidence map›Paper›PMID 42807300›Full record

ArticleInternational journal of medical sciences2026

Metformin-Functionalized Selenium Nanoparticles Restore Insulin Signaling and Metabolic Homeostasis in Letrozole-Induced Polycystic Ovary Syndrome Rat Model.

Uğur Ermis, Damla Binentoglu, Erdem Toktay, Huseyin Fatih Gul, Hasan Ilhan, Muhammed Yayla

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Article in International journal of medical sciences, 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

What it found

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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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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.

Uğur ErmisDepartment of Pharmacology; Faculty of Medicine; Kafkas University, 36100 Kars/Turkey.
Damla BinentogluDepartment of Pharmacology; Faculty of Medicine; Kafkas University, 36100 Kars/Turkey.
Erdem ToktayDepartment of Histology and Embryology; Faculty of Medicine; Kafkas University, 36100 Kars/Turkey.
Huseyin Fatih GulDepartment of Biochemistry; Faculty of Medicine; Kafkas University, 36100 Kars/Turkey.
Hasan IlhanDepartment of Biotechnology; Biotechnology Institute; Ankara University, 06100 Ankara/Turkey.
Muhammed YaylaDepartment of Pharmacology; Faculty of Medicine; Selcuk University, 42100 Konya/Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we designed a novel 'metformin-coated nanoselenium nanocomposite' (Met+SeNP) to leverage the synergistic potential of both agents delivered via a single nanoplatform, aiming to restore metabolic and hormonal homeostasis in a letrozole-induced PCOS rat model. Met+SeNP was synthesized via a redox reaction of sodium selenite and ascorbic acid in the presence of metformin, creating a stable metformin-functionalized selenium nanocomposite. The particles were characterized using UV-Vis spectroscopy, SEM, and EDX. Female Sprague-Dawley rats were divided into five groups: Healthy, PCOS (letrozole-induced), Metformin (300 mg/kg), SeNP (0.4 mg/kg), and Met+SeNP (nanocomposite dose, SeNP 0.4 mg/kg + Metformin 300 mg/kg). The nanocomposite treatment most effectively minimized weight gain (39.36% vs. PCOS controls), normalized HOMA-IR, and restored circulating LH, estrogen, and testosterone levels. Histopathological evaluation demonstrated a marked reduction in cystic follicles and recovery of corpus luteum formation following Met+SeNP therapy. Immunohistochemical analysis further revealed that Met+SeNP robustly reversed PCOS-induced suppression of INR, IRS-1, and IRS-2 expression in both liver and skeletal muscle tissues. In addition, the nanocomposite significantly improved serum ALT, AST, and ALP levels while maintaining normal urea and creatinine concentrations, supporting hepatic protection and systemic safety. The metformin-functionalized SeNP nanocomposite represents a promising potent therapeutic strategy for PCOS-associated metabolic dysfunction, outperforming monotherapies in restoring insulin signaling, endocrine balance, and tissue integrity.

Indexed as

MetforminPolycystic Ovary SyndromeSeleniumAnimalsDisease Models, AnimalFemaleHomeostasisHumansHypoglycemic AgentsInsulinInsulin ResistanceLetrozoleNanocompositesNanoparticlesRatsRats, Sprague-DawleyHypoglycemic AgentsInsulinLetrozoleMetforminSeleniuminsulin resistancemetforminnanomedicinenanoseleniumrat

Identifiers

PMID42807300
PMCPMC13617503

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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.