Evidence map›Paper›PMID 41952867›Full record

ArticleInternational journal of reproductive biomedicine2026

Ivermectin mitigates 7,12-dimethylbenz(a) anthracene-induced reproductive toxicity in female wistar rats: An experimental study.

Ali Jebeli Eshrat Abadi, Fatemeh Zahra Gharib, Seyed Mohammad Hosseini

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Article in International journal of reproductive biomedicine, 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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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

3 authors.

Ali Jebeli Eshrat AbadiDepartment of Pathology, Bab.C., Islamic Azad University, Babol, Iran.
Fatemeh Zahra GharibDepartment of Clinical Sciences, Bab.C., Islamic Azad University, Babol, Iran.
Seyed Mohammad HosseiniDepartment of Pathology, Bab.C., Islamic Azad University, Babol, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: 7,12-dimethylbenz(a)anthracene (DMBA) is a pervasive environmental polycyclic aromatic hydrocarbon that exerts genotoxic and endocrine-disrupting effects in female reproductive tissues, largely through oxidative stress and induction of apoptosis. Ivermectin, a food and drug administration-approved antiparasitic agent, has emerging anti-inflammatory and antioxidant properties. Objective: We evaluated whether Ivermectin could protect the ovarian and uterine tissues against DMBA-induced injury. Materials and Methods: In this experimental study, 20 female Wistar rats (8 wk, 210 Results: Our findings showed that DMBA induced significant oxidative stress and tissue damage, along with hormone disruption and upregulation of pro-apoptotic genes. In contrast, Ivermectin co-treatment largely reversed these changes, such as reducing the serum malondialdehyde and increasing superoxide dismutase and total antioxidant capacity. Moreover, the hormone level balance significantly shifted toward control values. Histopathological examination showed DMBA-induced ovarian damage and uterine epithelial degeneration, which were attenuated by Ivermectin. Conclusion: Ivermectin significantly ameliorated DMBA-induced oxidative damage, endocrine disruption, and apoptotic signaling in female rats. These findings suggest Ivermectin's potential for protecting the reproductive tissues from environmental toxin injury.

Indexed as

DMBAIvermectinRat.Reproductive health

Identifiers

PMID41952867
PMCPMC13054294

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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.