Evidence map›Paper›PMID 40641745›Full record

ArticleBiochemistry and biophysics reports2025

Prophylactic role of omega 3 fatty acids in bisphenol F-induced sexual and erectile dysfunction is associated with penile redox homeostasis.

Adeyemi Fatai Odetayo, Moses Agbomhere Hamed, Grace Edet Bassey, Oluranti Olayinka Titiloye, Samson Daniel Maduabuchi, Kazeem Bidemi Okesina, Luqman Aribidesi Olayaki

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Article in Biochemistry and biophysics reports, 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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Adeyemi Fatai OdetayoDepartment of Physiology, Faculty of Basic Medical Sciences, Federal University of Health Sciences, Ila-Orangun, Nigeria.
Moses Agbomhere HamedDepartment of Medical Laboratory Science, Afe Babalola University, Ado-Ekiti, Nigeria.
Grace Edet BasseyPhysiology Department, Faculty of Basic Medical Sciences, University of Uyo, Uyo, Nigeria.
Oluranti Olayinka TitiloyeDepartment of Anatomy and Cell Biology, Obafemi Awolowo University, Ife, Nigeria.
Samson Daniel MaduabuchiDepartment of Medical Laboratory Sciences, Leeds City University, Ibadan, Nigeria.
Kazeem Bidemi OkesinaDepartment of Physiology, University of Rwanda, Kigali, Rwanda.
Luqman Aribidesi OlayakiDepartment of Physiology, University of Ilorin, Ilorin, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Bisphenol F (BPF) is an established environmental pollutant that has been shown to distort erectile function. However, the effect of BPF on penile redox homeostasis is not known. On the other hand, omega-3 fatty acids (O3FA) are known antioxidants with fertility-enhancing properties. Despite these abilities, the ameliorative effect of O3FA on BPF-induced penile redox imbalance is unknown. Hence, this study was designed to add to the existing body of knowledge by investigating the role of penile redox homeostasis on BPF-induced erectile dysfunction and the possible ameliorative effect of O3FA. Methodology: Twenty male Wistar rats were randomly divided into four groups (n = 5/group) after two weeks acclimatization period as follows: control group (.5 ml of corn oil), O3FA group (300mg/kg of O3FA), BPF group (30mg/kg of BPF), and the BPF + O3FA group (30 mg/kg of BPF + 300mg/kg of O3FA). Results: BPF exposure led to sexual and erectile dysfunction, which was accompanied by a disruption in erectogenic enzymatic activities and circulatory testosterone. These events were accompanied by the down-regulation of penile NO/cGMP signaling, oxido-inflammatory response, and penile histoarchitecture distortion. These observed BPF-induced distortions were ameliorated in animals that received O3FA co-treatment with BPF. Conclusion: BPF-induced erectile dysfunction was associated with penile redox imbalance, and O3FA ameliorated BPF-induced penile toxicity.

Indexed as

Bisphenol FEndocrine disruptorNitric oxide (NO)/Cyclic guanosine monophosphate (cGMP)Penile erectionPenile redox imbalanceXanthine oxidase/uric acid signaling

Identifiers

PMID40641745
PMCPMC12242445

What Socratic holds

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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 Socratic graph.