Evidence map›Paper›PMID 41428725›Full record

ArticleJBRA assisted reproduction2026

Zingerone Mitigates Testicular Dysfunction Induced by Cisplatin.

Elham Younesi, Layasadat Khorsandi, Amirhesam Keshavarz Zarjani, Abbas Heidari-Moghadam, Mohammad Javad Khodayar, Yousef Asadi-Fard

Abstract read
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Article in JBRA assisted reproduction, 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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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Elham YounesiStudent Research committee, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Layasadat KhorsandiCellular and Molecular Research Center, Medical Basic Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Amirhesam Keshavarz ZarjaniDepartment of Anatomical Sciences, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Abbas Heidari-MoghadamDepartment of Anatomical Sciences, School of Medicine, Dezful University of Medical Sciences, Dezful, Iran.
Mohammad Javad KhodayarToxicology Research Center, Medical Basic Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Yousef Asadi-FardDepartment of Anatomy, School of Medicine, Arak University of Medical Sciences, Arak, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCisplatin is one of the most widely used antitumor drugs globally, particularly in treating various solid tumors. The reproductive system is impacted by cisplatin toxic effects. This study aims to understand how Zingerone affects spermatogenesis defects in mice.

methodsIn the present experimental laboratory study, the 48 male NMRI mice (6 to 8 weeks of age, 25 to 30g weight) were treated with Cisplatin (7 mg/kg) for 5 days and zingerone for 30 days at concentrations of 10, 20, and 40 mg/kg before cisplatin administration. After the treatment period, the testicles were dissected immediately following sacrifice. Morphometric parameters, serum testosterone concentration, histology, Bax/Bcl-2 ratio, and testis weight have been assessed. To determine levels of oxidative stress, malondialdehyde contents and antioxidant levels were evaluated.

resultsCisplatin-induced structural damages enhanced the Bax/Bcl-2 ratio, and reduced testosterone levels and testis weight. Cisplatin caused oxidative stress by enhancing malondialdehyde contents in the mouse testicles. Zingerone dose-dependently reduced the Bax/Bcl-2 ratio and reversed the histological changes, testosterone levels, and antioxidant capacity.

conclusionsAccording to the results of the present study, Pretreatment with zingerone can improve testosterone production by preventing apoptosis and oxidative stress in the testicles of mice that have undergone cisplatin intoxication.

Indexed as

Antineoplastic AgentsCisplatinGuaiacolTesticular DiseasesTestisAnimalsAntioxidantsMaleMalondialdehydeMiceOxidative StressSpermatogenesisTestosteroneAntineoplastic AgentsAntioxidantsCisplatinGuaiacolMalondialdehydeTestosteronezingeroneapoptosiscisplatinoxidative stressreproductive systemzingerone

Identifiers

PMID41428725
PMCPMC13059646

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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.