Evidence map›Paper›PMID 42703808›Full record

ArticleInternational journal of fertility & sterility2026

Melatonin Improves Sperm Quality in Asthenozoospermic Men by Preserving Acrosome Integrity, Reducing Inflammation, and Regulating Apoptosis-Related Genes and Proteins during Freeze-Thawing.

Zahra Azizi, Malek Soleimani Mehranjani, Seyed Mohammad Ali Shariatzadeh, Nazila Najdi, Atena Sadat Azimi

Abstract read
In one paragraph

Article in International journal of fertility & sterility, 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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2 · The registry

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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

5 authors.

Zahra AziziDepartment of Biology, Faculty of Science, Arak University, Arak, Iran.
Malek Soleimani MehranjaniDepartment of Biology, Faculty of Science, Arak University, Arak, Iran. Email: m-soleimani@araku.ac.ir.ORCID 0000-0003-4822-2617
Seyed Mohammad Ali ShariatzadehDepartment of Biology, Faculty of Science, Arak University, Arak, Iran.
Nazila NajdiDepartment of Obstetrics and Gynaecology, School of Medicine, Arak University of Medical Sciences, Arak, Iran.
Atena Sadat AzimiDepartment of Reproductive and Biology, Infertility Treatment Centre of Amir-Al-Momenin Hospital, Arak, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Sperm freeze-thaw is a crucial technique in assisted reproductive technologies (ART), but it induces oxidative stress in sperm. Melatonin, a powerful antioxidant, reduces oxidative stress by penetrating mitochondria and neutralising free radicals. However, its protective role in the sperm of asthenozoospermic men during freeze-thaw remains poorly understood. This study examines the in vitro effects of melatonin on sperm quality in asthenozoospermic men during the freeze-thaw process. Materials and Methods: In this experimental study, semen samples were collected from 30 asthenozoospermic men and divided into three groups: control group, freeze group, and freeze+melatonin (1 mM) group. Sperm parameters including mitochondrial membrane potential (MMP), plasma membrane integrity, acrosomal reaction, and DNA fragmentation were assessed. The levels of superoxide dismutase (SOD), glutathione peroxidase (GSH), total antioxidant capacity (TAC), malondialdehyde (MDA), reactive oxygen species (ROS), tumour necrosis factor-alpha (TNF-α), and interleukin-10 (IL-10) were estimated. Expressions of apoptosis-related genes and proteins, BAX and BCL-2, were also analysed. Results: There was a significant decrease (P=0.004) in sperm parameters, MMP, plasma membrane and acrosome integrity, TAC, GSH, SOD, IL-10 levels, and Bcl-2 expression in the freeze group compared to the control group. Conversely, MDA, ROS, TNF-α, DNA fragmentation, and BAX expression significantly increased (P=0.010). However, all these parameters showed significant improvements in the freeze+melatonin group compared to the freeze group (P=0.019). Conclusion: Melatonin may improve sperm quality during freeze-thaw by increasing antioxidant defence, reducing inflammation via TNF-α/IL-10 modulation, inhibition of apoptosis through BAX/BCL-2 regulation, and preservation of acrosome integrity. These findings suggest that melatonin may have potential as a cryoprotectant in ART.

Indexed as

ApoptosisAsthenozoospermiaInflammatory CytokinesMelatoninOxidative Stress

Identifiers

PMID42703808
PMCPMC13535275

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