Evidence map›Paper›PMID 41942538›Full record

ArticleScientific reports2026

Effect of nanoliposomal gamma-oryzanol on cryosurvival, oxidative balance, and fertility of frozen-thawed ram spermatozoa.

Roughayeh Abbasi, Ramin Farhadi, Sara Ghaffarian Varjovi, Abouzar Najafi

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In one paragraph

Article in Scientific reports, 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

4 authors.

Roughayeh AbbasiDepartment of Biology, Faculty of Basic Sciences, Azarbaijan Shahid Madani University, Tabriz, Iran.
Ramin FarhadiDepartment of Animal Science, Faculty of Agriculture, University of Kurdistan, Sanandaj, Iran.
Sara Ghaffarian VarjoviDepartment of Biology, Faculty of Basic Sciences, Azarbaijan Shahid Madani University, Tabriz, Iran.
Abouzar NajafiDepartment of Animal Science and Poultry, Faculty of Agricultural Technology, University of Tehran, Tehran, Iran. abozar.najafi@ut.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study was to examine how gamma-oryzanol (GO) and gamma-oryzanol nanoparticles (GO-N) affected the quality of ram sperm after freeze-thaw treatment. Epididymal sperm from Shall rams collected from a slaughterhouse were diluted and divided into seven groups: a control group (0 µM), three concentrations of GO (50, 100, and 200 µM), and three concentrations of GO-N (50, 100, and 200 µM). The results demonstrated that treatment with 100 µM GO-N significantly improved the total motility (70.45%), progressive motility (60.21%), and velocity parameters (VCL, VSL, and VAP) compared to the other groups (p < 0.05). Plasma membrane and acrosomal integrity increased to 75.76% and 77.35%, respectively, while the percentage of morphological abnormalities decreased to 16.67% (p < 0.05). In the same group, flow cytometry revealed a reduction in DNA fragmentation to 17.22%, an increase in mitochondrial membrane potential to 66.11%, a decrease in H₂O₂ concentration to 13.29%, and the highest sperm viability (76.76%). MDA levels dropped to 3.42 nmol/mL, while SOD and GPx activities increased to 138.16 and 74.69 U/mg protein, respectively. Fertility assessments also indicated that the use of 100 µM GO-N in the extender significantly improved the pregnancy rate, lambing rate, and prolificacy compared with the other treatments (p < 0.05). In conclusion, the addition of 100 µM GO-N to the cryopreservation extender appears to be an effective strategy for enhancing the quality and functionality of thawed ram sperm, and may be valuable in breeding programs, reproductive biotechnology, and assisted reproductive technologies.

Indexed as

CryopreservationFertilityNanoparticlesPhenylpropionatesSemen PreservationSpermatozoaAnimalsCell SurvivalDNA FragmentationLiposomesMaleMembrane Potential, MitochondrialOxidative StressSheepSperm Motilitygamma-oryzanolLiposomesPhenylpropionatesAntioxidantsGamma oryzanolNanoliposomeOxidative stressSperm

Identifiers

PMID41942538
PMCPMC13212974

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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.