Evidence mapPaperPMID 39948414Full record

ArticleScientific reports2025

Embryo vitrification impacts learning and spatial memory by altering the imprinting genes expression level in the mouse offspring' hippocampus.

Samira Hosseini, Sara Hosseini, Hadi Aligholi, Mohammad Salehi

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Samira HosseiniDepartment of Neuroscience, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran.
Sara HosseiniCellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Hadi AligholiDepartment of Neuroscience, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran. hadialigholi@yahoo.com.
Mohammad SalehiCellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran. msalehi78@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The safety and impact of embryo vitrification as a more reliable approach for cryopreservation in assisted reproductive techniques (ARTs) on the nervous system is uncertain. This study was aimed to investigate the expression level of imprinting genes in the hippocampus of offspring derived from vitrified embryo transfer. The hippocampus of the 2-day-old offspring from three experimental groups included vitrification (blastocysts derived from vitrified embryos), sham (the embryos at the blastocyst stage obtained through in vitro fertilization (IVF)) and control was removed for molecular, histological and behavioral analysis. There was no statistically noteworthy difference in survival, cleavage and blastocysts rate between vitrification and sham groups. Dnmt1, Dnmt3a, 3b and Igf2 upregulated in the vitrified group compared to the sham and control groups. The gene expression level of Meg3 declined dramatically and the intensity of DNA methylation in CpG island of Meg3 significantly elevated in the vitrification group. A notable disparity was observed in the quantity of dark neurons in the hippocampus of the offspring, spatial learning and memory abilities between the control and vitrification groups. According to these results, embryo vitrification may alters gene expression in brain hippocampus tissue and disturbs genomic imprinting, dark neuron formation and spatial memory.

Indexed as

Embryo, MammalianGenomic ImprintingHippocampusLearningSpatial MemoryVitrificationAnimalsBlastocystCpG IslandsCryopreservationDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesDNA MethylationDNA Methyltransferase 3ADNA Methyltransferase 3BEmbryo TransferDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNA Methyltransferase 3BIGF2 protein, mouseInsulin-Like Growth Factor IIMEG3 non-coding RNA, mouseRNA, Long NoncodingEmbryo vitrificationHippocampusImprinting genesMethylation

Identifiers

PMID39948414
PMCPMC11825692

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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.