Evidence map›Paper›PMID 35883101›Full record

ArticleStem cell research & therapy2022

Melatonin in cryopreservation media improves transplantation efficiency of frozen-thawed spermatogonial stem cells into testes of azoospermic mice.

Shokoofeh Kazemzadeh, Shahram Mohammadpour, Soheila Madadi, Azar Babakhani, Maryam Shabani, Maryam Khanehzad

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Melatonin: A Silver Bullet for Fertility and Reproductive Health.Reproductive sciences (Thousand Oaks, Calif.) · 2026
    Review
  3. Review
  4. Review
  5. New strategies for germ cell cryopreservation: Cryoinjury modulation.Clinical and experimental reproductive medicine · 2023
    Article
  6. Review
  7. Melatonin Supplementation duringAnimals : an open access journal from MDPI · 2023
    Article
  8. Review
  9. Article
4 · The record

Corrections and comments

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

6 authors at 4 institutions in 1 country.

Shokoofeh KazemzadehDepartment of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Shahram MohammadpourDepartment of Anatomy, School of Medicine, Ilam University of Medical Sciences, Ilam, Iran.
Soheila MadadiDepartment of Anatomy, School of Medicine, Arak University of Medical Sciences, Arak, Iran.
Azar BabakhaniDepartment of Anatomy, School of Medicine, Ilam University of Medical Sciences, Ilam, Iran.
Maryam ShabaniDepartment of Clinical Biochemistry, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Maryam KhanehzadDepartment of Anatomical Sciences and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran. m.khanehzad@med.mui.ac.ir.ORCID 0000-0001-7191-3745
Medical University of Ilam · IRTehran University of Medical Sciences · IRArak University of Medical Sciences · IRIsfahan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCryostorage of spermatogonial stem cells (SSCs) is an appropriate procedure for long-term storage of SSCs for fertility preservation. However, it causes damage to cellular structures through overproduction of ROS and oxidative stress. In this study, we examined the protective effect of melatonin as a potent antioxidant in the basic freezing medium to establish an optimal cryopreservation method for SSCs.

methodsSSCs were obtained from the testes of neonatal male mice aged 3-6 days. Then, 100 μM melatonin was added to the basic freezing medium containing DMSO for cryopreservation of SSCs. Viability, apoptosis-related markers (BAX and BCL2), and intracellular ROS generation level were measured in frozen-thawed SSCs before transplantation using the MTT assay, immunocytochemistry, and flow cytometry, respectively. In addition, Western blotting and immunofluorescence were used to evaluate the expression of proliferation (PLZF and GFRα1) and differentiation (Stra8 and SCP3) proteins in frozen-thawed SSCs after transplantation into recipient testes.

resultsThe data showed that adding melatonin to the cryopreservation medium markedly increased the viability and reduced intracellular ROS generation and apoptosis (by decreasing BAX and increasing BCL2) in the frozen-thawed SSCs (p < 0.05). The expression levels of proliferation (PLZF and GFRα1) and differentiation (Stra8 and SCP3) proteins and resumption of spermatogenesis from frozen-thawed SSCs followed the same pattern after transplantation.

conclusionsThe results of this study revealed that adding melatonin as an antioxidant to the cryopreservation medium containing DMSO could be a promising strategy for cryopreservation of SSCs to maintain fertility in prepubertal male children who suffer from cancer.

Indexed as

Adult Germline Stem CellsAzoospermiaMelatoninAnimalsAntioxidantsbcl-2-Associated X ProteinCryopreservationDimethyl SulfoxideFreezingHumansMaleMiceReactive Oxygen SpeciesSpermatogoniaTestisAntioxidantsbcl-2-Associated X ProteinDimethyl SulfoxideMelatoninReactive Oxygen SpeciesCryopreservationMelatoninSpermatogonial stem cellsTransplantation

Identifiers

PMID35883101
PMCPMC9327150
OpenAlexW4288053868

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.