Evidence map›Paper›PMID 39747170›Full record

ArticleScientific reports2025

Method for long-term room temperature storage of mouse freeze-dried sperm.

Yuko Kamada, Kango Yamaji, Natsuki Ushigome, Daiyu Ito, Sayaka Wakayama, Kenichiro Hiraoka, Masaru Hayashi, Kiyotaka Kawai, Teruhiko Wakayama

Abstract read
In one paragraph

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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Freeze-Drying and Room Temperature Preservation of Mammalian Sperm.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  5. Article
  6. Article
  7. Can Humanity Thrive Beyond the Galaxy?The Journal of reproduction and development · 2025
    Review
  8. 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

9 authors.

Yuko KamadaFaculty of Life and Environmental Science, University of Yamanashi, Yamanashi, Japan.
Kango YamajiFaculty of Life and Environmental Science, University of Yamanashi, Yamanashi, Japan.
Natsuki UshigomeFaculty of Life and Environmental Science, University of Yamanashi, Yamanashi, Japan.
Daiyu ItoFaculty of Life and Environmental Science, University of Yamanashi, Yamanashi, Japan.
Sayaka WakayamaAdvanced Biotechnology Center, University of Yamanashi, Yamanashi, Japan.
Kenichiro HiraokaDepartment of Reproductive Medicine, Kameda Medical Center (Kameda General Hospital), Chiba, Japan.
Masaru HayashiDepartment of Reproductive Medicine, Kameda Medical Center (Kameda General Hospital), Chiba, Japan.
Kiyotaka KawaiDepartment of Reproductive Medicine, Kameda Medical Center (Kameda General Hospital), Chiba, Japan.
Teruhiko WakayamaFaculty of Life and Environmental Science, University of Yamanashi, Yamanashi, Japan. twakayama@yamanashi.ac.jp.

Funding

Asada Science Fundation Teruhiko Wakayamacanon foundation M20-0008Japan Science and Technology Agency JPMJSP2133Japan Society for the Promotion of Science 23K08843Japan Society for the Promotion of Science 23K18124Japan Society for the Promotion of Science JP20J23364Naito Foundation Sayaka WakayamaTakahashi Industrial and Economic Research Foundation 189
6 · The paper itself

Abstract

Permanent preservation of genetic resources may be indispensable for the future of humanity. This requires liquid nitrogen, as is the case for preserving animal sperm. However, this technique is expensive and poses a risk of irrecoverable sample loss on non-replenishment of liquid nitrogen in case of natural disasters. In this study, we demonstrate that lyophilization may be used as a reliable method for long-term preservation of mouse sperm at room temperature. Sperm from four mouse strains were freeze-dried and stored in a non-temperature controlled room for 5-6 years. Although the ability of the stored sperm to activate oocytes had diminished slightly, healthy offspring were obtained by artificially activating the oocytes after sperm injection. Moreover, the birth rate did not decrease even after ≤ 6 years of storage. Furthermore, owing to its low cost, safety, and ease of storage at any location, we believe that this method could be a major mode of preserving mammalian genetic resources in the future.

Indexed as

Freeze DryingSemen PreservationSpermatozoaTemperatureAnimalsCryopreservationFemaleMaleMiceOocytesSperm Injections, IntracytoplasmicFreeze-dryingGenetic resourcesOocyte activationRoom temperatureSperm preservation

Identifiers

PMID39747170
PMCPMC11695616

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.