Evidence map›Paper›PMID 42270157›Full record

ArticleDevelopment, growth & differentiation

Computer-Aided Sperm Analysis Protocol for Evaluating Sperm Motility in Japanese Medaka.

Miwa Kuroyanagi, Satoshi Ansai, Keigo Okamoto, Ai Kato, Touko Yamazaki, Yasuhiro Kamei, Eiji Watanabe, Kiyoshi Naruse, Yukiko Ogino

Abstract read
In one paragraph

Article in Development, growth & differentiation. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Miwa KuroyanagiDepartment of Advanced Aquaculture Science, Faculty of Marine Bioscience and Technology, Fukui Prefectural University, Obama, Fukui, Japan.ORCID https://orcid.org/0000-0003-4362-8415
Satoshi AnsaiUshimado Marine Institute, Faculty of Science, Okayama University, Setouchi, Okayama, Japan.ORCID https://orcid.org/0000-0003-2683-0160
Keigo OkamotoLaboratory of Aquatic Molecular Developmental Biology, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Fukuoka, Japan.
Ai KatoInteruniversity Bio-Backup Project Center, National Institute for Basic Biology (NIBB), Okazaki, Aichi, Japan.
Touko YamazakiLaboratory of Bioresources, National Institutes of Natural Sciences, Okazaki, Aichi, Japan.
Yasuhiro KameiOptics and Bioimaging Facility, NIBB, Okazaki, Aichi, Japan.ORCID https://orcid.org/0000-0001-6382-1365
Eiji WatanabeBasic Biology Program, Graduate University for Advanced Studies (SOKENDAI), Okazaki, Aichi, Japan.
Kiyoshi NaruseLaboratory of Bioresources, National Institutes of Natural Sciences, Okazaki, Aichi, Japan.ORCID https://orcid.org/0000-0001-9185-3495
Yukiko OginoLaboratory of Aquatic Molecular Developmental Biology, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Fukuoka, Japan.ORCID https://orcid.org/0000-0003-3414-1648

Funding

Japan Society for the Promotion of Science JP19K06741Japan Society for the Promotion of Science JP20H04928Japan Society for the Promotion of Science JP24K01854Japan Society for the Promotion of Science JP24K02063Ministry of Education, Culture, Sports, Science and TechnologyNaito Foundation
6 · The paper itself

Abstract

Changes in sperm motility can serve as an early indicator of reproductive effects caused by environmental chemicals or genetic perturbations. However, sperm motility is highly sensitive to external factors such as osmolarity, ionic composition, and the timing of measurement after activation, making it challenging to obtain consistent and reproducible measurements. Here, we present a standardized protocol for assessing sperm motility in Japanese medaka (Oryzias latipes) using a sperm motility analysis system (SMAS), an application for computer-aided sperm motility analysis (CASA). This protocol details the procedures for sperm collection, activation, and quantitative motility assessment, with particular focus on changes in the percentage of motile sperm post activation and the effects of sperm cryopreservation. We demonstrate time-dependent declines in sperm motility and velocity, and highlight the importance of early post-activation measurements to accurately capture peak motility. Notably, cryopreservation significantly accelerated the decline in sperm motility rate without affecting the initial proportion of motile sperm. To enable reliable comparisons among experimental groups, we recommend standardizing the initiation time after sperm activation by using CASA, and show that measurements should be initiated within 1 min after activation to obtain consistent and reliable data. This standardized SMAS-based protocol provides a robust and reproducible framework for sperm motility analysis in medaka and will be valuable not only for studies in reproductive biology, toxicology, and environmental risk assessment but also for applied research, such as breeding of aquacultural fishes.

Indexed as

Image Processing, Computer-AssistedOryziasSemen AnalysisSpermatozoaSperm MotilityAnimalsCryopreservationMalecomputer‐aided sperm motility analysis (CASA)medakasperm motilitysperm motility analysis system (SMAS)

Identifiers

PMID42270157
PMCPMC13253179

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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.