Evidence map›Paper›PMID 42015274›Full record

ArticleBiology direct2026

Toxicological effects of acrylamide on oocyte maturation and subsequent embryonic development in a porcine model.

Na-Gyeom Oh, Pil-Soo Jeong, Hyo-Gu Kang, Se-Been Jeon, Ji Hyeon Yun, Se-Yeon Eom, Sun-Uk Kim, Seong-Keun Cho, Bo-Woong Sim

Abstract read
In one paragraph

Article in Biology direct, 2026. 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
0cells of the map it votes in
0citing 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

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.

Na-Gyeom Oh *Futuristic Animal Resource & Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Republic of Korea.
Pil-Soo Jeong *Futuristic Animal Resource & Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Republic of Korea.
Hyo-Gu KangFuturistic Animal Resource & Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Republic of Korea.
Se-Been JeonFuturistic Animal Resource & Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Republic of Korea.
Ji Hyeon YunFuturistic Animal Resource & Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Republic of Korea.
Se-Yeon EomFuturistic Animal Resource & Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Republic of Korea.
Sun-Uk KimFuturistic Animal Resource & Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Republic of Korea.
Seong-Keun ChoDepartment of Animal Science, College of Natural Resources & Life Science, Pusan National University, Miryang, 50463, Republic of Korea. skcho@pusan.ac.kr.
Bo-Woong SimFuturistic Animal Resource & Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, 28116, Republic of Korea. embryont@kribb.re.kr.

Funding

Korea Research Institute of Bioscience and Biotechnology KGM1012622Korea Research Institute of Bioscience and Biotechnology KQM0042611National Research Foundation of Korea RS-2021-NR057659
6 · The paper itself

Abstract

backgroundAcrylamide (ACR) is a highly water-soluble vinyl monomer that is widely used in industrial applications. It can be released into aquatic environments through industrial effluents and subsequently transported into soil and groundwater. In addition to environmental exposure, ACR is formed during high-temperature cooking processes. Although ACR is well documented to exert neurotoxic, genotoxic, and carcinogenic effects, its impact on the female reproductive system remains insufficiently characterized.

resultsThis study investigated the effects of ACR exposure during in vitro maturation (IVM) on porcine oocyte meiotic maturation and subsequent embryonic development following parthenogenetic activation. ACR exposure significantly reduced the proportion of matured oocytes and downregulated the transcriptional levels of genes associated with oocyte maturation compared with controls. Furthermore, ACR treatment during IVM markedly compromised embryonic developmental parameters, as evidenced by decreased cleavage rates; reduced proportions of two-cell, four-cell, and morula-stage embryos; a lower blastocyst formation rate; and an increased fragmentation rate relative to controls. ACR exposure during IVM also impaired blastocyst quality, as indicated by reduced total cell numbers and an elevated apoptosis rate compared with controls. In addition, ACR exposure disrupted cell cycle progression and cytoskeletal integrity. Moreover, ACR treatment increased levels of reactive oxygen species while decreasing glutathione content and mitochondrial abundance compared with controls. ACR exposure also elevated DNA damage, autophagy, and early apoptosis in oocytes.

conclusionsACR exposure during IVM exerts detrimental effects on porcine oocyte meiotic maturation and subsequent embryonic development by inducing cell cycle arrest, oxidative stress, DNA damage, excessive autophagy, and early apoptosis.

Indexed as

AcrylamideEmbryonic DevelopmentOocytesAnimalsApoptosisFemaleIn Vitro Oocyte Maturation TechniquesOxidative StressParthenogenesisSwineAcrylamideAcrylamideApoptosisCytoskeletal integrityDNA damageOxidative stressPorcine oocyte maturation

Identifiers

PMID42015274
PMCPMC13235154

What OpenQuestion holds

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Registered trials

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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.