Evidence map›Paper›PMID 37842186›Full record

ArticleAnimal cells and systems2023

Effects of prenatal bisphenol S and bisphenol F exposure on behavior of offspring mice.

Ha Jung Moon, Hyun Seung Shin, Seung Hyun Lee, Eui-Ju Hong, Changhwan Ahn, Yeong-Min Yoo, Eui-Bae Jeung, Geun-Shik Lee, Beum-Soo An, Eui-Man Jung

Open access · goldAbstract read
In one paragraph

Article in Animal cells and systems, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
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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

10 authors at 6 institutions in 1 country.

Ha Jung MoonDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Busan, Republic of Korea.
Hyun Seung ShinDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Busan, Republic of Korea.
Seung Hyun LeeDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Busan, Republic of Korea.
Eui-Ju HongDepartment of Veterinary Medicine, Chungnam National University, Daejeon, Republic of Korea.
Changhwan AhnDepartment of Veterinary Medicine, Jeju National University, Jeju, Republic of Korea.
Yeong-Min YooEast Coast Life Sciences Institute, College of Life Science, Gangneung-Wonju National University, Gangneung, Republic of Korea.
Eui-Bae JeungLaboratory of Veterinary Biochemistry and Molecular Biology, Veterinary Medical Center and College of Veterinary Medicine, Chungbuk National University, Cheongju, Republic of Korea.
Geun-Shik LeeDepartment of Veterinary Medicine, Kangwon National University, Chuncheon, Republic of Korea.
Beum-Soo AnDepartment of Biomaterials Science (BK21 Four Program), College of Natural Resources & Life Science, Pusan National University, Miryang, Republic of Korea.
Eui-Man JungDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Busan, Republic of Korea.
Pusan National University · KRChungbuk National University · KRChungnam National University · KRGangneung–Wonju National University · KRJeju National University · KRKangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bisphenol A (BPA) is a representative endocrine-disrupting chemical that exhibits hormonal disturbance reactions. Various alternatives, such as Bisphenol S (BPS) and Bisphenol F (BPF), are being developed. BPS and BPF (which are representative alternatives to BPA) are used in consumer products such as polycarbonate plastics and epoxy resins. They have structures similar to those of BPA and have also been proven to be exogenous endocrine disruptors. However, although there are many studies on BPA, there are few studies on the neurodevelopmental effects of BPS and BPF. Therefore, in this study, we analyzed neurobehavioral changes in offspring mice exposed to BPS and BPF during brain development by administering BPS and BPF to pregnant mice. We found that prenatal exposure to BPS and BPF did not affect anxiety-and depression-like behaviors, locomotion, sociability, memory, or cognition functions in offspring mice. However, exposure to BPS and BPF decreased the preference for social novelty in the offspring mice. Taken together, these findings suggest that perinatal exposure to BPS and BPF affects changes in social behaviors, but not other behavioral changes such as emotion, memory, or cognition in the offspring mice.

Indexed as

BPFBPSbrain developmentEndocrine disrupting chemicals

Identifiers

PMID37842186
PMCPMC10572065
OpenAlexW4387575603

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.