Evidence map›Paper›PMID 34941713›Full record

ArticleToxins2021

Zearalenone Exposure Disrupts Blood-Testis Barrier Integrity through Excessive Ca

Jinjin She, Nannan Feng, Wanglong Zheng, Hao Zheng, Peirong Cai, Hui Zou, Yan Yuan, Jianhong Gu, Zongping Liu, Jianchun Bian

Open access · goldAbstract readComparative Study
In one paragraph

Article in Toxins, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Autophagy and the pancreas: Healthy and disease states.Frontiers in cell and developmental biology · 2024
    Review
  10. Article
  11. [Protective effects of total saponins fromNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Effect of Zearalenone-Induced Ferroptosis on Mice Spermatogenesis.Animals : an open access journal from MDPI · 2022
    Article
  17. Article
  18. 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

10 authors at 1 institution in 1 country.

Jinjin SheCollege of Veterinary Medicine, Yangzhou University, 12 Wenhui East Road, Yangzhou 225009, China.
Nannan FengCollege of Veterinary Medicine, Yangzhou University, 12 Wenhui East Road, Yangzhou 225009, China.
Wanglong ZhengCollege of Veterinary Medicine, Yangzhou University, 12 Wenhui East Road, Yangzhou 225009, China.ORCID 0000-0002-0939-331X
Hao ZhengCollege of Veterinary Medicine, Yangzhou University, 12 Wenhui East Road, Yangzhou 225009, China.
Peirong CaiCollege of Veterinary Medicine, Yangzhou University, 12 Wenhui East Road, Yangzhou 225009, China.
Hui ZouCollege of Veterinary Medicine, Yangzhou University, 12 Wenhui East Road, Yangzhou 225009, China.
Yan YuanCollege of Veterinary Medicine, Yangzhou University, 12 Wenhui East Road, Yangzhou 225009, China.
Jianhong GuCollege of Veterinary Medicine, Yangzhou University, 12 Wenhui East Road, Yangzhou 225009, China.
Zongping LiuCollege of Veterinary Medicine, Yangzhou University, 12 Wenhui East Road, Yangzhou 225009, China.ORCID 0000-0001-9071-8363
Jianchun BianCollege of Veterinary Medicine, Yangzhou University, 12 Wenhui East Road, Yangzhou 225009, China.ORCID 0000-0001-8023-0751
Yangzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zearalenone (ZEA), a common mycotoxin in grains and animal feeds, has been associated with male reproductive disorders. However, the potential toxicity mechanism of ZEA is not fully understood. In this study, in vivo and in vitro models were used to explore the effects of ZEA on the blood-testis barrier (BTB) and related molecular mechanisms. First, male BALB/C mice were administered ZEA orally (40 mg/kg·bw) for 5-7 d. Sperm motility, testicular morphology, and expressions of BTB junction proteins and autophagy-related proteins were evaluated. In addition, TM4 cells (mouse Sertoli cells line) were used to delineate the molecular mechanisms that mediate the effects of ZEA on BTB. Our results demonstrated that ZEA exposure induced severe testicular damage in histomorphology and an ultrastructural, time-dependent decrease in the expression of blood-testis barrier junction-related proteins, accompanied by an increase in the expression of autophagy-related proteins. Additionally, similar to the in vitro results, the dose-dependent treatment of ZEA increased the level of cytoplasmic Ca

Indexed as

AnimalsAutophagyBlood-Testis BarrierMaleMiceMice, Inbred BALB CMycotoxinsMyelin and Lymphocyte-Associated Proteolipid ProteinsSertoli CellsSperm MotilityTestisZearalenoneMycotoxinsMyelin and Lymphocyte-Associated Proteolipid ProteinsZearalenoneautophagyblood–testis barrierCa2+TM4 cellszearalenone

Identifiers

PMID34941713
PMCPMC8703826
OpenAlexW4200442816

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.