Evidence map›Paper›PMID 31430870›Full record

ArticleInternational journal of molecular sciences2019

Role of Autophagy in Zinc Oxide Nanoparticles-Induced Apoptosis of Mouse LEYDIG Cells.

Jingcao Shen, Dan Yang, Xingfan Zhou, Yuqian Wang, Shichuan Tang, Hong Yin, Jinglei Wang, Rui Chen, Jiaxiang Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
8.0field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Article
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  20. Biomimetic Construction of Artificial Selenoenzymes.Biomimetics (Basel, Switzerland) · 2023
    Review
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 at 3 institutions in 2 countries.

Jingcao ShenDepartment of Physiology, Medical College of Nanchang University, Nanchang 330006, China.
Dan YangDepartment of Physiology, Medical College of Nanchang University, Nanchang 330006, China.
Xingfan ZhouKey Laboratory of Occupational Health and Safety, Beijing Municipal Institute of Labor Protection, Beijing 100054, China.
Yuqian WangKey Laboratory of Occupational Health and Safety, Beijing Municipal Institute of Labor Protection, Beijing 100054, China.
Shichuan TangKey Laboratory of Occupational Health and Safety, Beijing Municipal Institute of Labor Protection, Beijing 100054, China.
Hong YinSchool of Aerospace, Mechanical and Manufacturing Engineering, RMIT University, Bundoora, VIC 3083, Australia.
Jinglei WangDepartment of Physiology, Medical College of Nanchang University, Nanchang 330006, China.
Rui ChenKey Laboratory of Occupational Health and Safety, Beijing Municipal Institute of Labor Protection, Beijing 100054, China. chenxiaorui@hotmail.com.ORCID 0000-0002-6488-6133
Jiaxiang ChenDepartment of Physiology, Medical College of Nanchang University, Nanchang 330006, China. chenjiaxiang@ncu.edu.cn.ORCID 0000-0003-0756-1647
Beijing Institute of Labor Protection Science · CNNanchang University · CNRMIT University · AU

Funding

National Natural Science Foundation of China No. 81660255, No. 81360098 and No. 21777036the Research fund for postgraduate program of Nanchang University No. cx2015179the Young Scientist Training Project of Jiangxi Province, China No. 20153BCB23032the Youth Plan of Beijing Academy of Science and Technology YC201809
6 · The paper itself

Abstract

Zinc oxide nanoparticles (ZnO NPs) have shown adverse health impact on the human male reproductive system, with evidence of inducing apoptosis. However, whether or not ZnO NPs could promote autophagy, and the possible role of autophagy in the progress of apoptosis, remain unclear. In the current study, in vitro and in vivo toxicological responses of ZnO NPs were explored by using a mouse model and mouse Leydig cell line. It was found that intragastrical exposure of ZnO NPs to mice for 28 days at the concentrations of 100, 200, and 400 mg/kg/day disrupted the seminiferous epithelium of the testis and decreased the sperm density in the epididymis. Furthermore, serum testosterone levels were markedly reduced. The induction of apoptosis and autophagy in the testis tissues was disclosed by up-regulating the protein levels of cleaved Caspase-8, cleaved Caspase-3, Bax, LC3-II, Atg 5, and Beclin 1, accompanied by down-regulation of Bcl 2. In vitro tests showed that ZnO NPs could induce apoptosis and autophagy with the generation of oxidative stress. Specific inhibition of autophagy pathway significantly decreased the cell viability and up-regulated the apoptosis level in mouse Leydig TM3 cells. In summary, ZnO NPs can induce apoptosis and autophagy via oxidative stress, and autophagy might play a protective role in ZnO NPs-induced apoptosis of mouse Leydig cells.

Indexed as

AnimalsApoptosisAutophagyCells, CulturedLeydig CellsMaleMiceNanoparticlesOxidative StressZinc OxideZinc OxideapoptosisautophagyLeydig cellsoxidative stressZnO NPs

Identifiers

PMID31430870
PMCPMC6720004
OpenAlexW2968531464

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.