Evidence map›Paper›PMID 27267904›Full record

ArticleReproductive biology and endocrinology : RB&E2016

Involvement of oxidative stress in tri-ortho-cresyl phosphate-induced autophagy of mouse Leydig TM3 cells in vitro.

Xiaomei Liu, Linlin Xu, Jingcao Shen, Jinglei Wang, Wenli Ruan, Mei Yu, Jiaxiang Chen

Open access · goldAbstract read
In one paragraph

Article in Reproductive biology and endocrinology : RB&E, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Review
  3. DAPK3 is Essential for DBP-Induced Autophagy of Mouse Leydig Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

7 authors at 1 institution in 1 country.

Xiaomei LiuDepartment of Physiology, Medical College of Nanchang University, 461 Bayi Road, Donghu District, Nanchang, 330006, People's Republic of China.
Linlin XuMedical Research Center, The First Affiliated Hospital of Nanchang University, Nanchang, 330006, People's Republic of China.
Jingcao ShenDepartment of Physiology, Medical College of Nanchang University, 461 Bayi Road, Donghu District, Nanchang, 330006, People's Republic of China.
Jinglei WangDepartment of Physiology, Medical College of Nanchang University, 461 Bayi Road, Donghu District, Nanchang, 330006, People's Republic of China.
Wenli RuanDepartment of Physiology, Medical College of Nanchang University, 461 Bayi Road, Donghu District, Nanchang, 330006, People's Republic of China.
Mei YuLibrary, Medical College of Nanchang University, Nanchang, 330006, People's Republic of China.
Jiaxiang ChenDepartment of Physiology, Medical College of Nanchang University, 461 Bayi Road, Donghu District, Nanchang, 330006, People's Republic of China. chenjiaxiang@ncu.edu.cn.
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs a plasticizer, plastic softener, and flame-retardant, tri-ortho-cresyl phosphate (TOCP) is and has been widely used in industry and reported to have a toxic effect on the male reproductive system in animals besides neurotoxicity and immunotoxicity. We have reported that TOCP inhibits spermatogenesis and induces autophagy of rat spermatogonial stem cells, but it is still unknown whether TOCP induces autophagy of mouse Leydig cells and its potential mechanism.

methodsCell viability was observed by MTT assay. Level of testosterone was measured by radioimmunoassay. Apoptosis was observed by AnnexinV-FITC/PI assay. The contents of LC3, Atg5-Atg12, and Beclin 1 were detected by Western blotting analysis. Autophagosomes were investigated by transmission electron microscopy. The contents of MDA and GSH and the activities of SOD, GSH-PX, total antioxidant status (TAS) and total oxidant status (TOS) were measured by oxidative stress kits.

resultsThe present study shows that TOCP markedly inhibited viability and testosterone output of mouse Leydig TM3 cells but had no effect on apoptosis. However, TOCP significantly increased both LC3-II and the ratio of LC3-II to LC3-I and the contents of autophagy proteins Atg5 and Beclin 1. Transmission electron microscopy (TEM) showed that TOCP increased autophagic vacuoles of the cytoplasm, indicating that TOCP could induce autophagy of the cells. TOCP significantly induced oxidative stress of mouse Leydig TM3 cells. H2O2 also inhibited viability and induced autophagy of the cells; however, inhibition of oxidative stress by N-acetyl-L-cysteine (NAC) could rescue the inhibition of cell viability and induction of autophagy by TOCP.

conclusionsThe results show oxidative stress might be involved in TOCP-induced autophagy of mouse Leydig TM3 cells.

Indexed as

Oxidative StressAnimalsApoptosisAutophagyCells, CulturedHydrogen PeroxideLeydig CellsMaleMicePlasticizersSpermatogenesisTestosteroneToxicity TestsTritolyl PhosphatesVacuolesHydrogen PeroxidePlasticizersTestosteronetri-o-cresyl phosphateTritolyl PhosphatesAutophagyLeydig cellsOxidative stressTri-ortho–cresyl phosphate

Identifiers

PMID27267904
PMCPMC4897823
OpenAlexW2411063739

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.