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Gestational exposure to tebuconazole affects the development of rat fetal Leydig cells.

Abstract
Tebuconazole is a triazole fungicide, used in agriculture to treat phytopathogenic fungi, and as a biocide, has been reported to be related to reproductive and developmental toxicity. The purpose of this study was to investigate the effect of tebuconazole exposure on rat fetal Leydig cells and fetal testis during pregnancy. Pregnant Sprague-Dawley rats were randomly divided into 4 groups, daily gavaged with corn oil (as a control), 25, 50, and 100 mg/kg body weight tebuconazole for 10 days (from the 12th day of pregnancy). Tebuconazole increased fetal serum testosterone and progesterone levels at a dose of 100 mg/kg. Exposure to 100 mg/kg tebuconazole significantly caused an increase in the number of fetal Leydig cells per testis without inducing cell aggregation. Tebuconazole up-regulated the expression of Star, Cyp11a1, Hsd17b3, and Fshr and their proteins. Further investigation found that tebuconazole caused increased phosphorylation of AKT1, ERK1/2, and mTOR, the level of BCL2, as well as the decrease of Beclin1, LC3B, and BAX, which may contribute to the fetal Leydig cell autophagy and proliferation. In conclusion, in utero exposure of tebuconazole causes the proliferation of fetal Leydig cells.
AuthorsFeifei Ma, Yang Li, Yige Yu, Zengqiang Li, Liben Lin, Quanxu Chen, Qiang Xu, Peipei Pan, Yiyan Wang, Ren-Shan Ge
JournalChemosphere (Chemosphere) Vol. 262 Pg. 127792 (Jan 2021) ISSN: 1879-1298 [Electronic] England
PMID32805656 (Publication Type: Journal Article)
CopyrightCopyright © 2020 Elsevier Ltd. All rights reserved.
Chemical References
  • Fungicides, Industrial
  • Phosphoproteins
  • Triazoles
  • steroidogenic acute regulatory protein
  • Testosterone
  • tebuconazole
Topics
  • Animals
  • Female
  • Fungicides, Industrial (toxicity)
  • Leydig Cells (drug effects, metabolism)
  • Male
  • Phosphoproteins (genetics)
  • Phosphorylation
  • Pregnancy
  • Prenatal Exposure Delayed Effects (chemically induced, pathology)
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Reproduction (drug effects)
  • Testis (drug effects, embryology, pathology)
  • Testosterone (blood)
  • Triazoles (toxicity)
  • Up-Regulation

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