| Literature DB >> 31125880 |
Xiuxiu Chen1, Qiqi Zhu1, Xiaoheng Li1, Tongliang Huang1, Songxue Wang1, Yiyan Wang1, Xianwu Chen1, Zhenkun Lin1, Ren-Shan Ge2.
Abstract
Tebuconazole is a triazole compound used agriculturally to treat plant pathogenic fungi. However, whether pubertal exposure to tebuconazole affects Leydig cell development remains unknown. Here, we exposed male Sprague-Dawley rats at 35 days of age to 0, 25, 50, or 100 mg kg-1 day-1 tebuconazole for 21 days. Tebuconazole exposure increased serum testosterone level but lowered estradiol level at a dose of 100 mg kg-1, without affecting serum luteinizing hormone and follicle-stimulating hormone concentrations. Tebuconazole up-regulated the expression of testicular Cyp11a1, Hsd11b1, and Fshr genes as well as their proteins at a dose of 100 mg kg-1. However, tebuconazole did not stimulate the proliferation of Leydig cells. Tebuconazole in vitro inhibits aromatase activity in primary rat Leydig cells with IC50 value of 40 μmol/L. In conclusion, tebuconazole exposure stimulates pubertal Leydig cell differentiation via inhibiting aromatase activity.Entities:
Keywords: Aromatase; Fungicide; Leydig cell; Rat; Tebuconazole; Testosterone
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Year: 2019 PMID: 31125880 DOI: 10.1016/j.chemosphere.2019.05.122
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086