PMID- 28007637 OWN - NLM STAT- MEDLINE DCOM- 20170207 LR - 20240327 IS - 1879-3169 (Electronic) IS - 0378-4274 (Print) IS - 0378-4274 (Linking) VI - 266 DP - 2017 Jan 15 TI - Reproductive toxicity of linuron following gestational exposure in rats and underlying mechanisms. PG - 49-55 LID - S0378-4274(16)33356-2 [pii] LID - 10.1016/j.toxlet.2016.12.013 [doi] AB - Linuron is a widely used herbicide in agriculture; its endocrine disruptive toxicity has recently received public attention. This study was designed to examine the developmental toxicity of linuron on the reproductive system of male offspring following maternal exposure. Mother rats received oral gavages of linuron, once daily, at the dose of 0, 50, 100, 150 or 200mg/kg, from gestational day (GD)13 to GD18; gonadal organs from GD20 fetuses were examined. Data indicated that exposed male offspring had a significantly shortened anogenital distance. Pathological examination further revealed a lack of fusion in the urogenital fold in treated fetuses, the damaged seminiferous tubules, and the injured Leydig cell ultrastructure. Analysis of serum testosterone concentrations at postnatal day (PND)2 showed a significant dose-related reduction (about 33.7-58.75%, r=-0.838, p<0.05) as compared to controls. Immunohistochemical results demonstrated a significantly reduced expression of enzymes pertinent to the testosterone production including P450scc, 3beta-HSD, and PCNA in Leydig cells (p<0.05). qPCR studies confirmed decreased levels of mRNAs encoding P450scc, 3beta-HSD and PCNA (p<0.05). Taken together, these data suggest that maternal exposure to linuron hampers the male gonadal organ development; this appears to be due to linuron's direct action on the production of testosterone in fetal and postnatal offspring. CI - Copyright (c) 2016 Elsevier Ireland Ltd. All rights reserved. FAU - Ding, Hongwei AU - Ding H AD - Department of Hygiene Toxicology, School of Public Health, Zunyi Medical College, Zunyi, Guizhou, PR China. FAU - Zheng, Wei AU - Zheng W AD - School of Health Sciences, Purdue University, West Lafayette, IN, USA. FAU - Han, Hua AU - Han H AD - Department of Hygiene Toxicology, School of Public Health, Zunyi Medical College, Zunyi, Guizhou, PR China. FAU - Hu, Xiyin AU - Hu X AD - Department of Hygiene Toxicology, School of Public Health, Zunyi Medical College, Zunyi, Guizhou, PR China. FAU - Hu, Binli AU - Hu B AD - Department of Hygiene Toxicology, School of Public Health, Zunyi Medical College, Zunyi, Guizhou, PR China. FAU - Wang, Feng AU - Wang F AD - Department of Hygiene Toxicology, School of Public Health, Zunyi Medical College, Zunyi, Guizhou, PR China. FAU - Su, Liyu AU - Su L AD - Department of Hygiene Toxicology, School of Public Health, Zunyi Medical College, Zunyi, Guizhou, PR China. FAU - Li, Hong AU - Li H AD - Department of Hygiene Toxicology, School of Public Health, Zunyi Medical College, Zunyi, Guizhou, PR China. FAU - Li, Yan AU - Li Y AD - Department of Hygiene Toxicology, School of Public Health, Zunyi Medical College, Zunyi, Guizhou, PR China. Electronic address: liyan067321@sina.com. LA - eng GR - R01 ES008146/ES/NIEHS NIH HHS/United States PT - Journal Article DEP - 20161219 PL - Netherlands TA - Toxicol Lett JT - Toxicology letters JID - 7709027 RN - 0 (Herbicides) RN - 01XP1SU59O (Linuron) RN - 3XMK78S47O (Testosterone) SB - IM MH - Animals MH - Animals, Newborn MH - Dose-Response Relationship, Drug MH - Female MH - Genitalia, Male/drug effects MH - Herbicides/administration & dosage/*toxicity MH - Linuron/administration & dosage/*toxicity MH - Male MH - Pregnancy MH - Prenatal Exposure Delayed Effects MH - Rats MH - Rats, Sprague-Dawley MH - Testosterone/blood PMC - PMC5697898 MID - NIHMS917152 OTO - NOTNLM OT - Developmental toxicity OT - Fetus OT - Leydig cells OT - Linuron OT - Offspring OT - Reproductive toxicity OT - Testosterone COIS- Conflict of interest None. EDAT- 2016/12/23 06:00 MHDA- 2017/02/09 06:00 PMCR- 2017/11/21 CRDT- 2016/12/24 06:00 PHST- 2016/08/05 00:00 [received] PHST- 2016/12/10 00:00 [revised] PHST- 2016/12/18 00:00 [accepted] PHST- 2016/12/23 06:00 [pubmed] PHST- 2017/02/09 06:00 [medline] PHST- 2016/12/24 06:00 [entrez] PHST- 2017/11/21 00:00 [pmc-release] AID - S0378-4274(16)33356-2 [pii] AID - 10.1016/j.toxlet.2016.12.013 [doi] PST - ppublish SO - Toxicol Lett. 2017 Jan 15;266:49-55. doi: 10.1016/j.toxlet.2016.12.013. Epub 2016 Dec 19.