低剂量壬基酚处理F1雌性小鼠生殖系统组织学分析。

Development & reproduction Pub Date : 2020-09-01 Epub Date: 2020-09-30 DOI:10.12717/DR.2020.24.3.159
Yong-Bin Kim, Yong-Pil Cheon, Donchan Choi, Sung-Ho Lee
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引用次数: 8

摘要

此前,我们报道了低剂量壬基酚(NP)暴露对F1雌性小鼠生殖参数的不良影响。本研究进一步探讨NP暴露对F1雌性小鼠生殖器官的病理组织学影响。从亲代前交配期到F1子代出生后(PND) 33日,连续进行NP暴露以进行阴道检查。用PND 30处死小鼠,测定生殖组织重量。NP-50组动物的初始(PND 21)体重显著低于对照组动物,并在测量PND 33时恢复体重不足。NP组动物阴道早期开口(pppp)
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Histological Analysis of Reproductive System in Low-Dose Nonylphenol-treated F1 Female Mice.

Histological Analysis of Reproductive System in Low-Dose Nonylphenol-treated F1 Female Mice.

Histological Analysis of Reproductive System in Low-Dose Nonylphenol-treated F1 Female Mice.

Histological Analysis of Reproductive System in Low-Dose Nonylphenol-treated F1 Female Mice.

Previously, we reported adverse effects of low-dose nonylphenol (NP) exposure on the reproductive parameters of F1 female mice. In the present study we further investigated the pathohistological effect of NP exposure on the reproductive organs in F1 female mice. NP exposures were continuously conducted from parental pre-mating period until the postnatal day (PND) 33 of F1 offspring for vaginal examination. Mice were sacrificed on PND 30 and the reproductive tissue weights were measured. The initial (at PND 21) body weights of the NP-50 group animals were significantly lower than those of control group animals, and the weight deficit were recovered when the terminal (PND 33) body weights were measured. Early vaginal opening was found in NP group animals (p<0.05). Pathohistological studies revealed that NP-treated F1 animals showed prominent increase in the ovarian follicle numbers (p<0.01), and decrease in the diameter of uterine myometrium (p<0.01), and increase in the diameter of luminal epithelium (p<0.05). The present study demonstrated that the subchronic low-dose NP exposure induced early beginning of puberty and pathohistological abnormalities in ovary and uterus of F1 mice. Further studies are needed to achieve a better understanding on the action mechanism of NP in pubertal onset and to find a way to avoid a hazardous situation provoked by NP exposure.

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