Kim Yong-Bin, Cheon Yong-Pil, Choi Donchan, Lee Sung-Ho
Dept. of Biotechnology, Sangmyung University, Seoul 03016, Korea.
Division of Developmental Biology and Physiology, School of Biological Sciences and Chemistry, Sungshin University, Seoul 02844, Korea.
Dev Reprod. 2020 Sep;24(3):159-165. doi: 10.12717/DR.2020.24.3.159. Epub 2020 Sep 30.
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 (<0.05). Pathohistological studies revealed that NP-treated F1 animals showed prominent increase in the ovarian follicle numbers (<0.01), and decrease in the diameter of uterine myometrium (<0.01), and increase in the diameter of luminal epithelium (<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.
此前,我们报道了低剂量壬基酚(NP)暴露对F1代雌性小鼠生殖参数的不良影响。在本研究中,我们进一步研究了NP暴露对F1代雌性小鼠生殖器官的病理组织学影响。从亲代交配前期直至F1代子代出生后第33天(PND 33)持续进行NP暴露以进行阴道检查。在PND 30处死小鼠并测量生殖组织重量。NP-50组动物的初始(PND 21)体重显著低于对照组动物,而在测量终末(PND 33)体重时体重差异得到恢复。在NP组动物中发现有早期阴道开口(<0.05)。病理组织学研究显示,经NP处理的F1代动物卵巢卵泡数量显著增加(<0.01),子宫肌层直径减小(<0.01),管腔上皮直径增加(<0.05)。本研究表明,亚慢性低剂量NP暴露诱导F1代小鼠青春期提前开始,并导致卵巢和子宫出现病理组织学异常。需要进一步研究以更好地了解NP在青春期启动中的作用机制,并找到避免NP暴露引发危险情况的方法。