Department of Zoology, Institute of Science, Banaras Hindu University, Varanasi, 221005, India.
Department of Zoology, Institute of Science, Banaras Hindu University, Varanasi, 221005, India.
Ecotoxicol Environ Saf. 2019 Nov 15;183:109499. doi: 10.1016/j.ecoenv.2019.109499. Epub 2019 Aug 6.
Perfluoroalkyl acids (PFAAs) are anthropogenic compounds used globally in a variety of commercial products. Perfluorononanoic acid (PFNA), a member of PFAAs, is detected in human blood and this has been reported to cause hepatotoxic, immunotoxic, and developmental and testicular toxic effects in laboratory animals. We have recently shown that the acute exposure to PFNA in prepubertal Parkes (P) mice impairs spermatogenesis by inducing oxidative stress and inhibiting testosterone biosynthesis in the testis. The present study was aimed to examine the effect of acute exposure to PFNA in prepubertal P mice on germ cell dynamics and to understand the possible mechanisms of action of this compound on testicular functions. PFNA (2 and 5 mg/kg body weight) was orally administered to male mice for 14 days from postnatal day 25-38. The treatment caused a decrease in overall germ cell transformation. The results also reveal that impairment in testicular functions in treated mice is associated with alterations in cholesterol and glucose homeostasis; further, an inhibition in expressions of growth hormone receptor (GHR), insulin-like growth factor-1 (IGF-1), insulin-like growth factor-1 receptor (IGF-1R), androgen receptor (AR), phosphorylated mammalian target of rapamycin (p-mTOR) and peroxisome proliferator activated receptor α (PPAR α) in the testis is also implicated in this action. The findings thus suggest involvement of multiple factors which altogether contribute to the alterations in spermatogenic process and testosterone production following acute exposure to PFNA in prepubertal mice.
全氟烷基酸(PFAAs)是一种人为合成的化合物,广泛应用于各种商业产品中。全氟壬酸(PFNA)是 PFAAs 的一种成员,已在人类血液中被检测到,并且据报道,它会对实验动物的肝脏、免疫系统和生殖系统造成毒性作用。我们最近发现,青春期前 Parkes(P)小鼠急性暴露于全氟壬酸会通过诱导睾丸中的氧化应激和抑制睾酮生物合成来损害精子发生。本研究旨在研究青春期前 P 小鼠急性暴露于全氟壬酸对生殖细胞动力学的影响,并了解该化合物对睾丸功能的可能作用机制。从出生后第 25-38 天起,将 2 和 5mg/kg 体重的全氟壬酸经口给予雄性小鼠 14 天。该处理导致整体生殖细胞转化减少。结果还表明,处理小鼠的睾丸功能受损与胆固醇和葡萄糖稳态的改变有关;此外,睾丸中生长激素受体(GHR)、胰岛素样生长因子-1(IGF-1)、胰岛素样生长因子-1 受体(IGF-1R)、雄激素受体(AR)、磷酸化雷帕霉素靶蛋白(p-mTOR)和过氧化物酶体增殖物激活受体 α(PPAR α)的表达抑制也与此作用有关。这些发现表明,多种因素共同参与了青春期前小鼠急性暴露于全氟壬酸后精子发生过程和睾酮产生的改变。