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Fluoride-induced unrestored arrest during haploid period of spermatogenesis via the regulation of DDX25 in rats

机译:氟化物诱导的单倍体生精的单倍体过程中DDX25的调节

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The effect of fluoride as an ongoing topic has attracted much attentions due to the decline in overall human fertility worldwide. However, whether fluorine causes a temporary stimulus or permanent damage to the male reproductive system, as well as the mechanism of fluoride influencing spermatogenesis remained unclear. 48 adult male rats were randomly divided into four groups (twelve each). Control group received the distilled water, while the other three groups were treated with 25, 50, 100 mg/L NaF via drinking water for 8 weeks. Six rats from each group were selected randomly to detect the levels of various indices related to spermatogenesis. The remaining rats were given only distilled water and left for recovery of a period of 2 weeks. Results showed that the levels of serum CK, ALP, CHE, BUN, UA, and Cr, testis morphology and the ultrastructure of sperm acrosome and chromatoid body (CB) were significantly changed by fluoride. Interestingly, the elongated spermatid counts, spermatids elongation ratio, and mRNA expressions of Prm1/2 and MIW1, TDRD1, TDRD 6, TDRD7, PABP, and Hsp72 related to CB decreased markedly in fluoride treatment groups compared to the control. Furthermore, the expression levels of DDX25 and associated regulatory proteins like CRM1, HMG2, H4, TP2, and PGK2 were down-regulated by fluoride. After 2-weeks withdrawal period, out of the 19 altered spermatogenesis indicators, 15 indicators in 100 mg/L group and 3 indicators in 50 mg/L group still exhibited a significant change, while none showed change in 25 mg/L group. These results proved that the reversibility of fluoride toxicity is dose-dependent on the male reproductive system. Meanwhile, fluoride caused unrestored arrest during the haploid period of spermatogenesis, where reduced DDX25 and associated regulatory proteins play a crucial role in this process, which could provide the underlying insights to the toxic mechanism of fluoride induced male reproductive toxicity. (C) 2019 Elsevier Ltd. All rights reserved.
机译:由于全球人类总生育力下降,氟化物作为一个持续的话题的影响已引起人们的广泛关注。但是,氟是否对男性生殖系统造成暂时性刺激或永久性损害,以及氟影响精子发生的机制尚不清楚。将48只成年雄性大鼠随机分为四组(每组十二只)。对照组接受蒸馏水,而其他三组分别通过饮用水分别以25、50、100 mg / L NaF处理8周。每组随机选择六只大鼠以检测与精子发生有关的各种指标的水平。剩余的大鼠仅被给予蒸馏水,并保留2周的时间。结果表明,氟化物显着改变了血清CK,ALP,CHE,BUN,UA和Cr的水平,睾丸的形态以及精子顶体和类染色体体的超微结构。有趣的是,与对照组相比,与CB相关的Prm1 / 2和MIW1,TDRD1,TDRD 6,TDRD7,PABP和Hsp72的延长精子数量,精子伸长率和mRNA表达与对照组相比明显降低。此外,DDX25和相关调节蛋白(如CRM1,HMG2,H4,TP2和PGK2)的表达水平被氟化物下调。停药2周后,在改变的19个精子发生指标中,100 mg / L组的15个指标和50 mg / L组的3个指标仍表现出显着变化,而25 mg / L组没有变化。这些结果证明,氟化物毒性的可逆性取决于男性生殖系统的剂量。同时,氟化物在精子发生的单倍体时期引起了未恢复的停滞,其中还原的DDX25和相关的调节蛋白在该过程中起着至关重要的作用,这可能为氟化物诱导的男性生殖毒性的毒性机制提供潜在的见解。 (C)2019 Elsevier Ltd.保留所有权利。

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