Effects of Tributyltin Chloride on Developing Mouse Oocytes and Preimplantation Embryos

Abstract

Tributyltin, an organotin, is ubiquitous in estuaries and freshwater systems. Previous reports suggest that tributyltin is an endocrine disruptor in many wildlife species and it inhibits aromatase in mammalian placental and granulosa-like tumor cell lines. However, no evidence showing the effects of tributyltin on oocytes or preimplantation embryonic developmental competence exists. Therefore, we investigated the role of tributyltin chloride (TBTCl) in the development of female oocytes and preimplantation embryos. Briefly, female ICR mice were gavaged with 0 (vehicle), 4, and 8 mg/kg of TBTCl each day for 18 days. The fluorescence intensity analysis showed that the 5-methylcytosine level decreased after TBTCl treatment, indicating that the general DNA methylation level decreased in the treated oocytes. Our results demonstrate that TBTCl treatment results in decreased mRNA levels of imprinted genes H19, Igf2r, and Peg3 during oocyte growth. The TBTCl-treated oocytes showed a significant increase in reactive oxygen species levels in germinal vesicle oocytes. In TBTCl-treated oocytes, there was no difference in GPx and Sod1 expression, but a decreased mRNA level of Cat occurred when compared with control. Moreover, the blastocysts with TBTCl exposure displayed higher apoptotic signals. These results suggest that TBTCl induces developmental defects in oocytes and preimplantation embryos.

Tributyltin oxide exposure impairs mouse oocyte maturation and its possible mechanisms

“…Studies also indicate that ROS plays a crucial role in inducing apoptosis. Additionally, studies indicate Tributyltin chloride can cause oxidative damage by increasing the gene expression level of Sod1 , Cat , and Gpx . As expected in our research, ROS generation was evaluated and the level was increased significantly after TBTO exposure.…”

“…Additionally, studies indicate Tributyltin chloride can cause oxidative damage by increasing the gene expression level of Sod1, Cat, and Gpx. 16,43 As expected in our research, ROS generation was evaluated and the level was increased significantly after TBTO exposure. Also, we found that TBTO could induce apoptosis.…”