Abstract

In a previous study oral administration of a commercial PCB mixture (Aroclor 1260) to female rabbits (4 mg/kg b.wt. for 14 weeks) resulted in a significant accumulation of PCBs in 6-d-old blastocysts and increased preimplantation embryo mortality (1). In the present study, the direct toxicity of PCBs on preimplantation rabbit embryos was investigated during in vitro culture. One-day-old cleavage stages and 3-d-old rabbit morulae were cultured in BSM II medium supplemented with 1.5% BSA in a reduced oxygen concentration of 5% O 2. They were exposed to 50, 5, or 0.5 μg Aroclor 1260/mL culture medium for 24 h. PCB (50 μg) led to a complete degeneration of the exposed embryos. Following exposure to 5 μg only 16% of the morulae developed into blastocysts. The others were either arrested in the morulae stage or were degenerated. Cell proliferation of the nondegenerated embryos was approximately 20% of that of corresponding control embryos. Compared with nonexposed controls, addition of 0.5 μg PCB/mL showed either no or only a slight impairment of development. Preliminary embryo transfer experiments showed that morulae exposed to 5 μg PCB with clear signs of degeneration after 24 h in vitro culture were able to implant. Aroclor 1260 is embryotoxic in a dose-dependent manner in cultured rabbit preimplantation embryos.

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