Abstract

Biochemical studies on effects of methylmercury and inorganic mercury on mouse glioma and neuroblastoma cells were carried out. Inorganic mercury accelerated DNA synthesis of mouse glioma cells at 10 −6 to 10 −5 m specifically in the middle log phase of the growth. Inorganic mercury facilitated the thymidine and deoxycytidine transports within a narrow range of concentration (1 to 2 × 10 −5 m), but no stimulation of transport was observed in the cases of purine deoxyribonucleosides. Inorganic mercury markedly inhibited both DNA synthesis and the transport systems of the precursors above 5 × 10 −5 m. On the other hand, methylmercury showed hardly any accelerating effects and markedly inhibited both the synthesis of DNA and the precursors' transport above 5 × 10 −5 m. In the case of mouse neuroblastoma cells, inorganic mercury stimulated DNA synthesis at 1 to 5 × 10 −6 m and also thymidine transport system at 1 to 2 × 10 −5 m.

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