Chang C H, Yarbro J W, Mann D E, Gautieri R F
J Pharmacol Exp Ther. 1978 Apr;205(1):27-32.
The effects of 1,10-phenanthroline and a zinc complex of 1,10-phenanthroline on nucleic acid synthesis were examined by noting the capcity of these agents to incorporate [methyl-3H]thymidine, or [5-3H]uridine into hepatic and splenic DNA and RNA. Within 32 hours after the intraperitoneal injection of 1,10-phenanthroline in mice, a decrease of [methyl-3H]thymidine incorporation into hepatic DNA was observed. The administration of the zinc complex of 1,10-phenanthroline decreased the incorporation of [5-3H] uridine into hepatic RNA within 24 hours and decreased the formation of [3H]DNA from [methyl-3H]thymidine in the liver within 24 and 32 hours. An increase of the isotopic incorporation into hepatic RNA and of the pool size of ATP within 2 hours after the administration of the complex was also noted. In the splenic studies, the zinc complex significantly inhibited the formation of labeled DNA and RNA at 2, 8, 24, and 32 and 2, 8 and 24 hours postinjection, respectively. A relationship exists between the results obtained from sequential treatment (zinc chloride after 1,10-phenanthroline) and those derived from the zinc complex of 1,10-phenanthroline pertaining to an inhibition of isotopic incorporation into hepatic and splenic nucleic acid.
通过观察1,10 - 菲咯啉及其锌配合物将[甲基 - ³H]胸苷或[5 - ³H]尿苷掺入肝脏和脾脏DNA及RNA中的能力,研究了它们对核酸合成的影响。给小鼠腹腔注射1,10 - 菲咯啉后32小时内,观察到[甲基 - ³H]胸苷掺入肝脏DNA的量减少。1,10 - 菲咯啉锌配合物给药后24小时内,[5 - ³H]尿苷掺入肝脏RNA的量减少,给药后24小时和32小时,肝脏中[甲基 - ³H]胸苷形成[³H]DNA的量减少。给药后2小时内,还观察到该配合物使肝脏RNA的同位素掺入量增加以及ATP池大小增加。在脾脏研究中,锌配合物分别在注射后2、8、24和32小时以及2、8和24小时显著抑制标记DNA和RNA的形成。连续给药(1,10 - 菲咯啉后给予氯化锌)和给予1,10 - 菲咯啉锌配合物所获得的结果之间存在关联,二者均涉及抑制同位素掺入肝脏和脾脏核酸。