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[3,6-二(二甲基氨基)二苯并碘鎓与柠檬酸镨复合物对小鼠白血病L 7712细胞DNA、RNA、蛋白质、核蛋白及ATP合成的影响]

[Effects of complex of 3,6-di-(dimethylamino)-dibenzopyriodonium with praseodymium dicitrate on the syntheses of DNA, RNA, protein, nucleoprotein and ATP of leukemia L 7712 cells in mice].

作者信息

Liu L S, Wang P, Wang S Z, Zheng R L, Zhang L D, Chen S Y, Wang C H, Hou Z J

出版信息

Zhongguo Yao Li Xue Bao. 1989 Mar;10(2):188-91.

PMID:2816422
Abstract

The incorporations of [3H] thymidine, [3H]uridine and [3H]leucine into DNA, RNA and protein synthesis in leukemia 7712 cells were inhibited by the complex of 3,6-di-(dimethylamino)-dibenzopyriodonium with praseodymium (Pr, rare earth element) dicitrite 34 micrograms/ml for 3-24 h. The degree of inhibition increased in proportion to the incubation time. After being treated with [C17H20N2I]3[Pr(C6H5O7)2] 34 micrograms/ml for 3, 6, 12 and 24 h, the incorporation of [32P]Na2HPO4 into the nucleoprotein of leukemia 7712 cells was inhibited by 49, 57, 65 and 85%, while those into ATP were inhibited by 43, 59, 65 and 83%, respectively. The ID50 of [C17H20N2I]3[Pr(C6H5O7)2] on DNA synthesis in leukemia 7712 cells at 24 h was 22 micrograms/ml. After the complex was removed from the medium entirely, the rate of DNA synthesis decreased with time over 3-12 h. This result indicated that the inhibition mechanism was likely due to damage to the DNA template.

摘要

3,6-二(二甲基氨基)二苯并碘鎓与柠檬酸镨(Pr,稀土元素)形成的配合物,浓度为34微克/毫升,作用3至24小时,可抑制白血病7712细胞中[3H]胸苷、[3H]尿苷和[3H]亮氨酸掺入DNA、RNA和蛋白质合成。抑制程度随孵育时间成比例增加。用34微克/毫升的[C17H20N2I]3[Pr(C6H5O7)2]处理3、6、12和24小时后,白血病7712细胞核蛋白中[32P]Na2HPO4的掺入分别被抑制49%、57%、65%和85%,而掺入ATP的分别被抑制43%、59%、65%和83%。[C17H20N2I]3[Pr(C6H5O7)2]在24小时对白血病7712细胞DNA合成的半数抑制浓度(ID50)为22微克/毫升。将该配合物从培养基中完全去除后,在3至12小时内DNA合成速率随时间下降。该结果表明抑制机制可能是由于对DNA模板的损伤。

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