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呋喃妥因对哺乳动物细胞的细胞毒性和DNA损伤。

Cytotoxicity and DNA damage to mammalian cells by nitrofurans.

作者信息

Olive P L, McCalla D R

出版信息

Chem Biol Interact. 1977 Feb;16(2):223-33. doi: 10.1016/0009-2797(77)90131-4.

Abstract

Nitrofurazone, nitrofurantoin, furazolidone, furaltadone and N-[4-(5-nitro-2-furyl)-2-thiazolyl] formamide (FANFT) were toxic to cultured mouse L cells. The extent of toxocity and the rate of reduction of nitrofurazone increased markedly as the oxygen content of the incubation medium was lowered. The toxic effect of nitrofurans was decreased by addition of serum and was much greater in phosphate-buffered saline containing glucose (PSG) than in medium. Damage to L cell DNA by nitrofurans increased as the oxygen concentration decreased from 21% to 0%. The concentration of nitrofurazone and duration of exposure also determined the number of DNA single-strand breaks. It is suggested that toxicity and DNA damage may result from the actions of toxic intermediates in the metabolic reduction of nitrofurans.

摘要

呋喃西林、呋喃妥因、呋喃唑酮、呋咱甲氢龙和N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺(FANFT)对培养的小鼠L细胞有毒性。随着孵育培养基中氧含量的降低,呋喃西林的毒性程度和还原速率显著增加。添加血清可降低呋喃类药物的毒性作用,且在含葡萄糖的磷酸盐缓冲盐水(PSG)中比在培养基中的毒性作用大得多。随着氧浓度从21%降至0%,呋喃类药物对L细胞DNA的损伤增加。呋喃西林的浓度和暴露持续时间也决定了DNA单链断裂的数量。有人提出,毒性和DNA损伤可能是由于呋喃类药物代谢还原过程中有毒中间体的作用所致。

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