Benbrook D M, Miller R V
Antimicrob Agents Chemother. 1986 Jan;29(1):1-6. doi: 10.1128/AAC.29.1.1.
Norfloxacin is a quinolone (pyridonecarboxylic acid derivative) effective against Pseudomonas aeruginosa infections. We studied the effects of this drug on DNA metabolism in P. aeruginosa. Norfloxacin inhibits DNA replication immediately on its addition to a logarithmically growing culture of P. aeruginosa. It inhibits the ability of P. aeruginosa DNA gyrase to supercoil relaxed, closed circular DNA in vitro. At intermediate concentrations of the drug, inhibition of DNA replication in vivo is followed by secondary (recovery) synthesis. Both recovery synthesis and the bactericidal effects of norfloxacin are dependent on continued protein synthesis, suggesting that these are inducible functions. Neither norfloxacin nor nalidixic acid induces Weigle-reactivation (inducible DNA repair) or mutagenesis in P. aeruginosa.
诺氟沙星是一种喹诺酮类(吡啶酮羧酸衍生物),对铜绿假单胞菌感染有效。我们研究了这种药物对铜绿假单胞菌DNA代谢的影响。诺氟沙星在添加到对数生长期的铜绿假单胞菌培养物中后立即抑制DNA复制。它在体外抑制铜绿假单胞菌DNA回旋酶使松弛的闭环DNA超螺旋化的能力。在药物的中间浓度下,体内DNA复制的抑制之后是二次(恢复)合成。诺氟沙星的恢复合成和杀菌作用均依赖于持续的蛋白质合成,这表明这些是可诱导的功能。诺氟沙星和萘啶酸均不会在铜绿假单胞菌中诱导韦格勒再活化(可诱导的DNA修复)或诱变。