精神药物治疗质粒的新机制。

J Molnár, B Schneider, Y Mándi, S Farkas, I B Holland
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引用次数: 0

摘要

亚甲基蓝对携带F-prime lac或耐药因子R-144的大肠杆菌K12菌株增强了氯丙嗪、丙咪嗪和阿米替林的质粒固化效率。相比之下,亚甲基蓝在所有浓度下都能抑制吖啶橙和溴化乙酯对质粒的清除。氯丙嗪的两种代谢衍生物——亚砜氯丙嗪和7.8-二氧氯丙嗪在亚甲基蓝存在下也没有质粒固化作用。阿米替林、7,8-二氧氯丙嗪和吖啶橙是抗性质粒R-144共轭转移的有效抑制剂,而亚甲基蓝、亚砜氯丙嗪和丙咪嗪只有轻微的作用。因此,我们无法证明治疗能力和抑制质粒转移之间的简单相关性在精神活性药物测试。提出了一种通过药物表面作用固化质粒的机制,作为直接嵌入质粒DNA的替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New mechanism of plasmid curing by psychotropic drugs.

Methylene blue enhanced the plasmid curing efficiency of chlorpromazine, imipramine and amitriptyline with strains of Escherichia coli K12 carrying F-prime lac or the resistance factor R-144. In contrast, methylene blue inhibited the elimination of plasmids by acridine orange and ethydium bromide at all concentrations tested. Two metabolic derivatives of chlorpromazine, chlorpromazine sulphoxide and 7.8-dioxochlorpromazine had no plasmid curing effect even in the presence of methylene blue. Amitriptyline, 7,8-dioxochlorpromazine and acridine orange were effective inhibitors of the conjugal transfer of the resistance plasmid, R-144, whilst methylene blue, chlorpromazine sulphoxide, and imipramine had only slight effects. We were therefore unable to demonstrate a simple correlation between curing ability and inhibition of plasmid transfer amongst the psychoactive drugs tested. A mechanism of plasmid curing by surface action of the drugs is suggested as an alternative to direct intercalation of the drugs into plasmid DNA.

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