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卡氏肺孢子虫的多胺含量及对鸟氨酸脱羧酶抑制剂DL-α-二氟甲基鸟氨酸的反应

Polyamine content of Pneumocystis carinii and response to the ornithine decarboxylase inhibitor DL-alpha-difluoromethylornithine.

作者信息

Merali S, Clarkson A B

机构信息

Department of Medical and Molecular Parasitology, New York University School of Medicine, New York 10016, USA.

出版信息

Antimicrob Agents Chemother. 1996 Apr;40(4):973-8. doi: 10.1128/AAC.40.4.973.

Abstract

Difluoromethylornithine (DFMO; eflornithine hydrochloride [Ornidyl]), a suicide inhibitor of the key polyamine biosynthesis enzyme ornithine decarboxylase (ODC), is effective in treating Pneumocystis carinii pneumonia, a common opportunistic infection associated with AIDS. Despite DFMO's specificity for ODC, the reason for its selective toxicity against P. carinii is unknown since both host and parasite are dependent on the same enzyme for polyamine biosynthesis. A new high-performance liquid chromatography method was used with P. carinii cells isolated from infected rat lungs to measure polyamine content, to confirm the presence of ODC, and to examine the effect of DFMO on polyamine concentrations. Putrescine, spermidine, and spermine were found to be present at 2.00 +/- 0.54, 1.26 +/- 0.51, and 1.59 +/- 0.91 nmol (mg of protein)-1, respectively, neither unusually high nor low values. ODC's specific activity was 79 +/- 11 pmol (mg of protein)-1 h-1, again not a remarkable value. However, the rates of both DFMO-induced polyamine depletion and subsequent repletion upon DFMO removal were unusually high. A 3-h exposure to 1 mM DFMO in vitro caused the depletion of putrescine, spermidine, and spermine to levels 12, 29, and 16%, respectively, of that of control cells. After DFMO removal and incubation for 1 h in serum-free media, polyamine levels returned to 78, 88, and 64%, respectively, of that of the control cells not exposed to DFMO. Since such depletions and repletions usually occur over periods of days rather than hours, these rapid changes may provide a clue to the selective action of DFMO against P. carinii and may guide the development of new compounds and an optimal drug administration schedule for DFMO.

摘要

二氟甲基鸟氨酸(DFMO;盐酸依氟鸟氨酸[奥尼地])是关键多胺生物合成酶鸟氨酸脱羧酶(ODC)的自杀性抑制剂,对治疗卡氏肺孢子虫肺炎有效,这是一种与艾滋病相关的常见机会性感染。尽管DFMO对ODC具有特异性,但其对卡氏肺孢子虫的选择性毒性原因尚不清楚,因为宿主和寄生虫在多胺生物合成中都依赖于同一种酶。一种新的高效液相色谱法用于检测从感染大鼠肺中分离出的卡氏肺孢子虫细胞的多胺含量,以确认ODC的存在,并研究DFMO对多胺浓度的影响。腐胺、亚精胺和精胺的含量分别为2.00±0.54、1.26±0.51和1.59±0.91 nmol/(mg蛋白质)-1,既不异常高也不异常低。ODC的比活性为79±11 pmol/(mg蛋白质)-1 h-1,同样不是一个显著的值。然而,DFMO诱导的多胺消耗速率以及去除DFMO后的后续补充速率异常高。在体外暴露于1 mM DFMO 3小时后,腐胺、亚精胺和精胺的水平分别降至对照细胞的12%、29%和16%。去除DFMO并在无血清培养基中孵育1小时后,多胺水平分别恢复到未暴露于DFMO的对照细胞的78%、88%和64%。由于这种消耗和补充通常发生在数天而非数小时内,这些快速变化可能为DFMO对卡氏肺孢子虫的选择性作用提供线索,并可能指导新化合物的开发以及DFMO的最佳给药方案。

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