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布氏布氏锥虫对乙酰氨基阿苯达唑(贝尼尔)的时间-剂量反应以及牛血浆中药物浓度-时间曲线的体外模拟

Time-dose-response of Trypanosoma brucei brucei to diminazene aceturate (Berenil) and in vitro simulation of drug-concentration-time profiles in cattle plasma.

作者信息

Kaminsky R, Mamman M, Chuma F, Zweygarth E

机构信息

International Laboratory for Research on Animal Diseases (ILRAD), Nairobi, Kenya.

出版信息

Acta Trop. 1993 Jun;54(1):19-30. doi: 10.1016/0001-706x(93)90065-j.

Abstract

Bloodstream form Trypanosoma brucei brucei of axenically growing populations were incubated in the presence of 10.0, 1.0 or 0.1 micrograms/ml diminazene aceturate (Berenil) at 37 degrees C for various periods and, subsequently, either inoculated into mice or further propagated in vitro in drug-free medium. Growth was monitored for 10 days. The ability of trypanosomes of drug-sensitive CP 2137 (clone 1) to grow in vitro was irreversibly damaged after short incubation (< 1 min) with 10.0 micrograms/ml or after 15 min with 1.0 micrograms/ml diminazene aceturate. In contrast, drug-resistant CP 2469 (clone 1) trypanosomes tolerated incubation with 10 micrograms/ml of drug for up to 6 h and 1.0 micrograms/ml of drug for up to 24 h. Differences in drug susceptibility were also detected regarding infectivity to mice and changes in trypanosome cell volume. The results demonstrated that less than 1 min exposure to diminazene aceturate at concentrations as seen in bovine plasma at the initial peak after diminazene aceturate treatment is enough to irreversibly damage drug-sensitive trypanosomes. However, these concentrations were not sufficient to completely eliminate drug-resistant trypanosomes after exposure for 1-6 h; trypanosomes continued to grow for 48 h before the majority of them died and only a few organisms survived to revive the cultures. When drug-sensitive trypanosomes were exposed in vitro for 24 h to diminazene aceturate at the level of concentrations found in cattle after treatment with 3.5 mg/kg, most of the trypanosomes died and none of the surviving parasites could be propagated in vitro in the absence of drug for more than 2 days. However, a small population of drug-resistant trypanosomes was not irreversibly damaged and a few surviving trypanosomes were able to establish growing cultures. The addition of feeder layer cells did not change the outcome of these experiments.

摘要

将在无共生环境中生长的群体的布氏布氏锥虫血流型在37℃下于10.0、1.0或0.1微克/毫升的乙酰氨基阿苯达唑(贝尼尔)存在下孵育不同时间,随后,要么接种到小鼠体内,要么在无药物培养基中进一步体外培养。监测生长10天。药物敏感的CP 2137(克隆1)锥虫在与10.0微克/毫升孵育短时间(<1分钟)后或与1.0微克/毫升乙酰氨基阿苯达唑孵育15分钟后,其体外生长能力受到不可逆损害。相比之下,耐药的CP 2469(克隆1)锥虫能耐受与10微克/毫升药物孵育长达6小时以及与1.0微克/毫升药物孵育长达24小时。在对小鼠的感染性和锥虫细胞体积变化方面也检测到了药物敏感性差异。结果表明,在乙酰氨基阿苯达唑治疗后的初始峰值时,暴露于牛血浆中所见浓度的乙酰氨基阿苯达唑不到1分钟就足以不可逆地损害药物敏感的锥虫。然而,这些浓度在暴露1 - 6小时后不足以完全消除耐药锥虫;锥虫在大多数死亡之前继续生长48小时,只有少数生物体存活下来使培养物复苏。当药物敏感的锥虫在体外暴露于3.5毫克/千克治疗后牛体内发现的浓度水平的乙酰氨基阿苯达唑24小时时,大多数锥虫死亡,在无药物的情况下,存活的寄生虫没有一个能在体外繁殖超过2天。然而,一小部分耐药锥虫没有受到不可逆损害,少数存活的锥虫能够建立生长的培养物。添加饲养层细胞并没有改变这些实验的结果。

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