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猫头鹰猴(三带夜猴)体内的恶性疟原虫和间日疟原虫感染。III. 寻找新型血液裂殖体杀灭药物所采用的方法。

Plasmodium falciparum and Plasmodium vivax infections in the owl monkey (Aotus trivirgatus). III. Methods employed in the search for new blood schizonticidal drugs.

作者信息

Schmidt L H

出版信息

Am J Trop Med Hyg. 1978 Jul;27(4):718-37. doi: 10.4269/ajtmh.1978.27.718.

DOI:10.4269/ajtmh.1978.27.718
PMID:99057
Abstract

This report describes, illustrates, and validates the major features of a procedure designed to provide primary assessments of the activities of potential antimalarial drugs against infections with chloroquine-resistant or pyrimethamine-resistant strains of Plasmodium falciparum in owl monkeys of Colombian origin. Studies with 14 specially selected compounds have shown that the test method has the capacity to identify and quantify diverse levels of therapeutic efficacy among agents that differ widely in chemical structure. Extended studies with two of the above compounds indicate that such assessments have an acceptable level of reproducibility. Experiments with two other agents, structurally different from those in the selected group, have shown that the impacts of pyrimethamine resistance (or chloroquine resistance) on the activity of a compound can be readily identified during routine application of the test procedure, as can emergence of parasites resistant to the test agent. The above body of information can usually be acquired in infections with two strains of P. falciparum, one chloroquine-resistant, the other pyrimethamine-resistant, with commitments of no more than 1.5 g of test compound and 12 owl monkeys. These modest requirements have made it possible to utilize human plasmodial infections in the owl monkey in the search for new blood schizonticidal drugs more broadly effective than those currently available.

摘要

本报告描述、阐释并验证了一种程序的主要特征,该程序旨在对潜在抗疟药物针对哥伦比亚原产夜猴体内耐氯喹或耐乙胺嘧啶恶性疟原虫感染的活性进行初步评估。对14种特别挑选的化合物进行的研究表明,该测试方法有能力识别和量化化学结构差异很大的药物之间不同水平的治疗效果。对上述两种化合物的进一步研究表明,此类评估具有可接受的重现性水平。对另外两种结构与所选组不同的药物进行的实验表明,在测试程序的常规应用过程中,可以很容易地识别乙胺嘧啶耐药性(或氯喹耐药性)对化合物活性的影响,以及对测试药物产生耐药性的寄生虫的出现情况。上述信息通常可以通过感染两种恶性疟原虫菌株获得,一种耐氯喹,另一种耐乙胺嘧啶,测试化合物用量不超过1.5克,夜猴数量不超过12只。这些适度的要求使得利用夜猴体内的人体疟原虫感染来寻找比现有药物更具广泛疗效的新型血内裂殖体杀灭药物成为可能。

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