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Assessment of causal prophylactic activity in Plasmodium berghei yoelii and its value for the development of new antimalarial drugs

机译:伯氏疟原虫的因果预防活性评估及其对开发抗疟新药的价值

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摘要

The causal prophylactic activity of several reference and experimental antimalarial compounds was assessed in sporozoite-induced infections of NMRI mice with Plasmodium berghei yoelii (strain 17X). The animals were inoculated with 10 000 sporozoites per mouse and treated once 2-4 hours later. The test system has proved to be very suitable in experiments involving more than 3 000 mice. The infection rate in 448 untreated controls was 97.3%. Lowering the sporozoite content of the inoculum to 1 000 or 100 sporozoites markedly reduced the rate (65.1% and 32.7%). In experiments with primaquine the causal prophylactic activity was also influenced by the time of drug administration before or after sporozoite inoculation. No causal prophylactic effect was demonstrable with quinine, chloroquine, amodiaquine, amopyroquine, RC-12, or B 505. Primaquine was active, but pamaquine and pentaquine were only sporadically active. The pre-erythrocytic stages of P. b. yoelii were only slightly sensitive to dapsone, sulfadiazine, and sulformethoxine; they were 10-100 times more susceptible to proguanil, cycloguanil, and pyrimethamine. The experimental 6-aminoquinolines NI 147/36, NI 187/82, and BA 138/111 and the 7-chlorolincomycin derivative U 24729 were also studied. Experiments in which curative activity against blood-induced infections of P. b. yoelii was evaluated showed that the causal prophylactics act more specifically against the pre-erythrocytic than against the erythrocytic forms. This specificity was most pronounced among the DHFR-inhibitors, whose outstanding activity may be explained by the fact that the rate of multiplication of the pre-erythrocytic forms of P. b. yoelii is greater than that of other plasmodia used hitherto; it is also greater than the rate shown by the malaria parasites of man and that of the erythrocytic forms of P. b. yoelii itself. We believe that this feature will render P. b. yoelii very useful for determination of the causal prophylactic activity of new compounds, but it may also overrate the potency of drugs that interfere with nucleic acid biosynthesis.
机译:在子孢子诱发的伯氏疟原虫(17X株)对NMRI小鼠的子孢子诱导的感染中,评估了几种参考和实验抗疟化合物的因果预防活性。每只小鼠用10000只子孢子接种动物,并在2-4小时后处理一次。该测试系统已被证明非常适合涉及3000多只小鼠的实验。 448名未经治疗的对照组的感染率为97.3%。将接种物中的子孢子含量降低到1000或100时,子孢子率显着降低(分别为65.1%和32.7%)。在使用伯氨喹的实验中,因子孢子接种之前或之后的给药时间也影响了因果预防活性。奎宁,氯喹,阿莫地喹,阿莫吡喹,RC-12或B 505均未显示因果预防作用。伯氨喹是有活性的,但pamaquine和五喹是偶发性的。 P. b。的前红细胞生成阶段。约埃利对氨苯砜,磺胺嘧啶和次硫酸甲氧嘧啶只稍敏感。他们对鸟嘌呤,环鸟嘌呤和乙胺嘧啶的敏感度高10-100倍。还研究了实验性6-氨基喹啉NI 147/36,NI 187/82和BA 138/111以及7-氯林可霉素衍生物U 24729。对抗血液诱导的P.b.感染的治愈活性的实验。 yoelii被评估显示,因果性预防措施对前红细胞生成的作用比对前红细胞生成的作用更具体。这种特异性在DHFR抑制剂中最为明显,其突出的活性可以通过P.b的促红细胞前形式的增殖速率这一事实来解释。 yoelii大于迄今使用的其他疟原虫;它也大于人的疟疾寄生虫和P. b的红细胞形式所显示的比率。 yoelii本身。我们认为此功能将渲染P。 yoelii对于确定新化合物的因果预防活性非常有用,但它也可能高估了干扰核酸生物合成的药物的效力。

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