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关于汽巴-嘉基化合物CGP 6140、20376、20309和21833抗盘尾丝虫第三期和第四期幼虫活性的研究。

Studies on the activity of the Ciba Geigy compounds CGP 6140, 20376, 20309 and 21833 against third and fourth stage larvae of Onchocerca volvulus.

作者信息

Strote G

机构信息

Department of Helminthology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, FRG.

出版信息

Trop Med Parasitol. 1989 Mar;40(1):51-6.

PMID:2740728
Abstract

The effect of four new antifilarial compounds, (CGP 6140, 20376, 20309 and 21833, Ciba Geigy Ltd. Basle) on the viability of third and fourth stage larvae of Onchocerca volvulus was tested in vitro and in vivo. The motility of the larval stages and the moulting process from the third to the fourth stage were used as parameters for the drug activity in vitro. All four compounds showed good effects in vitro on the moulting rates compared to the controls after incubation at different concentrations in culture medium with serum. After an exposure for three hours to different concentrations of the compounds in medium without serum, only CGP 20376 had a clear inhibitory effect on the developing larvae. The moulting rate was reduced by this compound to 20% of the control values with 1 microgram/ml, a concentration that is comparable to plasma levels reported from chimpanzees. In both experimental situations, with serum and without serum, the motility of the developing larvae was only affected at very high concentrations of the compounds. The results obtained with fourth stage larvae were comparable. CGP 6140 and CGP 20376 were tested in vivo, using a diffusion chamber technique for the implantation of infective larvae into the peritoneum of Mastomys natalensis and assessing the survival of the implanted parasites. High doses of CGP 6140 had only unsatisfactory effects on the larvae in this model system whereas CGP 20376 had inhibited moulting and killed most larvae with a daily dose of 25 mg/kg for five consecutive days.

摘要

测试了四种新型抗丝虫化合物(CGP 6140、20376、20309和21833,瑞士巴塞尔汽巴 - 嘉基有限公司)对盘尾丝虫第三和第四期幼虫活力的体内和体外作用。幼虫阶段的运动能力以及从第三期到第四期的蜕皮过程被用作体外药物活性的参数。与对照组相比,在含有血清的培养基中以不同浓度孵育后,所有四种化合物在体外对蜕皮率均显示出良好的效果。在无血清培养基中暴露于不同浓度的化合物三小时后,只有CGP 20376对发育中的幼虫有明显的抑制作用。该化合物在1微克/毫升的浓度下将蜕皮率降低至对照值的20%,该浓度与黑猩猩报告的血浆水平相当。在有血清和无血清的两种实验情况下,只有在化合物浓度非常高时,发育中幼虫的运动能力才会受到影响。用第四期幼虫获得的结果类似。使用扩散室技术将感染性幼虫植入南非多乳鼠的腹膜并评估植入寄生虫的存活情况,对CGP 6140和CGP 20376进行了体内测试。在该模型系统中,高剂量的CGP 6140对幼虫的作用仅不尽人意,而CGP 20376连续五天每日剂量为25毫克/千克时,抑制了蜕皮并杀死了大多数幼虫。

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