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多胺生物合成途径抑制剂与已知抗疟药物氯喹对恶性疟原虫的联合作用。

Combined action of inhibitors of polyamine biosynthetic pathway with a known antimalarial drug chloroquine on Plasmodium falciparum.

作者信息

Das B, Gupta R, Madhubala R

机构信息

School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.

出版信息

Pharmacol Res. 1995 Mar-Apr;31(3-4):189-93. doi: 10.1016/1043-6618(95)80017-4.

Abstract

Difluoromethylornithine (alpha-DFMO), a specific enzyme activated inhibitor of ornithine decarboxylase activity, a bis (benzyl) polyamine analogue (MDL 27695) and chloroquine resulted in a dose-dependent inhibition of the parasite. The IC50 value of alpha-DFMO, MDL 27695 and chloroquine was 1.85 mM, 2.0 microM and 23 ng ml-1 respectively. The combined action of MDL 27695 (3 microM) and chloroquine (5 ng ml-1) on P. falciparum growth showed near additive effect, whereas the combination of alpha-DFMO (1.0 mM) and chloroquine (5 ng ml-1) was more than the effect of each drug individually but not additive. Similarly the combined effect of MDL 27695 (3 microM) and alpha-DFMO (1.0 mM) on P. falciparum growth was not additive. The effect of these inhibitors alone and in combination on polyamine biosynthesis is also reported.

摘要

二氟甲基鸟氨酸(α-DFMO),一种鸟氨酸脱羧酶活性的特异性酶激活抑制剂、一种双(苄基)多胺类似物(MDL 27695)以及氯喹对疟原虫产生了剂量依赖性抑制作用。α-DFMO、MDL 27695和氯喹的半数抑制浓度(IC50)值分别为1.85毫摩尔、2.0微摩尔和23纳克/毫升。MDL 27695(3微摩尔)和氯喹(5纳克/毫升)对恶性疟原虫生长的联合作用显示出近似相加效应,而α-DFMO(1.0毫摩尔)和氯喹(5纳克/毫升)的联合作用大于每种药物单独的作用,但并非相加效应。同样,MDL 27695(3微摩尔)和α-DFMO(1.0毫摩尔)对恶性疟原虫生长的联合作用也不是相加的。还报道了这些抑制剂单独及联合使用对多胺生物合成的影响。

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