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朱罗可托因,一种来自克罗顿pullei 变种 glabrior 的戊二酰亚胺生物碱,对利什曼原虫(L.)amazonensis 的活性。

Activity of the julocrotine, a glutarimide alkaloid from Croton pullei var. glabrior, on Leishmania (L.) amazonensis.

机构信息

Laboratório de Parasitologia e Biologia Estrutural, Instituto de Ciências Biológicas, Universidade Federal do Pará, Av. Augusto Corrêa no.01, Bairro Guamá, 66075-110 Belém, Pará, Brazil.

出版信息

Parasitol Res. 2010 Oct;107(5):1075-81. doi: 10.1007/s00436-010-1973-0. Epub 2010 Jul 27.

Abstract

The antiproliferative effect of julocrotine, an alkaloid isolated from Croton pullei var. glabrior (Euphorbiaceae), was studied in the macrophage amastigote and promastigote stages of the protozoan Leishmania (L.) amazonensis, which causes cutaneous leishmaniasis in the New World. Julocrotine showed a dose-dependent effect against the amastigote and promastigote forms, where 79 μM julocrotine inhibited promastigote growth by 54%, with an IC50 of 67 μM. To analyze the antiamastigote activity of the drug, murine peritoneal macrophages infected with L. amazonensis promastigotes were treated with different concentrations of julocrotine. An 80% inhibition of amastigote development was observed using 79 μM julocrotine for 72 h, with an IC50 of 19.8 μM. In addition, ultrastructural observation of the parasites showed a significant reduction in the number of amastigotes in the parasitophorous vacuoles and morphological changes in promastigotes, such as swelling of the mitochondrion, chromatin condensation, presence of membranous structures near the Golgi complex, and some vesicle bodies in the flagellar pocket. A colorimetric assay (MTT), which measures cytotoxic metabolic activity, showed that macrophages maintain their viability after treatment with the drug. These results suggest that julocrotine effectively inhibits the growth of parasites and does not have any cytototoxic effects on the host cell.

摘要

从大籽柳(大戟科)中分离得到的生物碱朱罗卡林(julocrotine)对引起新世界皮肤利什曼病的原生动物利什曼原虫(Leishmania)(L.)亚马逊亚种的巨噬细胞内变形体和前鞭毛体阶段具有抗增殖作用。朱罗卡林对前鞭毛体和内变形体形式表现出剂量依赖性作用,其中 79μM 朱罗卡林抑制前鞭毛体生长 54%,IC50 为 67μM。为了分析药物的抗内变形体活性,用不同浓度的朱罗卡林处理感染 L.亚马逊亚种前鞭毛体的鼠腹腔巨噬细胞。用 79μM 朱罗卡林处理 72h 可观察到 80%的内变形体发育被抑制,IC50 为 19.8μM。此外,对寄生虫的超微结构观察显示,寄生空泡中内变形体的数量显著减少,前鞭毛体的形态发生变化,如线粒体肿胀、染色质浓缩、高尔基体附近存在膜结构以及鞭毛囊中存在一些囊泡体。一种测量细胞毒性代谢活性的比色法(MTT)显示,在用药物处理后,巨噬细胞保持其活力。这些结果表明,朱罗卡林能有效抑制寄生虫的生长,且对宿主细胞没有任何细胞毒性作用。

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