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有机碲化合物对恰加斯锥虫(Leishmania)的体外和体内活性。

In vitro and in vivo activity of an organic tellurium compound on Leishmania (Leishmania) chagasi.

机构信息

Departamento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina-Universidade Federal de São Paulo, São Paulo, São Paulo, Brazil.

出版信息

PLoS One. 2012;7(11):e48780. doi: 10.1371/journal.pone.0048780. Epub 2012 Nov 7.

Abstract

Tellurium compounds have shown several biological properties and recently the leishmanicidal effect of one organotellurane was demonstrated. These findings led us to test the effect of the organotellurium compound RF07 on Leishmania (Leishmania) chagasi, the agent of visceral leishmaniasis in Latin America. In vitro assays were performed in L. (L.) chagasi-infected bone marrow derived macrophages treated with different concentrations of RF07. In in vivo experiments Golden hamsters were infected with L. (L.) chagasi and injected intraperitoneally with RF07 whereas control animals received either Glucantime or PBS. The effect of RF07 on cathepsin B activity of L. (L.) chagasi amastigotes was assayed spectrofluorometrically using fluorogenic substrates. The main findings were: 1) RF07 showed significant leishmanicidal activity against intracellular parasites at submicromolar concentrations (IC50 of 529.7±26.5 nM), and the drug displayed 10-fold less toxicity to macrophages (CC50 of 5,426±272.8 nM); 2) kinetics assays showed an increasing leishmanicidal action of RF07 at longer periods of treatment; 3) one month after intraperitoneal injection of RF07 L. (L.) chagasi-infected hamsters showed a reduction of 99.6% of parasite burden when compared to controls that received PBS; 4) RF07 inhibited the cathepsin B activity of L. (L.) chagasi amastigotes. The present results demonstrated that the tellurium compound RF07 is able to destroy L. (L.) chagasi in vitro and in vivo at concentrations that are non toxic to the host. We believe these findings support further study of the potential of RF07 as a possible alternative for the chemotherapy of visceral leishmaniasis.

摘要

碲化合物已显示出多种生物学特性,最近证明了一种有机碲化合物对利什曼原虫的杀利什曼原虫作用。这些发现促使我们测试有机碲化合物 RF07 对导致拉丁美洲内脏利什曼病的利什曼原虫(利什曼原虫)chagasi 的影响。在体外试验中,在骨髓来源的巨噬细胞中用不同浓度的 RF07 处理感染 L.(L.)chagasi 的巨噬细胞。在体内实验中,用 L.(L.)chagasi 感染金黄地鼠,并腹膜内注射 RF07,而对照动物接受葡萄糖胺或 PBS。使用荧光底物通过荧光分光光度法测定 RF07 对 L.(L.)chagasi 无鞭毛体中组织蛋白酶 B 活性的影响。主要发现是:1)RF07 在亚微摩尔浓度下对细胞内寄生虫表现出显著的杀利什曼原虫活性(IC50 为 529.7±26.5 nM),并且该药物对巨噬细胞的毒性低 10 倍(CC50 为 5,426±272.8 nM);2)动力学试验表明,随着治疗时间的延长,RF07 的杀利什曼原虫作用逐渐增强;3)与接受 PBS 的对照组相比,腹腔注射 RF07 一个月后,感染 L.(L.)chagasi 的金黄地鼠的寄生虫负担减少了 99.6%;4)RF07 抑制 L.(L.)chagasi 无鞭毛体的组织蛋白酶 B 活性。本研究结果表明,在对宿主无毒的浓度下,碲化合物 RF07 能够在体外和体内破坏 L.(L.)chagasi。我们相信这些发现支持进一步研究 RF07 作为治疗内脏利什曼病的潜在替代药物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e6/3492430/48ccb4b87036/pone.0048780.g001.jpg

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