Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
Antimicrob Agents Chemother. 2012 Nov;56(11):5774-81. doi: 10.1128/AAC.00873-12. Epub 2012 Aug 27.
The current treatment of visceral leishmaniasis is made difficult by the low efficacy, elevated costs, low bioavailability, and high toxicity of many of the available drugs. Primaquine, an antimalarial 8-aminoquinoline, displays activity against Leishmania spp., and several of its derivatives have been developed as potential antileishmanial drugs. However, primaquine exhibits low oral bioavailability due to oxidative deamination of its aliphatic chain. We previously developed peptidomimetic and organometallic derivatives of primaquine, with higher resistance to proteolytic degradation and oxidative deamination, which presented significant activity against primaquine-sensitive pathogens such as Plasmodium or Pneumocystis. In light of these relevant findings, we decided to evaluate these compounds against both the promastigote and intramacrophagic amastigote forms of Leishmania infantum, the agent of Mediterranean visceral leishmaniasis. We found that several of these compounds had significant activity against L. infantum. One of the peptidomimetic (3c) and one of the organometallic (7a) derivatives of primaquine were active against the clinically relevant intramacrophagic amastigote form of the parasite, causing >96% reductions in the number of amastigotes per 100 macrophages at 60 and 40 μM, respectively, while being less cytotoxic for host cells than the reference drugs sitamaquine and miltefosine. Hence, compounds 3c and 7a represent new entries toward the development of new antileishmanial leads.
目前,许多可用药物的疗效低、成本高、生物利用度低和毒性高,使得内脏利什曼病的治疗变得困难。普那喹啉是一种抗疟 8-氨基喹啉,对利什曼原虫属显示出活性,其几种衍生物已被开发为潜在的抗利什曼病药物。然而,由于其脂肪链的氧化脱氨作用,普那喹啉表现出低的口服生物利用度。我们之前开发了普那喹啉的肽模拟物和有机金属衍生物,它们对蛋白水解降解和氧化脱氨具有更高的抗性,对普那喹啉敏感的病原体如疟原虫或卡氏肺孢子虫具有显著的活性。鉴于这些相关发现,我们决定评估这些化合物对利什曼原虫婴儿期的前鞭毛体和巨噬细胞内无鞭毛体形式的活性。我们发现,这些化合物中的几种对 L. infantum 具有显著的活性。普那喹啉的一种肽模拟物(3c)和一种有机金属衍生物(7a)对寄生虫的临床相关巨噬细胞内无鞭毛体形式具有活性,在 60 和 40 μM 时分别导致每 100 个巨噬细胞中的无鞭毛体数量减少>96%,而对宿主细胞的细胞毒性低于参考药物司他喹啉和米替福新。因此,化合物 3c 和 7a 代表了开发新的抗利什曼病先导化合物的新进展。