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新型芳酰腙和硫代氨基脲铁螯合剂对氯喹耐药和敏感寄生虫具有抗疟活性。

Novel aroylhydrazone and thiosemicarbazone iron chelators with anti-malarial activity against chloroquine-resistant and -sensitive parasites.

作者信息

Walcourt Asikiya, Loyevsky Mark, Lovejoy David B, Gordeuk Victor R, Richardson Des R

机构信息

Center for Sickle Cell Disease, Howard University, 2121 Georgia Avenue, Washington, DC 20060, USA.

出版信息

Int J Biochem Cell Biol. 2004 Mar;36(3):401-7. doi: 10.1016/s1357-2725(03)00248-6.

Abstract

Iron (Fe) is crucial for cellular proliferation, and Fe chelators have shown activity at preventing the growth of the malarial parasite in cell culture and in animal and human studies. We investigated the anti-malarial activity of novel aroylhydrazone and thiosemicarbazone Fe chelators that show high activity at inhibiting the growth of tumour cells in cell culture [Blood 100 (2002) 666]. Experiments with the chelators were performed using the chloroquine-sensitive, 3D7, and chloroquine-resistant, 7G8, strains of Plasmodium falciparum in vitro. The new ligands were significantly more active in both strains than the Fe chelator in widespread clinical use, desferrioxamine (DFO). The most effective chelators examined were 2-hydroxy-1-naphthylaldehyde isonicotinoyl hydrazone and 2-hydroxy-1-naphthylaldehyde-4-phenyl-3-thiosemicarbazone. The anti-malarial activity correlates with anti-proliferative activity against neoplastic cells demonstrated in a previous study. Our studies suggest that this class of lipophilic chelators may have potential as useful agents for the treatment of malaria.

摘要

铁(Fe)对细胞增殖至关重要,并且铁螯合剂在细胞培养以及动物和人体研究中已显示出抑制疟原虫生长的活性。我们研究了新型芳酰腙和硫代氨基脲铁螯合剂的抗疟活性,这些螯合剂在细胞培养中对肿瘤细胞的生长具有高抑制活性[《血液》100(2002)666]。使用氯喹敏感的3D7株和氯喹耐药的7G8株恶性疟原虫在体外进行了螯合剂实验。在这两种菌株中,新配体的活性均明显高于临床广泛使用的铁螯合剂去铁胺(DFO)。所检测的最有效的螯合剂是2-羟基-1-萘甲醛异烟酰腙和2-羟基-1-萘甲醛-4-苯基-3-硫代氨基脲。抗疟活性与先前研究中证明的对肿瘤细胞的抗增殖活性相关。我们的研究表明,这类亲脂性螯合剂可能具有作为治疗疟疾有用药物的潜力。

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