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锥虫杀灭和 20-去氧沙利霉素的细胞肿胀活性。

Trypanocidal and cell swelling activity of 20-deoxysalinomycin.

机构信息

Bob Champion Research & Education Building, Norwich Medical School, University of East Anglia, Norwich, UK.

Centre for Analysis and Synthesis, Department of Chemistry, Lund University, Lund, Sweden.

出版信息

Exp Parasitol. 2022 Dec;243:108414. doi: 10.1016/j.exppara.2022.108414. Epub 2022 Oct 21.

Abstract

The naturally occurring polyether ionophore salinomycin was previously found to display promising anti-proliferative activity against bloodstream forms of Trypanosoma brucei. Here, we report the evaluation of 20-deoxysalinomycin, a naturally occurring homolog to salinomycin, for trypanocidal and cell swelling activity. The concentration of 20-deoxysalinomycin required to reduce the growth rate of bloodstream-form trypanosomes by 50% was determined to be 0.12 μM and found to be 8 times more trypanocidal than that of salinomycin. Moreover, 20-deoxysalinomycin and salinomycin displayed similar cytotoxic activity against human HL-60 cells. Measured as the ratio of cytotoxic to trypanocidal activity, 20-deoxysalinomycin thus exhibits a four-fold higher selectivity compared to salinomycin. The stronger trypanocidal activity of 20-deoxysalinomycin is attributed to an enhanced ability to induce cell swelling in trypanosomes. The findings support 20-deoxysalinomycin as a useful lead in the rational development of new and improved anti-trypanosomal drugs.

摘要

先前发现天然聚醚离子载体萨利霉素对布氏锥虫血腔形式具有有前景的抗增殖活性。在这里,我们报告了对 20-去氧萨利霉素(萨利霉素的天然同系物)的评估,用于杀锥虫和细胞肿胀活性。确定使血腔型锥虫的生长速率降低 50%所需的 20-去氧萨利霉素的浓度为 0.12μM,并且发现其杀锥虫活性比萨利霉素高 8 倍。此外,20-去氧萨利霉素和萨利霉素对人 HL-60 细胞表现出相似的细胞毒性活性。以细胞毒性与杀锥虫活性的比率来衡量,20-去氧萨利霉素的选择性比萨利霉素高四倍。20-去氧萨利霉素更强的杀锥虫活性归因于增强了诱导锥虫细胞肿胀的能力。这些发现支持 20-去氧萨利霉素作为合理开发新型和改良抗锥虫药物的有用先导物。

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