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芹菜素-7-O-葡萄糖苷与乙胺嘧啶对生长的相互作用。

Interaction of apigenin-7-O-glucoside with pyrimethamine against growth.

作者信息

Abugri Daniel A, Witola William H

机构信息

1Department of Chemistry, Laboratory of Ethnomedicine, Parasitology and Drug Discovery, Tuskegee University, Tuskegee, AL 36088 USA.

2Department of Biology, Tuskegee University, Tuskegee, AL 36088 USA.

出版信息

J Parasit Dis. 2020 Mar;44(1):221-229. doi: 10.1007/s12639-019-01185-5. Epub 2019 Dec 2.

Abstract

Apigenin-7-O-glucoside, a flavonoid glucoside known to inhibit cancer cell growth, fungi growth, both intra and extracellular reactive oxygen species generation, causing cell arrest and damage to the plasma membrane, was tested alone or in combination with a dihydrofolate inhibitor (pyrimethamine) against () growth. The anti- activity was carried out using a high throughput antiparasitic drug screening cell-based assay known as 2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H tetrazolium, monosodium salt (WST-8) and fluorescence plate reader. The 50% effective concentration inhibition and 95% confidence interval values for individual and combination treatments against were 0.80 (0.38-1.29) µg/mL, 1.05 (0.275-2.029) µg/mL, and 0.40 (0-1.06) µg/mL for apigenin-7-O-glucoside, pyrimethamine, and apigenin-7-O-glucoside plus pyrimethamine, respectively. Interestingly, the apigenin-7-O-glucoside plus pyrimethamine combination showed an additive inhibition effect against growth in vitro using the fractional inhibitory concentration index method. It was discovered that the apigenin-7-O-glucoside combination with pyrimethamine had a high selectivity index 62.5, which implies 62-fold inhibition activity against the parasite versus human foreskin fibroblast cell cytotoxicity. This new combination hit is novel and will have the potential for future effective, safe, and less costly anti- drug development, if its in vivo activity shows similar findings.

摘要

芹菜素 -7 -O -葡萄糖苷是一种已知可抑制癌细胞生长、真菌生长、细胞内外活性氧生成、导致细胞停滞并损伤质膜的黄酮类葡萄糖苷,单独或与二氢叶酸抑制剂(乙胺嘧啶)联合用于测试对()生长的抑制作用。抗()活性通过一种基于细胞的高通量抗寄生虫药物筛选试验进行,该试验称为2 -(2 -甲氧基 -4 -硝基苯基)-3 -(4 -硝基苯基)-5 -(2,4 -二磺酸苯基)-2H四唑单钠盐(WST -8)和荧光酶标仪。芹菜素 -7 -O -葡萄糖苷、乙胺嘧啶以及芹菜素 -7 -O -葡萄糖苷加乙胺嘧啶单独及联合处理对()的50%有效浓度抑制值和95%置信区间分别为0.80(0.38 - 1.29)μg/mL、1.05(0.275 - 2.029)μg/mL和0.40(0 - 1.06)μg/mL。有趣的是,使用分数抑制浓度指数法,芹菜素 -7 -O -葡萄糖苷加乙胺嘧啶组合在体外对()生长显示出相加抑制作用。研究发现,芹菜素 -7 -O -葡萄糖苷与乙胺嘧啶的组合具有高选择性指数62.5,这意味着对寄生虫的抑制活性是对人包皮成纤维细胞细胞毒性的62倍。如果其体内活性显示出类似结果,这种新的联合药物是新颖的,并且具有未来开发有效、安全且成本较低的抗()药物的潜力。

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