Muchtar Nur Hazirah, Nik Mat Zin Nik Nor Imam, Mohamad Fatin Sofia, Abu-Bakar Nurhidanatasha
School of Health Sciences, Universiti Sains Malaysia, Kelantan, Malaysia.
Malays J Med Sci. 2022 Aug;29(4):43-52. doi: 10.21315/mjms2022.29.4.5. Epub 2022 Aug 29.
Malaria is one of the leading causes of death worldwide caused by parasites of the genus . The reduced efficacy of the mainstay antimalarial drugs due to the widespread of drug-resistant () necessitates an effort to develop novel antimalarial drugs with new targets. The effects of a phenolic compound, ellagic acid, against the malaria parasite have previously been reported. This present study aimed to evaluate the effect of ellagic acid on pH of the digestive vacuole.
The antimalarial potential of ellagic acid against the chloroquine-sensitive strain (3D7) of was assessed by using a malarial SYBR Green 1 fluorescence-based (MSF) assay. The effect of different concentrations of ellagic acid on the pH of the parasite's digestive vacuole at mid-trophozoite stage was examined by using a ratiometric pH indicator, fluorescein isothiocyanate (FITC)-dextran on the flow cytometry.
The result of the MSF assay showed that ellagic acid has an antimalarial activity (half-maximal inhibitory concentration [IC] = 1.85 ± 4.57 nM) at par with a standard drug, artemisinin (IC = 1.91 ± 5.41 nM). The pH of the digestive vacuole of ellagic acid-treated parasites was significantly changed (pH values ranged from 6.11 to 6.74) in a concentration-dependent manner as compared to untreated parasites ( < 0.001). A similar effect was shown by the parasites treated with a standard proton pump inhibitor, concanamycin A.
These findings suggest that ellagic acid might have altered the digestive vacuole pH through the inhibition of proton pumps that regulate the acidification of this organelle. Overall, this study provides a valuable insight into the potential of ellagic acid as a promising antimalarial candidate with a novel mechanism of action.
疟疾是由疟原虫属寄生虫引起的全球主要死因之一。由于耐药疟原虫的广泛传播,主要抗疟药物的疗效降低,因此有必要努力开发具有新靶点的新型抗疟药物。此前已有报道一种酚类化合物鞣花酸对疟原虫的作用。本研究旨在评估鞣花酸对消化液泡pH值的影响。
通过基于疟原虫SYBR Green 1荧光的(MSF)测定法评估鞣花酸对氯喹敏感株(3D7)疟原虫的抗疟潜力。在流式细胞仪上使用比例pH指示剂异硫氰酸荧光素(FITC)-葡聚糖检测不同浓度的鞣花酸对滋养体中期疟原虫消化液泡pH值的影响。
MSF测定结果表明,鞣花酸具有抗疟活性(半数最大抑制浓度[IC]=1.85±4.57 nM),与标准药物青蒿素(IC=1.91±5.41 nM)相当。与未处理的疟原虫相比,经鞣花酸处理的疟原虫消化液泡的pH值以浓度依赖性方式显著变化(pH值范围为6.11至6.74)(P<0.001)。用标准质子泵抑制剂 concanamycin A处理的疟原虫也显示出类似的效果。
这些发现表明,鞣花酸可能通过抑制调节该细胞器酸化的质子泵改变了消化液泡的pH值。总体而言,本研究为鞣花酸作为一种具有新作用机制的有前景的抗疟候选药物的潜力提供了有价值的见解。