Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, P.O. Box LG 581, Legon, Ghana.
Section of Environmental Parasitology, Faculty of Medicine, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8510, Japan.
Phytother Res. 2018 Aug;32(8):1617-1630. doi: 10.1002/ptr.6093. Epub 2018 May 7.
Trypanosomiasis, leishmaniasis, and malaria are protozoan infections of public health importance with thousands of new cases recorded annually. Control of these infection(s) with existing chemotherapy is limited by drug toxicity, lengthy parenteral treatment, affordability, and/or the emergence of resistant strains. Medicinal plants on the other hand are used in the treatment of various infectious diseases although their chemical properties are not fully evaluated. In this study, we screened 112 crude extracts from 72 selected Ghanaian medicinal plants for anti-Trypanosoma, anti-Leishmania, and anti-Plasmodium activities in vitro and investigated their mechanisms of action. Twenty-three extracts from 20 plants showed significant antiprotozoan activity against at least 1 of 3 protozoan parasites screened with IC values less than 20 μg/ml. Eleven extracts showed high anti-Trypanosoma activity with Bidens pilosa whole plant and Morinda lucida leaf extracts recording the highest activities. Their IC (selectivity index [SI]) values were 5.51 μg/ml (35.00) and 5.96 μg/ml (13.09), respectively. Nine extracts had high anti-Leishmania activity with Annona senegalensis and Cassia alata leaf extracts as the most active. Their IC (SI) values were 10.8 μg/ml (1.50) and 10.1 μg/ml (0.37), respectively. Six extracts had high anti-Plasmodium activity with the leaf and stem-bark extracts of Terminalia ivorensis recording the highest activity. Their IC (SI) values were 7.26 μg/ml (129.36) and 17.45 μg/ml (17.17), respectively. Only M. lucida at 25 μg/ml induced significant apoptosis-like cell death in Trypanosoma parasites. Anti-Leishmania active extracts induced varying morphological changes in Leishmania parasites such as multiple nuclei and/or kinetoplast, incomplete flagella division, or nuclear fragmentation. Active extracts may be potential sources for developing new chemotherapy against these infections.
锥虫病、利什曼病和疟疾是具有公共卫生重要性的原生动物感染,每年都有数千例新病例记录。现有的化疗药物在控制这些感染方面受到药物毒性、长期的静脉治疗、可负担性和/或耐药株出现的限制。另一方面,药用植物用于治疗各种传染病,尽管它们的化学性质尚未完全评估。在这项研究中,我们对 72 种加纳药用植物的 112 种粗提取物进行了筛选,以评估它们对体外的抗锥虫、抗利什曼原虫和抗疟原虫活性,并研究了它们的作用机制。从 20 种植物中提取的 23 种提取物对至少 1 种筛选的 3 种原生动物寄生虫具有显著的抗原生动物活性,其 IC 值小于 20μg/ml。11 种提取物对锥虫具有高活性,其中菊科植物 Bidens pilosa 全草和桃金娘科植物 Morinda lucida 的叶提取物活性最高。它们的 IC(选择性指数 [SI])值分别为 5.51μg/ml(35.00)和 5.96μg/ml(13.09)。9 种提取物对利什曼原虫具有高活性,其中 Annona senegalensis 和 Cassia alata 的叶提取物活性最高。它们的 IC(SI)值分别为 10.8μg/ml(1.50)和 10.1μg/ml(0.37)。6 种提取物对疟原虫具有高活性,其中桃金娘科植物 Terminalia ivorensis 的叶和茎皮提取物活性最高。它们的 IC(SI)值分别为 7.26μg/ml(129.36)和 17.45μg/ml(17.17)。只有 25μg/ml 的 M. lucida 能诱导锥虫寄生虫发生明显的凋亡样细胞死亡。抗利什曼原虫活性提取物能诱导利什曼原虫发生多种形态变化,如多核和/或动基体、不完全鞭毛分裂或核碎裂。活性提取物可能是开发针对这些感染的新化疗药物的潜在来源。