竹属药用植物化学物质抗疟原虫活性及抑制脂质过氧化和寄生虫血红素聚合活性的评价

Q4 Immunology and Microbiology
I. Onyesom, C. Elu, J. Acha, E. Ojugbeli, E.P. Ochonogor, L.O. Udumebraye
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引用次数: 0

摘要

尽管为消除疟疾进行了不懈的努力,但由于无数因素导致的控制和治疗方法失败,目前的感染趋势,特别是在撒哈拉以南非洲,仍然令人担忧。因此,寻找新的、负担得起的、更有效的抗疟疾药物,特别是从植物中提取的药物,已成为近年来的前沿工作。因此,本研究采用文献记录的方法,评价了毛茛的植物化学成分(生物碱、黄酮类、单宁、皂苷、心苷和蒽醌)提取物的体外抗质体、细胞毒和抗氧化活性。采用寄生虫生长抑制法测定其抗疟原虫活性,乳酸脱氢酶法测定其细胞毒活性。通过测定提取物对脂质过氧化和热聚合的抑制作用来测定其抗氧化活性。结果表明,该生物碱提取物无细胞毒性(CC = 60.26 μg/mL),选择性最强(SI = 125.5),抗疟原虫活性最高(IC = 0.48 μg/mL),抑制血红素聚合活性最高(IC = 0.63 μg/mL),抗脂质过氧化抑制作用中等(LPI;50 IC = 500μg/mL)容量。其中,乙醇提取物和黄酮类提取物在抑制热聚合(IC = 0.46 μg/mL)和脂质过氧化(IC = 218.78 μg/mL)方面的抗氧化活性最高,在抗疟原虫活性(IC = 0.48 μg/mL和1.10 μg/mL)方面的抗氧化活性最高。我们的研究结果表明,所有50种植物化学提取物均无细胞毒性。虽然黄酮类和乙醇类植物化学提取物的抗氧化活性高于生物碱类植物化学提取物,但生物碱是柽柳抗疟原虫活性最强的植物化学物质,其作用机制之一是抑制寄生虫血红素的解毒作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of antiplasmodial activity and inhibitions of lipid peroxidation and parasite haem polymerization activity by medicinal phytochemicals of Phyllanthus amarus
Despite the dedicated struggle to eliminate malaria, the current trend of the infection, particularly, in sub-Saharan Africa remains worrisome due to failing control and treatment approaches caused by a myriad of factors. Therefore, the search for new, affordable, and more potent antimalarial drugs, from plants especially, have become the frontline in recent times. This study thus, evaluates the in vitro antiplasmodial, cytotoxic and antioxidant activities of the phytochemical (alkaloids, flavonoids, tannins, saponins, cardiac glycosides and anthraquinones) extracts of Phyllanthus amarus using documented methods. Antiplasmodial and cytotoxic activities were determined by parasite growth inhibition assay and microassay technique by the lactate dehydrogenase method, respectively. Antioxidant activities were determined by measuring inhibition of both lipid peroxidation and heam polymerization by extracts. Results show that the alkaloid extract was noncytotoxic (CC = 60.26 μg/mL) and most selectable (SI = 125.5) with the highest antiplasmodial (IC = 0.48 μg/mL) and 50 50 haem polymerization inhibition (IC = 0.63 μg/mL) activities, but moderate antioxidant lipid peroxidation inhibition, (LPI; 50 IC = 500μg/mL) capacity. However, the ethanol and flavonoid phytochemical extracts displayed the highest antioxidant 50 activity in inhibition of heam polymerization (IC = 0.46 μg/mL) and lipid peroxidation (IC = 218.78 μg/mL), respectively, 50 50 with significant antiplasmodial activity (IC = 0.48 μg/mL and 1.10 μg/mL, respectively). Our results show that all 50s phytochemical extracts studied were non-cytotoxic. Although the antioxidant activities of the flavonoid and ethanol phytochemical extracts were greater in comparison to the alkaloid phytochemical, alkaloid was the most selectable active antiplasmodial phytochemical of P. amarus and one of its mechanisms of action is by inhibiting parasite haem detoxification.
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来源期刊
Nigerian Journal of Parasitology
Nigerian Journal of Parasitology Medicine-Infectious Diseases
CiteScore
0.20
自引率
0.00%
发文量
43
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