Sadiq Muhammad Bilal, Tharaphan Pattamon, Chotivanich Kesinee, Tarning Joel, Anal Anil Kumar
Food Engineering and Bioprocess Technology, Asian Institute of Technology, Klongluang, PO Box 4, Bangkok, Pathumthani, 12120, Thailand.
Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
BMC Complement Altern Med. 2017 Jul 18;17(1):372. doi: 10.1186/s12906-017-1878-x.
The emergence of drug resistant malaria is threatening our ability to treat and control malaria in the Southeast Asian region. There is an urgent need to develop novel and chemically diverse antimalarial drugs. This study aimed at evaluating the antimalarial and antioxidant potentials of Acacia nilotica plant extracts.
The antioxidant activities of leaves, pods and bark extracts were determined by standard antioxidant assays; reducing power capacity, % lipid peroxidation inhibition and ferric reducing antioxidant power assay. The antimalarial activities of plant extracts against Plasmodium falciparum parasites were determined by the 48 h schizont maturation inhibition assay. Further confirmation of schizonticide activity of extracts was made by extending the incubation period up to 96 h after removing the plant extract residues from parasites culture. Inhibition assays were analyzed by dose-response modelling.
In all antioxidant assays, leaves of A. nilotica showed higher antioxidant activity than pods and bark. Antimalarial IC values of leaves, pods and bark extracts were 1.29, 4.16 and 4.28 μg/ml respectively, in the 48 h maturation assay. The IC values determined for leaves, pods and bark extracts were 3.72, 5.41 and 5.32 μg/ml respectively, after 96 h of incubation. All extracts inhibited the development of mature schizont, indicating schizonticide activity against P. falciparum.
A. nilotica extracts showed promising antimalarial and antioxidant effects. However, further investigation is needed to isolate and identify the active components responsible for the antimalarial and antioxidant effects.
耐药性疟疾的出现正威胁着我们在东南亚地区治疗和控制疟疾的能力。迫切需要开发新型且化学结构多样的抗疟药物。本研究旨在评估阿拉伯胶树植物提取物的抗疟和抗氧化潜力。
通过标准抗氧化试验测定叶、荚和树皮提取物的抗氧化活性;还原能力、脂质过氧化抑制率和铁还原抗氧化能力测定。通过48小时裂殖体成熟抑制试验测定植物提取物对恶性疟原虫的抗疟活性。在从寄生虫培养物中去除植物提取物残留物后,将孵育期延长至96小时,进一步确认提取物的杀裂殖体活性。通过剂量反应模型分析抑制试验。
在所有抗氧化试验中,阿拉伯胶树的叶显示出比荚和树皮更高的抗氧化活性。在48小时成熟试验中,叶、荚和树皮提取物的抗疟IC值分别为1.29、4.16和4.28μg/ml。孵育96小时后,叶、荚和树皮提取物测定的IC值分别为3.72、5.41和5.32μg/ml。所有提取物均抑制成熟裂殖体的发育,表明对恶性疟原虫具有杀裂殖体活性。
阿拉伯胶树提取物显示出有前景的抗疟和抗氧化作用。然而,需要进一步研究以分离和鉴定负责抗疟和抗氧化作用的活性成分。