风铃叶乙醇提取物亚组分对人淋巴细胞和中性粒细胞的抗分枝杆菌、抗氧化和抗增殖活性的评价

M. Makgatho, W. Nxumalo, E. Ndaba, C. Masilo, F. Tsindane, M. Sedibane
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The anti-oxidant activity of the fractions was tested \nusing the radical scavenging assay, while their cytotoxicity to lymphocytes was measured using the WST-8 assay. \nReactive oxygen species production by neutrophils exposed to fractions was tested using Cell Meter™ Fluorimetric \nROS Assay kit. \nResults. The ethanolic leaf fractions exhibited overall superior anti-mycobacterial activity than the dichloromethane \ngroup and were further screened for anti-oxidant and cytotoxic activities. Ethanolic sub-fractions K2F-3.2, K2F-3.3 and \nK2F-3.4 showed significant antioxidant activities at concentration of 50 μg/ml to 200 μg/ml and higher in both the cell \nfree-based radical scavenging activity and total reactive oxygen species production assays. For lymphocytes, the test \nagents showed anti-proliferative activity at 25 μg/ml to 200 μg/ml for sub-fraction K2F-3.3B and 50 μg/ml to 200 \nμg/ml for agents K2F-3.2 and K2F-3.4. \nConclusion. 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引用次数: 3

摘要

背景。风铃草已被用于治疗各种疾病,并具有抗菌、抗炎、镇痛和止泻作用。该植物的抗结核分枝杆菌活性以及对单核细胞和中性粒细胞的细胞毒性和抗氧化活性尚未被研究。方法。采用荧光微孔板法筛选堇叶乙醇和二氯甲烷提取物(0.2 ~ 125μg/ml)的抗分枝杆菌活性。用自由基清除法检测其抗氧化活性,用WST-8法检测其对淋巴细胞的细胞毒性。使用Cell Meter™荧光ROS检测试剂盒检测暴露于馏分中的中性粒细胞产生的活性氧。结果。乙醇叶组分总体上表现出比二氯甲烷组更强的抗分枝杆菌活性,并进一步进行了抗氧化和细胞毒活性筛选。乙醇亚组分K2F-3.2、K2F-3.3和K2F-3.4在浓度为50 ~ 200 μg/ml及更高浓度时,细胞自由基清除活性和总活性氧生成均表现出显著的抗氧化活性。对淋巴细胞,K2F-3.3B亚组分具有25 ~ 200 μg/ml的抗增殖活性,K2F-3.2和K2F-3.4亚组分具有50 ~ 200 μg/ml的抗增殖活性。结论。本研究首次在给定的实验条件下记录了芦花叶提取物亚组分的体外抗分枝杆菌、抗氧化和细胞毒活性,并进行了进一步的研究以确定其生物活性成分。
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EVALUATION OF THE ANTI-MYCOBACTERIAL, ANTI-OXIDATIVE AND ANTI-PROLIFERATIVE ACTIVITIES OF RUBIA CORDIFOLIA ETHANOLIC LEAF EXTRACT SUB-FRACTIONS IN HUMAN LYMPHOCYTES AND NEUTROPHILS
Background. Rubia cordifolia has been used to treat various diseases and exhibits antimicrobial, anti-inflammatory, analgesic and antidiarrheal activities. The plant has not been investigated for its anti-mycobacterial activity against virulent tuberculosis strains as well as cytotoxic and anti-oxidant activities in mononuclear cells and neutrophils. Methods. Ethanolic and dichloromethane leaf extract fractions of Rubia cordifolia (0.2- 125μg/ml) were screened for anti-mycobacterial activity using a fluorescent microplate assay. The anti-oxidant activity of the fractions was tested using the radical scavenging assay, while their cytotoxicity to lymphocytes was measured using the WST-8 assay. Reactive oxygen species production by neutrophils exposed to fractions was tested using Cell Meter™ Fluorimetric ROS Assay kit. Results. The ethanolic leaf fractions exhibited overall superior anti-mycobacterial activity than the dichloromethane group and were further screened for anti-oxidant and cytotoxic activities. Ethanolic sub-fractions K2F-3.2, K2F-3.3 and K2F-3.4 showed significant antioxidant activities at concentration of 50 μg/ml to 200 μg/ml and higher in both the cell free-based radical scavenging activity and total reactive oxygen species production assays. For lymphocytes, the test agents showed anti-proliferative activity at 25 μg/ml to 200 μg/ml for sub-fraction K2F-3.3B and 50 μg/ml to 200 μg/ml for agents K2F-3.2 and K2F-3.4. Conclusion. The current study is the first to record the in vitro anti-mycobacterial, anti-oxidant and cytotoxic activities of Rubia cordifolia plant leaf extract sub-fractions using the given experimental setups and further research activities to identify the bioactive components are to be pursued.
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期刊介绍: The “African Journal of Traditional, Complementary and Alternative Medicines (AJTCAM)” is a peer-reviewed, multidisciplinary, international, scientific Open Access Journal that provides publication of articles on phytomedicines, ethnomedicines and veterinary ethnomedicines. The journal is published by a Non-Governmental Organization (NGO) known as “African Traditional Herbal Medicine Supporters Initiative (ATHMSI)”. The Journal welcomes submission of manuscripts that meet the general criteria of significance and scientific excellence. Papers will be published approximately two-to-three months after acceptance
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