Moringa oleifera seed methanol extract with consolidated antimicrobial, antioxidant, anti-inflammatory, and anticancer activities

被引:2
作者
El-Fakharany, Esmail M. [1 ,2 ,3 ]
Elsharkawy, Wafaa B. [4 ]
El-Maradny, Yousra A. [2 ,5 ]
El-Gendi, Hamada [6 ]
机构
[1] City Sci Res & Technol Applicat SRTA City, Genet Engn & Biotechnol Res Inst GEBRI, Prot Res Dept, Alexandria 21934, Egypt
[2] City Sci Res & Technol Applicat SRTA City, Pharmaceut & Fermentat Ind Dev Ctr, Alexandria, Egypt
[3] Pharos Univ Alexandria, Alexandria, Egypt
[4] Prince Sattam Bin Abdulaziz Univ, Coll Sci & Humanities Studies, Phys Dept, Alkharj, Saudi Arabia
[5] Arab Acad Sci Technol & Maritime Transport AASTMT, Fac Pharm, Microbiol & Immunol, El Alamein, Egypt
[6] City Sci Res & Technol Applicat SRTA City, Genet Engn & Biotechnol Res Inst, Bioproc Dev Dept, Alexandria, Egypt
关键词
anticancer; anti-inflammatory; antimicrobial; Moringa oleifera; seed extract; CANCER-CELL; DOCKING;
D O I
10.1111/1750-3841.17223
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The wide biological activity of the Moringa oleifera represents a potential opportunity for developing selective cancer treatment drugs. The bioactive phytochemicals in Moringa seed extract (MSE) indicated large numbers of phytochemicals (21 compounds) with dominant abundance for cycloisolongifolene, 8,9-dehydro-9-vinyl, and chamazulene accounting for 12.7% and 12.19% of the total detected compounds. The MSE showed a potent anticancer effect toward Caco-2, MDA, and HepG-2 cells with half-maximal inhibitory concentration (IC50) values of 9.15 +/- 1.18, 4.85 +/- 0.11, and 7.36 +/- 0.22 mu g/mL, respectively, with higher safety (>= 31-folds) toward normal human cells (IC50 of 150.7 +/- 11.11 mu g/mL). It appears that MSE stimulates selective-dose-dependent cell shrinkage, and nuclear condensation in the tumor cells, which finally induces the apoptosis pathway to increase its anticancer action. Additionally, MSE showed a potent capability to stimulate cell cycle arrest in both main checkpoint phases (G0/G1 and G2/M) of cell population growth. The apoptotic death stimulation was confirmed through upregulation of tumor protein p53 (p53) and cyclin-dependent kinase inhibitor p21 (p21) expression by more than three- to sixfold and downregulation of B-cell lymphoma 2 expression (threefold) in MSE-treated cells compared to 5-fluorouracil (5-FU)-treated tumor cells. Furthermore, the MSE revealed strong anti-inflammatory activity with significant antioxidant activity by lowering nitric oxide levels and enhancing the superoxide dismutase activity. On the other hand, the MSE revealed broad-spectrum antibacterial activity in a dose-dependent manner against Staphylococcus aureus minimum inhibitory concentration (MIC of 1.25 mg/mL), followed by Salmonella typhimurium (MIC of 1.23 mg/mL), whereas Escherichia coli was the least sensitive to MSE activity (MIC of 22.5 mg/mL) with significant antibiofilm activity against sensitive pathogens.
引用
收藏
页码:5130 / 5149
页数:20
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