Parkinsonia praecox bark as a new source of antibacterial and anticancer compounds

被引:0
|
作者
Ordaz-Hernandez, Armando [1 ]
Hernandez-Carlos, Beatriz [2 ]
Gonzalez, Hector Manuel Arreaga [2 ]
Hernandez-Ramiro, Lorena [1 ]
Ramirez, Misael Corona [1 ]
Herrera-Martinez, Mayra [1 ]
机构
[1] Univ Canada, Inst Farmacobiol, Carretera Teotitlan San Antonio Nanahuatipan Km 1-, Oaxaca 68540, Mexico
[2] Univ Tecnol Mixteca, Inst Agroind, Av Doctor Modesto Seara Vazquez 1, Oaxaca 69000, Mexico
关键词
Parkinsonia praecox; Cytotoxicity; Liver cancer; Erythrocytes; Lupenone; BIOLOGICAL-ACTIVITIES; PHYTOCHEMICAL ANALYSIS; LUPENONE; IDENTIFICATION; CONSTITUENTS; TRITERPENES;
D O I
10.1016/j.eujim.2024.102401
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Introduction: Parkinsonia praecox is used in traditional medicine to treat various diseases; however, the antibacterial and anticancer properties from its bark have not been reported. Thus, this study aimed to evaluate the antibacterial activity, cytotoxicity and chemical study of methanolic extract of Parkinsonia praecox bark (PpBM). Methods: The PpBM antibacterial activity was determined against pathogen strains using the broth microdilution method, the cytotoxic effect was assessed on cancerous (HepG2, SKOV-3 and HeLa) and non-cancerous (J774A.1 and HaCaT) cells using the crystal violet assay, the in vitro hemotoxicity was evaluated using the hemolysis assay on human erythrocytes and the identification of major compounds derived from PpBM was performed by H-1 and C-13 NMR and 2D NMR experiments. Results: PpBM (2000 mu g/mL) demonstrated antibacterial activity against Listeria monocytogenes, a potential breakthrough in the fight against this pathogen. PpBM decreased cell viability of HepG2 liver cancer cells (IC50, 104.56 mu g/mL) with a selectivity index of 1.38 regarding J774A.1 macrophages and 2.04 to HaCaT keratinocytes, suggesting a selective anticancer potential. On the other hand, PpBM did not cause hemolysis to high concentrations (1000 mu g/mL) or alterations in the morphology of human erythrocytes at doses lower than 200 mu g/mL. For the first time, lupenone, germanicone, 3-oxo-oleanane-18-en-28-ol, and combretol were identified in P. praecox. PpBM showed antibacterial, selective anticancer, and non-hemotoxic properties. These activities may be related to the major compounds, such as lupenone. Conclusion: P. praecox bark is a new option for obtaining bioactive compounds, further in vitro and in vivo studies are required to confirm their efficacy and safety.
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