Title of article :
Screening of phytochemicals, toxicities, and activities of three Dillenia species
Author/Authors :
Siripiyasing ، Pornnarong Faculty of Science and Technology - Rajabhat Maha Sarakham University , Silawong ، Kittiya Department in biology - Faculty of Science and Technology - Bansomdejchaopraya Rajabhat University , Thooptianrat ، Tikumporn Department of Biology - Faculty of Science - Khon Kaen University , Sudmoon ، Runglawan Faculty of Law - Khon Kaen University , Babayan ، Nelly Group of Cell Technologies, Department of Genetics and Cytology - Institute of Molecular Biology, National Academy of Sciences - Yerevan State University , Khondkaryan ، Lusine Group of Cell Technologies, Department of Genetics and Cytology - Institute of Molecular Biology, National Academy of Sciences - Yerevan State University , Apresyan ، Lilit Group of Cell Technologies, Department of Genetics and Cytology - Institute of Molecular Biology, National Academy of Sciences - Yerevan State University , Tanee ، Tawatchai Faculty of Environment and Resource Studies - Mahasarakham University , Chaveerach ، Arunrat Department of Biology - Faculty of Science - Khon Kaen University
Abstract :
Introduction: Plants containing β-sitosterol and oleamide are important for various diseases. So, Dillenia indica, D. obovata, and D. pentagyna were investigated for phytochemicals, cytotoxicity and genotoxicity levels on peripheral blood mononuclear cells (PBMCs) and Hela cells. The protective effect of D. pentagyna extract on a HepG2 cell line was also investigated. Methods: Gas chromatography-mass spectrometry (GC-MS) and high-performance liquid chromatography (HPLC) were used for phytochemical analysis. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) tetrazolium reduction (MTT) and comet assays were performed for toxicity testing and protective effects against DNA oxidative damage. Results: The major components were oleamide and β-sitosterol at 38.464-58.247% and 5.585-6.887% with concentration and quantity of β-sitosterol at 0.2-0.37 mg/mL and 0.42-0.964 mg/g leaf. The D. indica, D. obovata, and D. pentagyna toxicities on PBMCs showed IC50 values at 430, 430, and 350 μg/mL respectively, with no significant DNA damage (P 0.05) compared to the negative control group. All plant extracts showed toxic activity on Hela cell with IC50 values at 0.43 μg/mL and induced significant DNA damage (P 0.05) compared to the negative control group. Conversely, the activity of the D. pentagyna extract indicated low cytotoxic activity against HepG2 (IC50 430 μg/mL), no significant (P 0.05) DNA damage induction, significantly (P 0.05) decreased DNA damage level, and tremendous antioxidant effect. Additionally, a combined mixture of all plants in an equal proportion revealed no IC50 value and insignificant DNA damage. Conclusion: All the studied species contained oleamide and β-sitosterol, with toxicity on Hela cells without toxicity on PBMC. The D. pentagyna species showed high antioxidant effects and no toxicity on HepG2.
Keywords :
Comet assay , Oleamide , Toxicity , β , Sitosterol
Journal title :
Journal of HerbMed Pharmacology
Journal title :
Journal of HerbMed Pharmacology