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Effect of supplemented soybean (Glycine max L) diet and extracts on aluminum sulfate-induced genotoxicity
Authors:Hanan A Al-Ashaal  Maha A Fahmy  Farouk R Melek  Nagwa H Aly  Zenab M Hasan
Institution:1. Pharmaceutical and Drug Industries Division , National Research Centre , Dokki , Giza , Egypt hanan_alashaal@yahoo.com;3. Cytogenetic Department , National Research Centre , Dokki , Giza , Egypt;4. Pharmaceutical and Drug Industries Division , National Research Centre , Dokki , Giza , Egypt;5. Zoology Department, Faculty of Science , Ain Shams University , Cairo , Egypt
Abstract:Aim of this study is to evaluate the protective role of Glycine max L. (soybean) against aluminum sulfate-induced genotoxicity. A diet containing 30% soybean and extracts obtained with various organic solvents were administered orally to male white Swiss mice prior to intraperitoneal injection of Al2(SO4)3. Light microscopy was used for the examination of genotoxicity involving somatic cells, germ cells, and sperms. The main secondary metabolites contained in each extract were isolated and identified by chromatographic and spectral analyses. Administration of soy diet and extracts to the examined mice induced significant anti-mutagenic activity against bone marrow aberrations and spermatocyte and sperm abnormalities. At the end of this study, maximum protection was achieved using the methanolic extract (83% and 79%) followed by those obtained with chloroform (71% and 49%) and n-hexane (51% and 39%) for bone marrow aberrations and spermatocyte abnormalities, respectively. The observed activity of soybean extracts might be related to the main constituents isolated and identified. These main constituents were the isoflavone glycosides genistin and daidzin in addition to saponins (methanol extract), lignan matairesinol (chloroform extract), and β-sitosterol, unsaturated fatty acids as well as phospholipids (n-hexane extract). The results illustrated that soy extracts can be considered as alternative anti-mutagenic nutraceuticals and promising source for developing anti-mutagenic drugs.
Keywords:Glycine max  active constituents  bioflavonoids  anti-mutagenicity  aluminium sulfate
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