The Preparation of Preserved Shallot Powders and a Pilot Study of the Antioxidative Effect of Their Aqueous Extracts on the Formation of Hydroxyl Radical Species

Abstract

In order to preserve the nutrients in shallots, after harvest, various protocols, including incubation, drying or lyophilization of the shallot are developed in this study. Using aqueous extracts of ground shallot powders, this study examines the antioxidative properties of shallots on the formation of hydroxyl radical species (.OH) generated via a Fenton-type reaction. A ribose degradation assay shows that all aqueous extracts of shallot prepared in this study exhibit enhanced levels of .OH, suggesting that processed shallot, like strong reductants such as ascorbate, has a strong reducing power, which converts FeIII to FeII in a Fenton’s reaction and increases the levels of .OH. A DNA integrity assay shows that fragmentation of super-coiled plasmid DNA, pGEM-7Zf(-), by .OH is diminished in the presence of all shallot aqueous extracts, albeit to various extents. Finally, electron paramagnetic resonance (EPR) experiments show that lyophilized shallot completely scavenges .OH, as evidenced by the disappearance of the EPR-active reaction product generated between spin trap, 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), and ?OH. The results of this study show the potential of a daily intake of preserved shallot to boost antioxidative protection against the toxicity of ?OH or any other damaging radicals.

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J. Liang, A. Hsu, X. Lan, K. Chen, P. Chen, W. Chou, K. Liou, D. Peng and J. Yuann, "The Preparation of Preserved Shallot Powders and a Pilot Study of the Antioxidative Effect of Their Aqueous Extracts on the Formation of Hydroxyl Radical Species," Open Journal of Applied Sciences, Vol. 2 No. 4, 2012, pp. 209-215. doi: 10.4236/ojapps.2012.24031.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] S. V. Jovanovic, S. Steenken, M. Tosic and M. G. Simic, “Flavonoids as Antioxidants,” Journal of the American Chemical Society, Vol. 116s, No. 11, 1994, pp. 48464851. doi:10.1021/ja00090a032
[2] C. A. Rice-Evans, N. J. Miller and G. Paganga, “Structure-Antioxidant Activity Relationships of Flavonoids and Phenolic Acids,” Free Radical Biology and Medicine, Vol. 20s, No. 7, 1996, pp. 933-956. doi:10.1016/0891-5849(95)02227-9
[3] A. T. Diplock, J. L. Charleux, G. Crozier-Willi, F. J. Kok, C. Rice-Evans, M. Roberfroid, W. Stahl and J. VinaRibes, “Functional Food Science and Defence against Reactive Oxidative Species,” British Journal of Nutrition, Vol. 80, No. 1, 1998, pp. S77-S112.
[4] F. Liu and T. B. Ng, “Antioxidative and free radical scavenging activities of selected medicinal herbs,” Life Sciences, Vol. 66s, No. 8, 2000, pp. 725-735. doi:10.1016/S0024-3205(99)00643-8
[5] C. Huang, X. Zhang, Z. Qiao, L. Guan, S. Peng, J. Liu, R. Xie and L. Zheng, “A Case-Control Study of Dietary Factors in Patients with Lung Cancer,” Biomedical and Environmental Sciences, Vol. 5s, No. 3, 1992, pp. 257-265.
[6] E. Fattorusso, M. Iorizzi, V. Lanzotti and O. Taglialatela-Scafati, “Chemical Composition of Shallot (Allium ascalonicum Hort.),” Journal of Agricultural and Food Chemistry, Vol. 50s, No. 20, 2002, pp. 5686-5690. doi:10.1021/jf020396t
[7] J. Kiviranta, K. Huovinen and R. Hiltunen, “Variation of Phenolic Substances in Onion,” Acta pharmaceutica Fennica, Vol. 97s, No. 2, 1988, pp. 67-72.
[8] L. Terrance, G. Charles, F. Larry, K. H. William, C. Jose and N. Vicente, “Molecular Characterization of Quercetin and Quercetin Glycosides in Allium Vegetables. Their Effects on Malignant Cell Transformation,” ACS Symposium Series, Vol. 50s, 1992, pp. 220-238.
[9] A. S. Salim, “Oxygen-Derived Free-Radical Scavengers Prolong Survival in Gastric Cancer,” Chemotherapy, Vol. 38s, No. 2, 1992, pp. 135-144. doi:10.1159/000238953
[10] M. Tatsuta, H. Iishi, M. Baba, T. Mikuni, H. Narahara, N. Uedo and H. Yano, “Suppression by Iron Chelator Phenanthroline of Sodium Chloride-Enhanced Gastric Carcinogenesis Induced by N-methyl-N’-nitro-N-nitrosoguanidine in Wistar Rats,” Cancer Letters, Vol. 191s, No. 1, 2003, pp. 9-16. doi:10.1016/S0304-3835(01)00797-2
[11] Y. Zhou, W. Zhuang, W. Hu, G. J. Liu, T. X. Wu and X. T. Wu, “Consumption of Large Amounts of Allium Vegetables Reduces Risk for Gastric Cancer in a MetaAnalysis,” Gastroenterology, Vol. 141s, No. 1, 2011, pp. 80-89. doi:10.1053/j.gastro.2011.03.057
[12] J. Y. Kim and O. Kwon, “Garlic Intake and Cancer Risk: An Analysis Using the Food and Drug Administration’s Evidence-Based Review System for the Scientific Evaluation of Health Claims,” The American Journal of Clinical Nutrition, Vol. 89s, No. 1, 2009, pp. 257-264.
[13] N. Leelarungrayub, V. Rattanapanone, N. Chanarat and J. M. Gebicki, “Quantitative Evaluation of the Antioxidant Properties of Garlic and Shallot Preparations,” Nutrition, Vol. 22s, No. 3, 2006, pp. 266-274. doi:10.1016/j.nut.2005.05.010
[14] A. Toure, X. Xu, T. Michel and M. Bangoura, “In Vitro Antioxidant and Radical Scavenging of Guinean Kinkeliba Leaf (Combretum micranthum G. Don) Extracts,” Natural Product Research, Vol. 25s, No. 11, 2011, pp. 1025-1036. doi:10.1080/14786419.2010.482048
[15] G. K. Lopes, H. M. Schulman and M. Hermes-Lima, “Polyphenol Tannic Acid Inhibits Hydroxyl Radical Formation from Fenton Reaction by Complexing Ferrous ions,” Biochimica et Biophysica Acta, Vol. 1472s, No. 1-2, 1999, pp. 142-152. doi:10.1016/S0304-4165(99)00117-8
[16] M. J. Burkitt and B. C. Gilbert, “Model Studies of the Iron-Catalysed Haber-Weiss Cycle and the AscorbateDriven Fenton Reaction,” Free Radical Research Communications, Vol. 10s, No. 4-5, 1990, pp. 265-280. doi:10.3109/10715769009149895
[17] W. K. Pogozelski and T. D. Tullius, “Oxidative Strand Scission of Nucleic Acids: Routes Initiated by Hydrogen Abstraction from the Sugar Moiety,” Chemical Reviews, Vol. 98s, No. 3, 1998, pp. 1089-1107. doi:10.1021/cr960437i
[18] R. A. Floyd, “Hydroxyl Free-Radical Spin-Adduct in Rat Brain Synaptosomes. Observations on the Reduction of the Nitroxide,” Biochimica et Biophysica Acta, Vol. 756s, No. 2, 1983, pp. 204-216. doi:10.1016/0304-4165(83)90093-4
[19] B. Torok, J. Belagyi, B. Rietz and R. Jacob, “Effectiveness of Garlic on the Radical Activity in Radical Generating Systems,” Arzneimittelforschung, Vol. 44s, No. 5, 1994, pp. 608-611.
[20] B. Yavuz, E. Bilensoy, I. Vural and M. Sumnu, “Alternative Oral Exemestane Formulation: Improved Dissolution and Permeation,” International Journal of Pharmaceutics, Vol. 398s, No. 1-2, 2010, pp. 137-145. doi:10.1016/j.ijpharm.2010.07.046
[21] B. Balasubramanian, W. K. Pogozelski and T. D. Tullius, “DNA Strand Breaking by the Hydroxyl Radical Is Governed by the Accessible Surface Areas of the Hydrogen Atoms of the DNA Backbone,” Proceedings of the National Academy of Sciences of the United States of America, Vol. 95s, No. 17, 1998, pp. 9738-9743. doi:10.1073/pnas.95.17.9738
[22] M. A. Price and T. D. Tullius, “How the Structure of an Adenine Tract Depends on Sequence Context: A New Model for the Structure of TnAn DNA Sequences,” Biochemistry, Vol. 32s, No. 1, 1993, pp. 127-136. doi:10.1021/bi00052a018
[23] E. O. Hole, W. H. Nelson, E. Sagstuen and D. M. Close, “Free Radical Formation in X-Irradiated Anhydrous Crystals of Inosine Studied by EPR and ENDOR Spectroscopy,” Radiation Research, Vol. 130s, No. 2, 1992, pp. 148-159. doi:10.2307/3578271
[24] D. M. Close, “Where Are the Sugar Radicals in Irradiated DNA?” Radiation Research, Vol. 147s, No. 6, 1997, pp. 663-673. doi:10.2307/3579478
[25] S. Tuntipopipat, C. Zeder, P. Siriprapa and S. Charoenkiatkul, “Inhibitory Effects of Spices and Herbs on Iron Availability,” International Journal of Food Sciences and Nutrition, Vol. 60 s, No. S1, 2009, pp. 43-55.
[26] A. J. Carmichael, K. Makino and P. Riesz, “Quantitative Aspects of ESR and Spin Trapping of Hydroxyl Radicals and Hydrogen Atoms in Gamma-Irradiated Aqueous Solutions,” Radiation Research, Vol. 100s, No. 2, 1984, pp. 222-234. doi:10.2307/3576343

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