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Biochemistry Research International
Volume 2016, Article ID 9347468, 11 pages
http://dx.doi.org/10.1155/2016/9347468
Research Article

Potential Properties of Plant Sprout Extracts on Amyloid β

1Nutrition Section, Ageing and Nutrition Research, Yms Laboratory, Gifu 503-1306, Japan
2Laboratory on Ageing & Health Management, Graduate School of Nursing & Health, Aichi Prefectural University, Tohgoku, Kamishidami, Moriyama, Nagoya 463-8502, Japan

Received 7 February 2016; Revised 4 April 2016; Accepted 5 May 2016

Academic Editor: Paul W. Doetsch

Copyright © 2016 Mizue Okada and Yoshinori Okada. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. C. Angeloni, L. Zambonin, and S. Hrelia, “Role of methylglyoxal in alzheimer's disease,” BioMed Research International, vol. 2014, Article ID 238485, 12 pages, 2014. View at Publisher · View at Google Scholar · View at Scopus
  2. L. Guo, R. Yang, Z. Wang, Q. Guo, and Z. Gu, “Effect of NaCl stress on health-promoting compounds and antioxidant activity in the sprouts of three broccoli cultivars,” International Journal of Food Sciences and Nutrition, vol. 65, no. 4, pp. 476–481, 2014. View at Publisher · View at Google Scholar · View at Scopus
  3. E. Chiavaro, T. Mazzeo, A. Visconti, C. Manzi, V. Fogliano, and N. Pellegrini, “Nutritional quality of sous vide cooked carrots and brussels sprouts,” Journal of Agricultural and Food Chemistry, vol. 60, no. 23, pp. 6019–6025, 2012. View at Publisher · View at Google Scholar · View at Scopus
  4. A. K. Jaiswal, G. Rajauria, N. Abu-Ghannam, and S. Gupta, “Phenolic composition, antioxidant capacity and antibacterial activity of selected Irish Brassica vegetables,” Natural Product Communications, vol. 6, no. 9, pp. 1299–1304, 2011. View at Google Scholar · View at Scopus
  5. K. Shetty and M. L. Wahlqvist, “A model for the role of the proline-linked pentose-phosphate pathway in phenolic phytochemical bio-synthesis and mechanism of action for human health and environmental applications,” Asia Pacific Journal of Clinical Nutrition, vol. 13, no. 1, pp. 1–24, 2004. View at Google Scholar · View at Scopus
  6. C. Hoelzl, J. Bichler, F. Ferk et al., “Methods for the detection of antioxidants which prevent age related diseases: a critical review with particular emphasis on human intervention studies,” Journal of Physiology and Pharmacology, vol. 56, no. 2, pp. 49–64, 2005. View at Google Scholar · View at Scopus
  7. U. Złotek, M. Świeca, and A. Jakubczyk, “Effect of abiotic elicitation on main health-promoting compounds, antioxidant activity and commercial quality of butter lettuce (Lactuca sativa L.),” Food Chemistry, vol. 148, pp. 253–260, 2014. View at Publisher · View at Google Scholar · View at Scopus
  8. C. G. Schalkwijk, C. D. A. Stehouwer, and V. W. M. van Hinsbergh, “Fructose-mediated non-enzymatic glycation: sweet coupling or bad modification,” Diabetes/Metabolism Research and Reviews, vol. 20, no. 5, pp. 369–382, 2004. View at Publisher · View at Google Scholar · View at Scopus
  9. S.-I. Yamagishi, “Potential clinical utility of advanced glycation end product cross-link breakers in age- and diabetes-associated disorders,” Rejuvenation Research, vol. 15, no. 6, pp. 564–572, 2012. View at Publisher · View at Google Scholar · View at Scopus
  10. Y. Wei, L. Chen, J. Chen, L. Ge, and R. Q. He, “Rapid glycation with D-ribose induces globular amyloid-like aggregations of BSA with high cytotoxicity to SH-SY5Y cells,” BMC Cell Biology, vol. 10, article 10, 2009. View at Publisher · View at Google Scholar · View at Scopus
  11. S. Muhammad and N. Fatima, “In silico analysis and molecular docking studies of potential angiotensin-converting enzyme inhibitor using quercetin glycosides,” Pharmacognosy Magazine, vol. 11, no. 42, pp. S123–S126, 2015. View at Publisher · View at Google Scholar
  12. T. G. Nam, S. M. Lee, J. H. Park, D. O. Kim, N. I. Baek, and S. H. Eom, “Flavonoid analysis of buckwheat sprouts,” Food Chemistry, vol. 170, pp. 97–101, 2015. View at Publisher · View at Google Scholar
  13. P. Duchnowicz, M. Bors, A. Podsedek, M. Koter-Michalak, and M. Broncel, “Effect of polyphenols extracts from Brassica vegetables on erythrocyte membranes (in vitro study),” Environmental Toxicology and Pharmacology, vol. 34, no. 3, pp. 783–790, 2012. View at Publisher · View at Google Scholar · View at Scopus
  14. V. J. Lozanovski, P. Houben, U. Hinz, T. Hackert, I. Herr, and P. Schemmer, “Pilot study evaluating broccoli sprouts in advanced pancreatic cancer (POUDER trial)—study protocol for a randomized controlled trial,” Trials, vol. 15, article 204, 2014. View at Publisher · View at Google Scholar · View at Scopus
  15. S. Awasthi and N. Saraswathi, “Sinigrin, a major glucosinolate from cruciferous vegetables restrains non-enzymatic glycation of albumin,” International Journal of Biological Macromolecules, vol. 83, pp. 410–415, 2016. View at Publisher · View at Google Scholar
  16. H. Matsuura, M. Amano, J. Kawabata, and J. Mizutani, “Isolation and measurement of quercetin glucosides in flower buds of Japanese butterbur (Petasites japonicus subsp. gigantea Kitam.),” Bioscience, Biotechnology and Biochemistry, vol. 66, no. 7, pp. 1571–1575, 2002. View at Publisher · View at Google Scholar · View at Scopus
  17. Y. Mizushina, S. Kamisuki, N. Kasai et al., “Petasiphenol: a DNA polymerase λ inhibitor,” Biochemistry, vol. 41, no. 49, pp. 14463–14471, 2002. View at Publisher · View at Google Scholar · View at Scopus
  18. Y. Hasa and H. Tazaki, “Biosynthesis of fukinolic acid isolated from Petasites japonicus,” Bioscience, Biotechnology and Biochemistry, vol. 68, no. 10, pp. 2212–2214, 2004. View at Publisher · View at Google Scholar · View at Scopus
  19. H. Shimoda, J. Tanaka, E. Yamada, T. Morikawa, N. Kasajima, and M. Yoshikawa, “Anti type I allergic property of Japanese butterbur extract and its mast cell degranulation inhibitory ingredients,” Journal of Agricultural and Food Chemistry, vol. 54, no. 8, pp. 2915–2920, 2006. View at Publisher · View at Google Scholar · View at Scopus
  20. Y. Okada and M. Okada, “Komatsuna seed extracts protection against amyloid β(1-42)-induced neuronal cell death,” Journal of Diabetes & Metabolism, vol. 5, no. 5, article 368, 2014. View at Publisher · View at Google Scholar
  21. X. Gao, M. Ohlander, N. Jeppsson, L. Björk, and V. Trajkovski, “Changes in antioxidant effects and their relationship to phytonutrients in fruits of sea buckthorn (Hippophae rhamnoides L.) during maturation,” Journal of Agricultural and Food Chemistry, vol. 48, no. 5, pp. 1485–1490, 2000. View at Publisher · View at Google Scholar · View at Scopus
  22. C. Negro, L. Tommasi, and A. Miceli, “Phenolic compounds and antioxidant activity from red grape marc extracts,” Bioresource Technology, vol. 87, no. 1, pp. 41–44, 2003. View at Publisher · View at Google Scholar · View at Scopus
  23. J. Chen, A. H. Armstrong, A. N. Koehler, and M. H. Hecht, “Small molecule microarrays enable the discovery of compounds that bind the Alzheimer's Aβ peptide and reduce its cytotoxicity,” Journal of the American Chemical Society, vol. 132, no. 47, pp. 17015–17022, 2010. View at Publisher · View at Google Scholar · View at Scopus
  24. M. Okada and Y. Okada, “Effects of methanolic extracts of edible plants on RAGE in high-glucose-induced human endothelial cells,” Bio-Medical Materials and Engineering, vol. 25, no. 3, pp. 257–266, 2015. View at Publisher · View at Google Scholar · View at Scopus
  25. Y. Okada and M. Okada, “Effects of methanolic extracts from edible plants on endogenous secretory receptor for advanced glycation end products induced by the high glucose incubation in human endothelial cells,” Journal of Pharmacy and Bioallied Sciences, vol. 7, no. 2, pp. 145–150, 2015. View at Publisher · View at Google Scholar · View at Scopus
  26. C. Lv, L. Wang, X. Liu et al., “Multi-faced neuroprotective effects of geniposide depending on the RAGE-mediated signaling in an Alzheimer mouse model,” Neuropharmacology, vol. 89, pp. 175–184, 2015. View at Publisher · View at Google Scholar · View at Scopus
  27. S.-I. Yamagishi and T. Matsui, “Role of receptor for advanced glycation end products (RAGE) in liver disease,” European Journal of Medical Research, vol. 20, article 15, 2015. View at Publisher · View at Google Scholar · View at Scopus
  28. X.-H. Li, L.-L. Du, X.-S. Cheng et al., “Glycation exacerbates the neuronal toxicity of β-amyloid,” Cell Death and Disease, vol. 4, no. 6, article e673, 2013. View at Publisher · View at Google Scholar · View at Scopus
  29. Z. Sun, J. Chen, J. Ma et al., “Cynarin-rich sunflower (Helianthus annuus) sprouts possess both antiglycative and antioxidant activities,” Journal of Agricultural and Food Chemistry, vol. 60, no. 12, pp. 3260–3265, 2012. View at Publisher · View at Google Scholar · View at Scopus
  30. Z. Bahadoran, P. Mirmiran, F. Hosseinpanah, A. Rajab, G. Asghari, and F. Azizi, “Broccoli sprouts powder could improve serum triglyceride and oxidized LDL/LDL-cholesterol ratio in type 2 diabetic patients: a randomized double-blind placebo-controlled clinical trial,” Diabetes Research and Clinical Practice, vol. 96, no. 3, pp. 348–354, 2012. View at Publisher · View at Google Scholar · View at Scopus
  31. Y. Yao, F. Chen, M. Wang, J. Wang, and G. Ren, “Antidiabetic activity of Mung bean extracts in diabetic KK-Ay mice,” Journal of Agricultural and Food Chemistry, vol. 56, no. 19, pp. 8869–8873, 2008. View at Publisher · View at Google Scholar · View at Scopus
  32. X. Mao, L. Zhang, Q. Xia et al., “Vanadium-enriched chickpea sprout ameliorated hyperglycemia and impaired memory in streptozotocin-induced diabetes rats,” BioMetals, vol. 21, no. 5, pp. 563–570, 2008. View at Publisher · View at Google Scholar · View at Scopus
  33. H. Taniguchi, K. Kobayashi-Hattori, C. Tenmyo et al., “Effect of Japanese radish (Raphanus sativus) sprout (Kaiware-daikon) on carbohydrate and lipid metabolisms in normal and streptozotocin-induced diabetic rats,” Phytotherapy Research, vol. 20, no. 4, pp. 274–278, 2006. View at Publisher · View at Google Scholar · View at Scopus
  34. J. N. Fawver, H. E. Schall, R. D. Petrofes Chapa, X. Zhu, and I. V. J. Murray, “Amyloid-β Metabolite sensing: biochemical linking of glycation modification and misfolding,” Journal of Alzheimer's Disease, vol. 30, no. 1, pp. 63–73, 2012. View at Publisher · View at Google Scholar · View at Scopus
  35. C.-H. Wu, S.-M. Huang, J.-A. Lin, and G.-C. Yen, “Inhibition of advanced glycation endproduct formation by foodstuffs,” Food and Function, vol. 2, no. 5, pp. 224–234, 2011. View at Publisher · View at Google Scholar · View at Scopus
  36. A. Bhattacherjee and A. S. Chakraborti, “Inhibitory effect of Piper betle Linn. leaf extract on protein glycation—quantification and characterization of the antiglycation components,” Indian Journal of Biochemistry and Biophysics, vol. 50, no. 6, pp. 529–536, 2013. View at Google Scholar · View at Scopus
  37. Z. Fu, D. Aucoin, M. Ahmed, M. Ziliox, W. E. Van Nostrand, and S. O. Smith, “Capping of Aβ42 oligomers by small molecule inhibitors,” Biochemistry, vol. 53, no. 50, pp. 7893–7903, 2014. View at Publisher · View at Google Scholar · View at Scopus
  38. Y. Feng, X.-P. Wang, S.-G. Yang et al., “Resveratrol inhibits beta-amyloid oligomeric cytotoxicity but does not prevent oligomer formation,” NeuroToxicology, vol. 30, no. 6, pp. 986–995, 2009. View at Publisher · View at Google Scholar · View at Scopus
  39. Z.-X. Yao, K. Drieu, and V. Papadopoulos, “The Ginkgo biloba extract EGb 761 rescues the PC12 neuronal cells from β-amyloid-induced cell death by inhibiting the formation of β-amyloid-derived diffusible neurotoxic ligands,” Brain Research, vol. 889, no. 1-2, pp. 181–190, 2001. View at Publisher · View at Google Scholar · View at Scopus