References
- Aherne SA, O’Brien NM. 2002. Dietary flavonols: chemistry, food content, and metabolism. Nutrition. 18:75–81.
- Blaut M, Schoefer L, Braune A. 2003. Transformation of flavonoids by intestinal microorganisms. Int J Vitam Nutr Res. 73:79–87.
- Bravo L. 1998. Polyphenols: chemistry, dietary sources, metabolism, and nutritional significance. Nutr Rev. 56:317–333.
- Cook MA, Karmazyn M. 1996. Cardioprotective actions of adenosine and adenosine analogs. EXS. 76:325–344.
- Del Rio D, Borges G, Crozier A. 2010. Berry flavonoids and phenolics: bioavailability and evidence of protective effects. Br J Nutr. 104:S67–S90.
- Du L-Y, Zhao M, Xu J, Qian D-W, Jiang S, Shang E-X, Guo J-M, Liu P, Su S-L, Duan J-A, et al. 2014. Identification of the metabolites of myricitrin produced by human intestinal bacteria in vitro using ultra-performance liquid chromatography/quadrupole time-of-flight mass spectrometry. Expert Opin Drug Metab Toxicol. 10:921–931.
- Griffiths LA, Smith GE. 1972. Metabolism of myricetin and related compounds in the rat. Metabolite formation in vivo and by the intestinal microflora in vitro. Biochem J. 130:141–151.
- Hardigree AA, Epler JL. 1978. Comparative mutagenesis of plant flavonoids in microbial systems. Mutat Res. 58:231–239.
- Hatcher JF, Bryan GT. 1985. Factors affecting the mutagenic activity of quercetin for Salmonella typhimurium TA98: metal ions, antioxidants and pH. Mutat Res. 148:13–23.
- Hobbs CA, Swartz C, Maronpot RR, Davis J, Recio L, Hayashi S. 2015. Genotoxicity evaluation of the flavonoid myricitrin and it aglycone myricetin. Food Chem Toxicol. 83:283–292.
- ILAR. 2011. Guide for the care and use of laboratory animals. 8th ed. Washington (DC): The National Academies Press; 220 p.
- JECFA. 2014. Food additives and flavorings. 79th Meeting, Geneva. Available from: http://www.fao.org/food/food-safety-quality/scientific-advice/calls-data-experts/en/
- MacGregor JT, Jurd L. 1978. Mutagenicity of plant flavonoids: structural requirements for mutagenic activity in Salmonella typhimurium. Mutat Res. 54:297–309.
- Matsukawa N, Matsumoto M, Hara H. 2012. 35. Nondigestible saccharide enhances transcellular transport of myricetin glycosides in the small intestine of rats. A newly defined mechanism of flavonoid absorption. In: Cho S, Almeida N, editors. Dietary fiber and health. New York: CRC Press; p. 487–496.
- Matsumoto M, Matsukawa N, Chiji H, Hara H. 2007. Difructose Anhydride III promotes absorption of the soluble flavonoid αG-rutin in rats. J Agric Food Chem. 55:4202–4208.
- OECD. 2010. OECD guideline for the testing of chemicals. Toxicokinetics. [Internet]. OECD 417. [cited 2010 Jul 22]. Available from: www.oecd-library.org
- Ong KC, Khoo H-E. 1997. Biological effects of myricetin. Gen Pharmacol. 29:121–126.
- Sahu SC, Gray GC. 1993. Interactions of flavonoids, trace metals, and oxygen: nuclear DNA damage and lipid peroxidation induced by myricetin. Cancer Lett. 70:73–79.
- Schwanke RC, Marcon R, Meotti FC, Bento AF, Dutra RC, Pizzollatti MG, Calixto JB. 2013. Oral administration of the flavonoid myricitrin prevents dextran sulfate sodium-induced experimental colitis in mice through modulation of PI3K/Akt signaling pathway. Mol Nutr Food Res. 57:1938–1949.
- Smith GE, Griffiths LA. 1970. Metabolism of myricitrin and 3,4,5-trihydroxyphenylacetic acid. Biochem J. 118:53P–54P.
- Smith R, Waddell W, Cohen S, Vj F, Marnett L, Portoghese P, Rietjens I, Adams T, Lucal Gavin C, McGowen M, et al. 2009. GRAS Flavoring Substances 24. Food Technology. 06:46–105.
- Wolffram S, Block M, Ader P. 2002. Quercetin-3-glucoside is transported by the glucose carrier SGLT1 across the brush border membrane of rat small intestine. J Nutr. 132:630–635.
- Yokomizo A, Moriwaki M. 2005. Transepithelial permeability of myricitrin and its degradation by simulated digestion in human intestinal Caco-2 cell monolayer. Biosci Biotechnol Biochem. 69:1774–1776.
- Yoshino H, Kawabe M, Tamano S, Hagiwara A, Washino T, Nakamura M, Imaida K. 2001. 1-year oral toxicity study of Chinese bayberry extract in F344/DuCrj rats. Jpn J Food Chem. 8:94–99.