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Myricetin and quercetin are naturally occurring co-substrates of cyclooxygenases in vivo
Authors:Hyoung-Woo Bai  Bao Ting Zhu
Institution:1. College of Biological and Environmental Engineering, Zhejiang University of Technology, Hangzhou, 310032, China;2. Vascular Biology and Therapeutics Program, School of Medicine, Yale University, New Haven, CT, 06511, USA;1. Department of Toxicology, College of Pharmacy, Chungnam National University, Daejeon, Republic of Korea;2. Department of Pharmaceutical Engineering, International University of Korea, Jinju, Republic of Korea;3. Asan Institute for Life Sciences, Asan Medical Center, Seoul, Republic of Korea;4. Jeollanamdo Institute of Natural Resources Research, Jeollanamdo, Republic of Korea;5. Department of Food Science, International University of Korea, Jinju, Republic of Korea;6. Jangsaeng Doraji Co., Ltd., Jinju, Republic of Korea;1. Toxicology Program, Integrated Laboratory Systems, Inc., PO Box 13501, Research Triangle Park, NC 27709, USA;2. Maronpot Consulting LLC, 1612 Medfield Road, Raleigh, NC 27607, USA;3. Global Scientific and Regulatory Affairs, San-Ei Gen F.F.I., Inc., 1-1-11 Sanwa-cho, Toyonaka, Osaka 561-8588, Japan
Abstract:Bioflavonoids are ubiquitously present in the plant kingdom, and some of them are presently being sold as healthy dietary supplements around the world. Recently, it was shown that some of the dietary polyphenols were strong stimulators of the catalytic activity of cyclooxygenase I and II, resulting in increased formation of certain prostaglandin (PG) products in vitro and also in intact cells in culture. In the present study, we investigated the effect of two representative dietary compounds, quercetin and myricetin, on plasma and tissue levels of several PG products in normal Sprague-Dawley rats. We found that these two dietary bioflavonoids could strongly stimulate the formation of PG products in vivo in a time-dependent manner, and the stimulatory effect of these two bioflavonoids was dose-dependent with a unique biphasic pattern. At lower doses (<0.3 mg/kg b.w.), they strongly stimulated the formation of PGE2, but at higher doses (>0.3 mg/kg b.w.), there was a dose-dependent reduction of the stimulatory effect. These results provide support for the hypothesis that some of the bioflavonoids are naturally occurring physiological co-substrates for the cyclooxygenases in vivo.
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