Potent Protein Glycation Inhibition of Plantagoside inPlantago majorSeeds

Author:

Matsuura Nobuyasu1,Aradate Tadashi2,Kurosaka Chihiro3,Ubukata Makoto4,Kittaka Shiho1,Nakaminami Yuri1,Gamo Kanae15,Kojima Hiroyuki6,Ohara Mitsuharu6

Affiliation:

1. Department of Life Science, Faculty of Science, Okayama University of Science, 1-1 Ridai-cho, Kita-ku, Okayama 700-0005, Japan

2. University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan

3. Biotechnology Research Center, Toyama Prefectural University, 5180 Kurokawa, Kosugi-machi, Imizu-gun, Toyama 939-0398, Japan

4. Graduate School of Agriculture, Hokkaido University, Kita-9, Nishi-9, Kita-ku, Sapporo 060-8589, Japan

5. Department of Pharmaceutical Science, Graduate School of Medicine, Density and Pharmaceutical Sciences, Okayama University, 1-1-1 Tsushima-naka, Kita-ku, Okayama 700-8530, Japan

6. Ichimaru Pharcos Co., Ltd., 318-1 Asagi, Motosu-shi, Gifu 501-0475, Japan

Abstract

Plantagoside (5,7,4′,5′-tetrahydroxyflavanone-3′-O-glucoside) and its aglycone (5,7,3′,4′,5′-pentahydroxyflavanone), isolated from a 50% ethanol extract ofPlantago majorseeds (Plantaginaceae), were established to be potent inhibitors of the Maillard reaction. These compounds also inhibited the formation of advanced glycation end products in proteins in physiological conditions and inhibited protein cross-linking glycation. These results indicate thatP. majorseeds have potential therapeutic applications in the prevention of diabetic complications.

Funder

Ministry of Education, Culture, Sports, Science and Technology (MEXT)

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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