3-(4-Hydroxy-3-methoxyphenyl) propionic acid contributes to improved hepatic lipid metabolism via GPR41

被引:8
|
作者
Ohue-Kitano, Ryuji [1 ,2 ,3 ]
Masujima, Yuki [1 ]
Nishikawa, Shota [2 ]
Iwasa, Masayo [1 ]
Nishitani, Yosuke [4 ]
Kawakami, Hideaki [4 ]
Kuwahara, Hiroshige [4 ]
Kimura, Ikuo [1 ,2 ,5 ]
机构
[1] Kyoto Univ, Grad Sch Biostudies, Lab Mol Neurobiol, Yoshidakonoe Cho,Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Grad Sch Pharmaceut Sci, Lab Mol Endocrinol, Kyoto 6068501, Japan
[3] Kyoto Univ, Ctr Living Syst Informat Sci CeLiSIS, Kyoto 6068501, Japan
[4] Maruzen Pharmaceut Co Ltd, Res Ctr, Fukuyama, Hiroshima 7293102, Japan
[5] Tokyo Univ Agr & Technol, Grad Sch Agr, Dept Appl Biol Sci, Fuchu, Tokyo 1838509, Japan
关键词
COFFEE;
D O I
10.1038/s41598-023-48525-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
3-(4-hydroxy-3-methoxyphenyl) propionic acid (HMPA) is a metabolite produced by the gut microbiota through the conversion of 4-hydroxy-3-methoxycinnamic acid (HMCA), which is a widely distributed hydroxycinnamic acid-derived metabolite found abundantly in plants. Several beneficial effects of HMPA have been suggested, such as antidiabetic properties, anticancer activities, and cognitive function improvement, in animal models and human studies. However, the intricate molecular mechanisms underlying the bioaccessibility and bioavailability profile following HMPA intake and the substantial modulation of metabolic homeostasis by HMPA require further elucidation. In this study, we effectively identified and characterized HMPA-specific GPR41 receptor, with greater affinity than HMCA. The activation of this receptor plays a crucial role in the anti-obesity effects and improvement of hepatic steatosis by stimulating the lipid catabolism pathway. For the improvement of metabolic disorders, our results provide insights into the development of functional foods, including HMPA, and preventive pharmaceuticals targeting GPR41.
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页数:11
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