Tun Tint Ni Ni, Yoshino Susumu, Kayaki Hiroyuki, Kuwahara Hiroshige, Matsui Toshiro
Department of Bioscience and Biotechnology, Faculty of Agriculture, Graduate School of Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
Research Center, Maruzen Pharmaceuticals Co., Ltd., Fukuyama 729-3102, Japan.
ACS Omega. 2025 Jan 16;10(3):2887-2896. doi: 10.1021/acsomega.4c09008. eCollection 2025 Jan 28.
We aimed to clarify whether metabolic conjugates of sulfated and glucuronidated forms have the physiological potential to produce the vasorelaxant nitric oxide (NO) in human umbilical vein endothelial cells (HUVECs), using 3-(4-hydroxy-3-methoxyphenyl) propionic acid (HMPA), a metabolite of dietary flavonoids in the gut. Treatment of HUVECs with sulfated and glucuronidated HMPAs significantly increased NO production and eNOS phosphorylation. A transporter-inhibitor-aided cellular uptake experiment of HMPAs revealed that both conjugates were incorporated into cells via MCT, OATP1A2, and GLUT transporters, whereas intact HMPA was transported via the MCT and OATP1A2 routes. A Fluo-4-probe Ca assay demonstrated that the incorporated HMPAs significantly increased intracellular Ca concentration by stimulating the IPR of the endoplasmic reticulum in the CaMKII/eNOS signaling cascade. In conclusion, to our knowledge, this study provides the first evidence that sulfated and glucuronidated forms of HMPAs may stimulate NO production in HUVECs.
我们旨在利用肠道中膳食类黄酮的代谢产物3-(4-羟基-3-甲氧基苯基)丙酸(HMPA),阐明硫酸化和葡萄糖醛酸化形式的代谢共轭物是否具有在人脐静脉内皮细胞(HUVECs)中产生血管舒张性一氧化氮(NO)的生理潜力。用硫酸化和葡萄糖醛酸化的HMPAs处理HUVECs可显著增加NO的产生和eNOS磷酸化。HMPAs的转运体抑制剂辅助细胞摄取实验表明,两种共轭物均通过MCT、OATP1A2和GLUT转运体进入细胞,而完整的HMPA则通过MCT和OATP1A2途径转运。Fluo-4探针钙测定表明,摄入的HMPAs通过刺激CaMKII/eNOS信号级联反应中内质网的IPR显著增加细胞内钙浓度。总之,据我们所知,本研究首次提供了证据,表明硫酸化和葡萄糖醛酸化形式的HMPAs可能刺激HUVECs中NO的产生。