Key Laboratory of TCM-Information Engineer of State Administration of TCM, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 100029, China.
Int J Mol Sci. 2024 Aug 5;25(15):8548. doi: 10.3390/ijms25158548.
Plantaginis semen is the dried ripe seed of L. or Willd., which has a long history in alleviating hyperuricemia (HUA) and chronic kidney diseases. While the major chemical ingredients and mechanism remained to be illustrated. Therefore, this work aimed to elucidate the chemicals and working mechanisms of PS for HUA. UPLC-QE-Orbitrap-MS was applied to identify the main components of PS in vitro and in vivo. RNA sequencing (RNA-seq) was conducted to explore the gene expression profile, and the genes involved were further confirmed by real-time quantitative PCR (RT-qPCR). A total of 39 components were identified from PS, and 13 of them were detected in the rat serum after treating the rat with PS. The kidney tissue injury and serum uric acid (UA), xanthine oxidase (XOD), and cytokine levels were reversed by PS. Meanwhile, renal urate anion transporter 1 () and glucose transporter 9 () levels were reversed with PS treatment. RNA-seq analysis showed that the PPAR signaling pathway; glycine, serine, and threonine metabolism signaling pathway; and fatty acid metabolism signaling pathway were significantly modified by PS treatment. Further, the gene expression of , , , and were significantly elevated, and was downregulated, consistent with RNA-seq results. The PPAR signaling pathway involved , , , , , and were elevated by PS treatment. URAT1 and PPARα proteins levels were confirmed by Western blotting. In conclusion, this study elucidates the chemical profile and working mechanisms of PS for prevention and therapy of HUA and provides a promising traditional Chinese medicine agency for HUA prophylaxis.
车前子是车前科或车前属植物的干燥成熟种子,具有缓解高尿酸血症(HUA)和慢性肾脏病的悠久历史。然而,其主要化学成分和作用机制仍有待阐明。因此,本研究旨在阐明车前子治疗 HUA 的化学成分和作用机制。采用 UPLC-QE-Orbitrap-MS 鉴定车前子的主要成分。进行 RNA 测序(RNA-seq)以探讨基因表达谱,并通过实时定量 PCR(RT-qPCR)进一步验证涉及的基因。从车前子中鉴定出 39 种成分,其中 13 种在大鼠用车前子处理后在血清中检测到。车前子可逆转肾脏组织损伤和血清尿酸(UA)、黄嘌呤氧化酶(XOD)和细胞因子水平。同时,车前子治疗可逆转肾脏尿酸盐阴离子转运蛋白 1(URAT1)和葡萄糖转运蛋白 9(GLUT9)水平。RNA-seq 分析表明,车前子处理显著调节过氧化物酶体增殖物激活受体(PPAR)信号通路、甘氨酸、丝氨酸和苏氨酸代谢信号通路以及脂肪酸代谢信号通路。此外, 、 、 、 、 基因的表达显著升高, 基因下调,与 RNA-seq 结果一致。PPAR 信号通路涉及 、 、 、 、 和 ,车前子处理可上调这些基因。Western blot 进一步验证了 URAT1 和 PPARα 蛋白水平。综上所述,本研究阐明了车前子预防和治疗 HUA 的化学成分和作用机制,为 HUA 预防提供了一种有前途的中药制剂。