Min-Gyung Son, Pel Pisey, An Chae-Yeong, Park Chan-Woong, Lee Sae Hyun, Yang Tae-Jin, Chin Young-Won
Natural Products Research Institute and Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, 08826, Republic of Korea.
Department of Agriculture, Forestry and Bioresources, Plant Genomics & Breeding Institute, Research Institute of Agriculture and Life Sciences, College of Agriculture & Life Sciences, Seoul National University, Seoul, 08826, Republic of Korea.
Phytochemistry. 2024 Oct;226:114205. doi: 10.1016/j.phytochem.2024.114205. Epub 2024 Jul 4.
From the Cynanchum wilfordii roots, 32 compounds, including 5 previously undescribed (1, 4-6, 12) and 27 known (2, 3, 7-11, 13-32) compounds, were isolated, and their structures were elucidated using NMR spectroscopic data and MS data aided by ECD calculations or the modified Mosher's reaction. All isolates were tested for their inhibitory effects on proprotein convertase subtilisin/kexin type 9 (PCSK9) secretion. Among the isolates, compound 4, a methyl cholesterol analog, exhibited the most potent effect in reducing PCSK9 secretion, along with PCSK9 downregulation at the mRNA and protein levels via FOXO1/3 upregulation. Moreover, compound 4 attenuated statin-induced PCSK9 expression and enhanced the uptake of DiI-LDL low-density lipoprotein. Thus, compound 4 is suggested to be a potential candidate for controlling cholesterol levels.
从白首乌根中分离出32种化合物,其中包括5种此前未描述的化合物(1、4 - 6、12)和27种已知化合物(2、3、7 - 11、13 - 32),并利用核磁共振光谱数据和质谱数据,借助电子圆二色光谱计算或改良的莫舍尔反应阐明了它们的结构。对所有分离出的化合物进行了前蛋白转化酶枯草杆菌蛋白酶/kexin 9型(PCSK9)分泌抑制作用的测试。在这些分离出的化合物中,化合物4(一种甲基胆固醇类似物)在降低PCSK9分泌方面表现出最显著的效果,同时通过上调FOXO1/3在mRNA和蛋白质水平下调PCSK9。此外,化合物4减弱了他汀类药物诱导的PCSK9表达,并增强了DiI - 低密度脂蛋白(LDL)的摄取。因此,化合物4被认为是控制胆固醇水平的潜在候选物。