Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41, Shinagawa-ku, Tokyo, 142-8501, Japan.
J Nat Med. 2024 Jan;78(1):216-225. doi: 10.1007/s11418-023-01740-8. Epub 2023 Sep 5.
A dimeric indole alkaloid, isovincathicine consisting of an aspidosperma type and modified iboga with C-7-C-20 connection type skeletons was first isolated from Catharanthus roseus, and the structure including stereochemistry was elucidated on the basis of spectroscopic data as well as DP4 statistical analysis. Isovincathicine inhibited cell proliferation in A549 cells. We investigated the detailed mode of action of isovincathicine-induced inhibitory effects on cell proliferation in A549 cells. Flow cytometric analysis showed that isovincathicine-treated cells accumulated in the G phase after 24 h, and the percentage of cells showing cell death increased after 48 h. Western blotting also showed increased expression of BimEL, an apoptosis-related protein, and decreased expression of Mcl-1 and Bcl-xL. Isovincathicine was suggested to induce apoptosis in A549 cells by a mechanism is similar to that of vinblastine.
一种二聚吲哚生物碱,异长春新碱,由一个阿皮多斯帕玛型和修饰的伊博加组成,具有 C-7-C-20 连接骨架,最初从长春花中分离出来,其结构包括立体化学,是基于光谱数据以及 DP4 统计分析来阐明的。异长春新碱抑制 A549 细胞的增殖。我们研究了异长春新碱诱导的对 A549 细胞增殖抑制作用的详细作用模式。流式细胞术分析显示,异长春新碱处理的细胞在 24 小时后积累在 G 期,并且在 48 小时后显示细胞死亡的细胞百分比增加。Western blot 也显示凋亡相关蛋白 BimEL 的表达增加,而 Mcl-1 和 Bcl-xL 的表达减少。异长春新碱通过类似于长春碱的机制诱导 A549 细胞凋亡。