Department of Physiology, School of Oriental Medicine, Wonkwang University, Iksan, Jeonbuk, Korea.
Biol Pharm Bull. 2006 Jun;29(6):1082-6. doi: 10.1248/bpb.29.1082.
Radix Paeoniae Alba has been used as a constituent of herbal medicine prescriptions for the treatment of inflammation, cancer, and other diseases. The aim of this study was to investigate the mechanism of Radix Paeoniae Alba extract (RPAE)-induced apoptosis in HL-60 leukemic cells. We observed that RPAE induced apoptotic changes in a dose-dependent manner, which was confirmed by DNA fragmentation and poly-(ADP-ribose) polymerase (PARP) cleavage. We also found release of cytochrome c from mitochondria to the cytosol in RPAE-treated HL-60 cells. The caspases, caspase-9 and -3, but not caspase-8, were found to be activated in response to RPAE treatment, and the caspase-3 inhibitor, Ac-DEVD-CHO, and the caspase-9 inhibitor, z-LEHD-FMK, but not the caspase-8 inhibitor, z-IETD-FMK, attenuated RPAE-induced DNA fragmentation and PARP cleavage. These results suggest that RPAE-induced apoptosis is stimulated by the release of cytochrome c to the cytosol, by procaspase-9 processing, and via a caspase-3 dependent mechanism.
白芍被用作草药方剂的组成部分,用于治疗炎症、癌症等疾病。本研究旨在探讨白芍提取物(RPAE)诱导 HL-60 白血病细胞凋亡的机制。我们观察到 RPAE 诱导凋亡的变化呈剂量依赖性,这通过 DNA 片段化和多聚(ADP-核糖)聚合酶(PARP)裂解得到证实。我们还发现 RPAE 处理的 HL-60 细胞中线粒体细胞色素 c 释放到细胞质中。发现 caspase-9 和 caspase-3,但不是 caspase-8,被激活以响应 RPAE 处理,并且 caspase-3 抑制剂 Ac-DEVD-CHO 和 caspase-9 抑制剂 z-LEHD-FMK,但不是 caspase-8 抑制剂 z-IETD-FMK,减弱了 RPAE 诱导的 DNA 片段化和 PARP 裂解。这些结果表明,RPAE 诱导的细胞凋亡是通过细胞色素 c 释放到细胞质、通过前胱冬肽酶-9 加工以及通过 caspase-3 依赖的机制来刺激的。