Shashi Bhushan, Jaswant Singh, Madhusudana Rao J, Kumar Saxena A, Nabi Qazi G
Division of Pharmacology, Regional Research Laboratory (Council of Scientific and Industrial Research), Jammu Tawi, India.
Nitric Oxide. 2006 Feb;14(1):72-88. doi: 10.1016/j.niox.2005.09.009. Epub 2005 Nov 8.
AP9-cd, a standardized lignan composition from Cedrus deodara consisting of (-)-wikstromal, (-)-matairesinol, and dibenzyl butyrolactol, showed cytotoxicity in several human cancer cell lines reported earlier. An attempt was made in this study to investigate the mechanism of cell death in human leukemia Molt-4 and HL-60 cells. It inhibited Molt-4 cell proliferation with 48-h IC(50) of approximately 15 microg/ml, increased sub-G0 cell fraction with no mitotic block, produced apoptotic bodies and induced DNA ladder formation. Flow cytometric analysis of annexinV-FITC/PI-stained cells showed time-related increase in apoptosis and post-apoptotic necrosis. All these biological end-points indicated cell death by apoptosis. Further, initial events involved massive nitric oxide (NO) formation within 4 h with subsequent late appearance of peroxides in cells; measured by flow cytometry using specific fluorescent probes. Persistently high levels of NO and peroxide appeared to decrease mitochondrial membrane potential (Psi(mt)) which was recovered by cyclosporin A in Molt-4 cells. AP9-cd caused 2-fold activation of caspase-3 in Molt-4 and 5-fold activation in HL-60 cells. Also caspases-8 and -9 were activated in HL-60 cells. Ascorbate suppressed the enhanced caspases activities indicating a pro-oxidant effect of AP9-cd. Further, caspase-3 activation correlated with NO generation that was partially impaired by nitric oxide synthase (NOS) inhibitors and ascorbate suggesting a role of pro-oxidant species in caspase-3 activation. AP9-cd produced no cytotoxicity in primary rat hepatocyte culture at the concentrations used. The studies indicated that AP9-cd mediated early NO formation leads to caspases activation, peroxide generation, and mitochondrial depolarization which may be responsible for mitochondrial-dependent and -independent apoptotic pathways involved in the killing of leukemia cells by AP9-cd.
AP9-cd是一种来自喜马拉雅雪松的标准化木脂素成分,由(-)-维克斯特罗尔、(-)-罗汉松脂素和二苄基丁内酯组成,先前报道其在多种人类癌细胞系中具有细胞毒性。本研究试图探究其在人白血病Molt-4和HL-60细胞中的细胞死亡机制。它以约15微克/毫升的48小时半数抑制浓度(IC50)抑制Molt-4细胞增殖,增加亚G0期细胞比例且无有丝分裂阻滞,产生凋亡小体并诱导DNA梯带形成。对膜联蛋白V-异硫氰酸荧光素/碘化丙啶染色细胞进行流式细胞术分析显示,凋亡及凋亡后坏死呈时间依赖性增加。所有这些生物学终点均表明细胞通过凋亡死亡。此外,初始事件包括在4小时内大量形成一氧化氮(NO),随后细胞中出现过氧化物;使用特异性荧光探针通过流式细胞术进行检测。持续高水平的NO和过氧化物似乎会降低线粒体膜电位(Ψmt),环孢素A可使Molt-4细胞中的该电位恢复。AP9-cd在Molt-4细胞中使半胱天冬酶-3激活2倍,在HL-60细胞中激活5倍。此外,HL-60细胞中的半胱天冬酶-8和-9也被激活。抗坏血酸抑制了增强的半胱天冬酶活性,表明AP9-cd具有促氧化作用。此外,半胱天冬酶-3激活与NO生成相关,一氧化氮合酶(NOS)抑制剂和抗坏血酸可部分削弱该相关性,提示促氧化物质在半胱天冬酶-3激活中起作用。在所使用的浓度下,AP9-cd在原代大鼠肝细胞培养中未产生细胞毒性。研究表明,AP9-cd介导的早期NO形成导致半胱天冬酶激活、过氧化物生成和线粒体去极化,这可能是AP9-cd杀伤白血病细胞所涉及的线粒体依赖性和非依赖性凋亡途径的原因。