Saha Biswarup, Mukherjee Ananda, Samanta Saheli, Saha Piyali, Ghosh Anup Kumar, Santra Chitta Ranjan, Karmakar Parimal
Department of Life Science and Biotechnology, Jadavpur University, Kolkata 700 032, West Bengal, India.
Toxicol In Vitro. 2009 Sep;23(6):1100-9. doi: 10.1016/j.tiv.2009.05.018. Epub 2009 May 31.
Combined effects of alprazolam (Alp), a member of benzodiazepine group of drugs and caffeine on human cell lines, HeLa and THP1 were investigated in this study. Alp mediated cytotoxicity was enhanced while caffeine was present. The cell death was confirmed by observing morphological changes, LDH assay and membrane anisotropic study. Also such combined effects induced elevated level of ROS and depletion of GSH. The mechanism of cell death induced by simultaneous treatment of Alp and caffeine was associated with the calcium-mediated activation of mu-calpain, release of lysosomal protease cathepsin B, activation of PARP and cleavage of caspase 3. Our results indicate that, Alp alone induces apoptosis in human cells but in the presence of caffeine it augments necrosis in a well-regulated pathway. Thus our observations strongly suggest that, alprazolam and caffeine together produce severe cytotoxicity in human cell lines.
本研究调查了苯二氮䓬类药物阿普唑仑(Alp)与咖啡因对人细胞系HeLa和THP1的联合作用。当存在咖啡因时,阿普唑仑介导的细胞毒性增强。通过观察形态变化、乳酸脱氢酶(LDH)测定和膜各向异性研究证实了细胞死亡。此外,这种联合作用导致活性氧(ROS)水平升高和谷胱甘肽(GSH)消耗。同时用阿普唑仑和咖啡因处理诱导细胞死亡的机制与钙介导的μ-钙蛋白酶激活、溶酶体蛋白酶组织蛋白酶B释放、聚(ADP-核糖)聚合酶(PARP)激活和半胱天冬酶3裂解有关。我们的结果表明,单独使用阿普唑仑可诱导人细胞凋亡,但在咖啡因存在的情况下,它会通过一条调控良好的途径加剧坏死。因此,我们的观察结果强烈表明,阿普唑仑和咖啡因共同作用会在人细胞系中产生严重的细胞毒性。