Tempel K, von Zallinger C
Institut für Pharmakologie, Toxikologie und Pharmazie, Universität München, Germany.
Z Naturforsch C J Biosci. 1997 Jul-Aug;52(7-8):466-74. doi: 10.1515/znc-1997-7-808.
Chicken embryo cells were treated with caffeine (0.5-8.0 mM) alone or combined with various chemical and physical DNA-and/or chromatin-interactive agents. Analytical procedures comprised scheduled (SDS) and unscheduled (UDS) DNA synthesis, RNA synthesis (RNS), the activities of O6-alkylguanine-DNA alkyltransferase (AT) and poly (ADP-ribose) polymerase (PARP) as well as nucleoid sedimentation. Additional investigations were done in rat thymic and splenic cells. The effect of caffeine on DNase-I activity served as an in vitro-model system. When present in the PARP-, SDS-, UDS- and RNS-assays, caffeine inhibited the corresponding tracer (14C-NAD, dT-3H, 3H-U) incorporation in a dose-dependent manner. The AT activity was slightly stimulated. At concentrations of 0.06-0.3 mM, caffeine inhibited DNase-I activity by excess substrate. No specific effects of caffeine could be shown by nucleoid sedimentation. Besides the reduced permeability of the cells to nucleic acid precursors, the results obtained with the PARP- and DNase-I assays give evidence for the formation of a DNA-caffeine adduct as a prominent mechanism of cellular caffeine effects including DNA repair inhibition.
鸡胚细胞单独用咖啡因(0.5 - 8.0 mM)处理,或与各种化学和物理的DNA及/或染色质相互作用剂联合处理。分析程序包括定时(SDS)和不定时(UDS)DNA合成、RNA合成(RNS)、O6 - 烷基鸟嘌呤 - DNA烷基转移酶(AT)和聚(ADP - 核糖)聚合酶(PARP)的活性以及核质沉降。在大鼠胸腺和脾细胞中进行了额外的研究。咖啡因对DNase - I活性的影响用作体外模型系统。当存在于PARP、SDS、UDS和RNS测定中时,咖啡因以剂量依赖性方式抑制相应示踪剂(14C - NAD、dT - 3H、3H - U)的掺入。AT活性略有刺激。在0.06 - 0.3 mM浓度下,咖啡因通过过量底物抑制DNase - I活性。核质沉降未显示出咖啡因的特异性作用。除了细胞对核酸前体的通透性降低外,PARP和DNase - I测定的结果证明形成DNA - 咖啡因加合物是细胞咖啡因效应(包括DNA修复抑制)的一个突出机制。