Barham S S, Brinkley B R
Cytobios. 1976;15(58-59):85-96.
Inhibitors of mitochondrial respiration, phosphorylation inhibitors, and uncoupling agents have been reported to delay or inhibit mitosis in cultured mammalian cells. Although the molecular mechanism by which mitosis is delayed in the presence of most respiratory inhibitors presumably involves lowered ATP production for mitotic requirements, one respiratory inhibitor, rotenone, was determined to arrest mitosis by an unrelated mechanism. Cell cycle kinetics studies, oxygen consumption measurements, and viscosity assays indicate that rotenone arrests cultured mammalian cells in mitosis by inhibiting spindle microtubule assembly by a mechanism analogous with colchicine, Colecemid and related antimitotic drugs. Amytal, which blocks electron transport at the same site as does rotenone, failed to arrest cell progression at mitosis. Rotenone delayed cell progression in all phases of the cell cycle, apparently as a direct result of respiration inhibition. Thus, rotenone appears to exert a dual function on events of the cell cycle.
据报道,线粒体呼吸抑制剂、磷酸化抑制剂和解偶联剂可延缓或抑制培养的哺乳动物细胞的有丝分裂。尽管在大多数呼吸抑制剂存在的情况下,有丝分裂延迟的分子机制可能涉及为有丝分裂需求而降低的ATP产生,但有一种呼吸抑制剂鱼藤酮被确定是通过一种不相关的机制来阻止有丝分裂的。细胞周期动力学研究、氧气消耗测量和粘度测定表明,鱼藤酮通过抑制纺锤体微管组装,以类似于秋水仙碱、秋水仙酰胺和相关抗有丝分裂药物的机制,使培养的哺乳动物细胞在有丝分裂中停滞。阿米妥在与鱼藤酮相同的位点阻断电子传递,但未能使细胞在有丝分裂时停止进程。鱼藤酮使细胞周期的所有阶段的细胞进程延迟,显然是呼吸抑制的直接结果。因此,鱼藤酮似乎对细胞周期事件发挥双重作用。