Rotenone and pyruvate prevent the tert-butylhydroperoxide-induced necrosis of U937 cells and allow them to proliferate

被引:15
作者
Sestili, P
Brambilla, L
Cantoni, O
机构
[1] Univ Urbino, Ist Farmacol & Farmacognosia, I-60129 Urbino, Italy
[2] Univ Urbino, Ctr Farmacol Oncol Sperimentale, I-60129 Urbino, Italy
关键词
tert-butylhydroperoxide; necrosis; mitochondrial membrane permeability transition; mitochondrial NADH;
D O I
10.1016/S0014-5793(99)01027-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Exposure of U937 cells to tert-butylhydroperoxide (tB-OOH) led to cyclosporin A-sensitive mitochondrial membrane permeability transition and necrosis, Pyruvate and rotenone, which increase mitochondrial NADH via different mechanisms, prevented these responses and the cells which received these treatments proliferated,vith kinetics similar to those observed in untreated cells. In contrast with these results, cells rescued by cyclosporin A were unable to proliferate. Thus, mitochondrial NADH plays a pivotal role in preventing upstream events which result in the onset of mitochondrial membrane permeability transition and death in cells exposed to tB-OOH. These events appear to be critical for recovery of the ability of the cells to proliferate, (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:139 / 143
页数:5
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