Chávez Edmundo, Rodríguez José S, García Gerardo, García Noemí, Correa Francisco
Departamento de Bioquímica, Instituto Nacional de Cardiología, Ignacio Chávez, México, D.F. 014080, México.
Cell Biol Int. 2005 Jul;29(7):551-8. doi: 10.1016/j.cellbi.2005.03.009.
The purpose of this work was to assess the effect of oligomycin on the mitochondrial membrane permeability transition. The antibiotic was found to strengthen cyclosporin A (CSA)-induced protection of non-specific permeability, which is triggered by a matrix Ca2+ load in the absence of ADP. Oligomycin also reinforced the protective effect of CSA on carboxyatractyloside-induced pore opening in the absence of ADP, but failed to do so in mitochondria incubated under anaerobic conditions or after addition of CCCP. Analyzing the efflux of matrix Ca2+, we found that mitochondrial swelling and the collapse of the transmembrane electric gradient coincided with membrane leakage. The effects of the antibiotic were observed in phosphate-containing media but not in the presence of acetate. Furthermore, N-ethylmaleimide hindered the protective effect of oligomycin-CSA. In addition, the matrix phosphate concentration increased concurrently with a diminution in the matrix-free fraction of Ca2+. We concluded that oligomycin increases phosphate uptake by stimulating the phosphate-/OH- exchange reaction.
这项工作的目的是评估寡霉素对线粒体膜通透性转换的影响。发现该抗生素可增强环孢菌素A(CSA)诱导的对非特异性通透性的保护作用,这种通透性在无ADP的情况下由基质Ca2+负荷触发。寡霉素还增强了CSA对在无ADP情况下羧基苍术苷诱导的孔开放的保护作用,但在厌氧条件下孵育的线粒体或添加CCCP后则未能如此。分析基质Ca2+的外流,我们发现线粒体肿胀和跨膜电势梯度的崩溃与膜泄漏同时发生。在含磷酸盐的培养基中观察到了该抗生素的作用,但在有乙酸盐存在时则未观察到。此外,N-乙基马来酰亚胺阻碍了寡霉素-CSA的保护作用。另外,基质磷酸盐浓度随着Ca2+的无基质部分的减少而同时增加。我们得出结论,寡霉素通过刺激磷酸盐/OH-交换反应增加磷酸盐摄取。