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寡霉素通过诱导磷酸盐摄取增强环孢菌素A对线粒体通透性转换的作用。

Oligomycin strengthens the effect of cyclosporin A on mitochondrial permeability transition by inducing phosphate uptake.

作者信息

Chávez Edmundo, Rodríguez José S, García Gerardo, García Noemí, Correa Francisco

机构信息

Departamento de Bioquímica, Instituto Nacional de Cardiología, Ignacio Chávez, México, D.F. 014080, México.

出版信息

Cell Biol Int. 2005 Jul;29(7):551-8. doi: 10.1016/j.cellbi.2005.03.009.

Abstract

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.

摘要

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。

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