Reyes J, Benos D J
Membr Biochem. 1984;5(3):243-68. doi: 10.3109/09687688409150281.
The charged and uncharged forms of carbonylcyanide phenylhydrazone uncouplers bind to phosphatidylcholine monolayers in a dose-dependent fashion, inducing changes in the interfacial potential of these model membranes. The interfacial potential change produced by the charged uncoupler is composed of a double-layer potential and an internal electrostatic potential (boundary and/or dipole). Changes in double-layer potential induced by the uncouplers in mitochondrial membranes can explain both the inhibition of oxygen consumption (QO2) caused by the uncouplers and the competition shown by succinate when mitochondria are respiring in the presence of rotenone. From these results and from dose-response curves of QO2 versus uncoupler concentrations, we conclude that 1 microM is an upper limit for free uncoupler concentration in the medium to avoid unwanted side effects during cell physiology studies that require total mitochondrial uncoupling.
羰基氰化物苯腙解偶联剂的带电形式和不带电形式以剂量依赖的方式与磷脂酰胆碱单层结合,导致这些模型膜的界面电位发生变化。带电解偶联剂产生的界面电位变化由双层电位和内部静电电位(边界和/或偶极)组成。解偶联剂在线粒体内膜中诱导的双层电位变化既可以解释解偶联剂对氧消耗(QO2)的抑制作用,也可以解释当线粒体在鱼藤酮存在下进行呼吸时琥珀酸所表现出的竞争性作用。根据这些结果以及QO2与解偶联剂浓度的剂量反应曲线,我们得出结论,在需要完全线粒体解偶联的细胞生理学研究中,为避免不必要的副作用,培养基中游离解偶联剂浓度的上限为1微摩尔。