Korotkov S M, Skulskii I A, Glazunov V V
Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, Torez pr., Russian Federation.
J Inorg Biochem. 1998 Apr;70(1):17-23. doi: 10.1016/s0162-0134(98)00008-7.
Changes in Cd2+ effects on respiration of succinate-energized rat liver mitochondria were studied after replacement of 100 mM KCl in an incubation medium by equimolar amounts of NaCl or LiCl, or by 200 mM sucrose. In KCl medium, 2.5-10 microM Cd2+ decreased the state 3 and 2,4-dinitrophenol (DNP)-stimulated respiration of mitochondria, and increased their respiration in the state 4, however, 10-40 microM Cd2+ diminished the state 4 respiration. Compared to the experiments with KCl medium, it was demonstrated that Cd2+ effects on the mitochondrial respiration was increased in NaCl medium, decreased in sucrose medium, and unchanged in LiCl medium, except that 10-25 microM Cd2+ decreased the state 4 respiration of mitochondria in the same way as in the NaCl medium. Cd2+ (20 microM) stimulated an extensive swelling of nonenergized mitochondria incubated in 125 mM nitrate media, the effect being increased in the series of Li < Na < K < NH4. Swelling of succinate-energized mitochondria incubated in K-acetate medium was additionally stimulated by 10 microM Cd2+. The initially low swelling of succinate-energized mitochondria in the KCl medium increased with increase in Cd2+ concentrations in this medium. Differences found in the Cd2+ effects on respiration and on swelling of mitochondria incubated in the media used are discussed in terms of general ion permeabilities and differences in Cd2+ binding, its uptake, and interaction with respiratory enzymes.
在将孵育培养基中的100 mM KCl用等摩尔量的NaCl或LiCl或200 mM蔗糖替代后,研究了Cd2+对琥珀酸供能的大鼠肝线粒体呼吸作用的影响。在KCl培养基中,2.5 - 10 μM Cd2+降低了线粒体的状态3以及2,4 - 二硝基苯酚(DNP)刺激的呼吸作用,并增加了其状态4下的呼吸作用,然而,10 - 40 μM Cd2+降低了状态4下的呼吸作用。与在KCl培养基中进行的实验相比,结果表明,在NaCl培养基中Cd2+对线粒体呼吸的影响增强;在蔗糖培养基中减弱;在LiCl培养基中无变化,但10 - 25 μM Cd2+与在NaCl培养基中一样降低了线粒体状态4下的呼吸作用。20 μM Cd2+刺激了在125 mM硝酸盐培养基中孵育的非供能线粒体的广泛肿胀,在Li < Na < K < NH4系列中这种作用增强。在K - 乙酸盐培养基中孵育的琥珀酸供能线粒体肿胀可被10 μM Cd2+进一步刺激。在KCl培养基中琥珀酸供能线粒体最初较低的肿胀程度随该培养基中Cd2+浓度升高而增加。根据一般离子通透性以及Cd2+结合、摄取及其与呼吸酶相互作用方面存在的差异,对在所用培养基中孵育的线粒体上发现的Cd2+对呼吸作用和肿胀影响的差异进行了讨论。