Belyaeva Elena A, Emelyanova Larisa V, Korotkov Sergey M, Brailovskaya Irina V, Savina Margarita V
I.M. Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, Thorez pr. 44, Saint Petersburg 194223, Russia.
Biomed Res Int. 2014;2014:691724. doi: 10.1155/2014/691724. Epub 2014 Jun 3.
Previously we have shown that opening of the mitochondrial permeability transition pore in its low conductance state is the case in hepatocytes of the Baltic lamprey (Lampetra fluviatilis L.) during reversible metabolic depression taking place in the period of its prespawning migration when the exogenous feeding is switched off. The depression is observed in the last year of the lamprey life cycle and is conditioned by reversible mitochondrial dysfunction (mitochondrial uncoupling in winter and coupling in spring). To further elucidate the mechanism(s) of induction of the mitochondrial permeability transition pore in the lamprey liver, we used Cd(2+) and Ca(2+) plus Pi as the pore inducers. We found that Ca(2+) plus Pi induced the high-amplitude swelling of the isolated "winter" mitochondria both in isotonic sucrose and ammonium nitrate medium while both low and high Cd(2+) did not produce the mitochondrial swelling in these media. Low Cd(2+) enhanced the inhibition of basal respiration rate of the "winter" mitochondria energized by NAD-dependent substrates whereas the same concentrations of the heavy metal evoked its partial stimulation on FAD-dependent substrates. The above changes produced by Cd(2+) or Ca(2+) plus Pi in the "winter" mitochondria were only weakly (if so) sensitive to cyclosporine A (a potent pharmacological desensitizer of the nonselective pore) added alone and they were not sensitive to dithiothreitol (a dithiol reducing agent). Under monitoring of the transmembrane potential of the "spring" lamprey liver mitochondria, we revealed that Cd(2+) produced its decrease on both types of the respiratory substrates used that was strongly hampered by cyclosporine A, and the membrane potential was partially restored by dithiothreitol. The effects of different membrane permeability modulators on the lamprey liver mitochondria function and the seasonal changes in their action are discussed.
此前我们已经表明,在波罗的海七鳃鳗(Lampetra fluviatilis L.)的肝细胞中,当其在产卵前洄游期间停止外源摄食而发生可逆性代谢抑制时,线粒体通透性转换孔处于低电导状态开放。这种抑制现象出现在七鳃鳗生命周期的最后一年,是由可逆性线粒体功能障碍引起的(冬季线粒体解偶联,春季线粒体偶联)。为了进一步阐明七鳃鳗肝脏中线粒体通透性转换孔诱导的机制,我们使用镉离子(Cd(2+))和钙离子(Ca(2+))加无机磷酸盐(Pi)作为孔诱导剂。我们发现,Ca(2+)加Pi在等渗蔗糖和硝酸铵培养基中均可诱导分离的“冬季”线粒体发生高幅度肿胀,而低浓度和高浓度的Cd(2+)在这些培养基中均未引起线粒体肿胀。低浓度的Cd(2+)增强了由烟酰胺腺嘌呤二核苷酸(NAD)依赖性底物供能的“冬季”线粒体基础呼吸速率的抑制作用,而相同浓度的重金属对黄素腺嘌呤二核苷酸(FAD)依赖性底物则产生部分刺激作用。Cd(2+)或Ca(2+)加Pi在“冬季”线粒体中产生的上述变化,单独添加环孢素A(一种非选择性孔的有效药理学脱敏剂)时仅表现出微弱(如果有的话)的敏感性,并且对二硫苏糖醇(一种二硫醇还原剂)不敏感。在监测“春季”七鳃鳗肝脏线粒体的跨膜电位时,我们发现Cd(2+)对所使用的两种呼吸底物均导致其降低,这种降低被环孢素A强烈抑制,并且膜电位可被二硫苏糖醇部分恢复。讨论了不同膜通透性调节剂对七鳃鳗肝脏线粒体功能的影响及其作用的季节性变化。