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On the Mechanism(s) of Membrane Permeability Transition in Liver Mitochondria of Lamprey Lampetra fluviatilis L.: Insights from Cadmium

机译:关于南美洲兰Lamp(Lanetra fluviatilis L.)肝线粒体膜通透性转变的机制:镉的见解

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摘要

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 Cd2+ and Ca2+ plus Pi as the pore inducers. We found that Ca2+ 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 Cd2+ did not produce the mitochondrial swelling in these media. Low Cd2+ 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 Cd2+ or Ca2+ 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 Cd2+ 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.
机译:先前我们已经证明,在低传导状态下线粒体通透性过渡孔的开放是在外源性进食时其产卵前迁移期间可逆代谢抑制期间发生的波罗的海七rey(Lampetra fluviatilis L.)肝细胞中的情况。关闭。抑郁症在七lamp鳗生命周期的最后一年中观察到,并由可逆的线粒体功能障碍(冬季的线粒体解偶联和春季的偶联)调节。为了进一步阐明在七rey鳗肝脏中线粒体通透性过渡孔的诱导机制,我们使用Cd 2 + 和Ca 2 + 加Pi作为孔诱导剂。我们发现Ca 2 + 加上Pi在等渗蔗糖和硝酸铵介质中诱导了孤立的“冬季”线粒体的高幅度溶胀,而Cd 2 + 在这些培养基中未产生线粒体肿胀。低Cd 2 + 增强了NAD依赖性底物激发的“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引起FAD依赖性底物上的部分刺激。 Cd 2 + 或Ca 2 + 加Pi在“冬季”线粒体中产生的上述变化仅对环孢霉素A(一种有效的药理脱敏剂)敏感(如果有的话)单独添加的非选择性孔中的一部分),它们对二硫苏糖醇(一种二硫醇还原剂)不敏感。在监测“春季”七lamp鳗肝线粒体跨膜电位的过程中,我们发现Cd 2 + 在使用的两种呼吸底物上均产生了下降,而这两种底物均受到环孢菌素A和膜的强烈阻碍二硫苏糖醇可部分恢复电位。讨论了不同的膜通透性调节剂对七lamp鳗肝脏线粒体功能的影响及其作用的季节性变化。

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