In vitro modulation of heavy metal-induced rat liver mitochondria dysfunction: A comparison of copper and mercury with cadmium

被引:75
作者
Belyaeva, Elena A. [1 ,2 ]
Korotkov, Sergey M. [1 ]
Saris, Nils-Erik [2 ]
机构
[1] IM Sechenov Inst Evolutionary Physiol & Biochem R, St Petersburg 194223, Russia
[2] Univ Helsinki, Dept Food & Environm Sci, FIN-00014 Helsinki, Finland
基金
俄罗斯基础研究基金会;
关键词
Copper; Mercury; Cadmium; Rat liver mitochondria; Mitochondrial dysfunction mechanisms; PERMEABILITY TRANSITION PORE; RESPIRATORY-CHAIN; OXIDATIVE STRESS; ION-TRANSPORT; CD2+; TOXICITY; CALCIUM; ACTIVATION; INVOLVEMENT; SITES;
D O I
10.1016/j.jtemb.2010.10.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Cadmium (Cd), mercury (Hg) and copper (Cu) are very toxic environmental pollutants that exert their cytotoxic effects as cations by targeting mitochondria. To further underscore molecular mechanism(s) underlying the heavy metal-induced mitochondrial dysfunction we continued to compare the action of Cd, Hg and Cu using a simple and convenient in vitro model, namely isolated rat liver mitochondria incubated in assay media of different ionic contents and energized by respiratory substrates, glutamate plus malate for complex I, succinate plus rotenone for complex II, and ascorbate plus tetramethylphenylenediamine for complex IV. With the help of various selective electrodes, fluorescent probes, isotope and spectrophotofluorometric techniques, significant differences were found in the modulating action of various substances affecting the activity of these respiratory chain complexes and mitochondrial Ca2+ uniporter or permeability transition pore effectors on the mitochondrial function disturbed by the heavy metals, including clear-cut substrate specificity of many effects of these cations. Sequence of events manifested in the mitochondrial dysfunction produced by the metals under test was elucidated. (C) 2010 Elsevier GmbH. All rights reserved.
引用
收藏
页码:S63 / S73
页数:11
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