Multiple Effects of 2,2`,5,5`-Tetrachlorobiphenyl on Oxidative Phosphorylation in Rat Liver Mitochondria
Authors: Mildaziene V.1, 2; Nauciene Z.1, 2; Baniene R.2; Grigiene J.1
Source: Toxicological Sciences, Volume 65, Number 2, February 2002 , pp. 220-227(8)
Publisher: Oxford University Press
Abstract:
An experimental investigation of the response of the multicomponent oxidative phosphorylation system to the environmental pollutant 2,2`,5,5`-tetrachlorobiphenyl (2,2`,5,5`-TCB) was performed by modular kinetic analysis in rat liver mitochondria oxidizing succinate (+ rotenone) and glutamate + malate. This approach facilitates the analysis of a complex process by dividing it into a small number of modules, each comprising multiple enzymatic steps, and allows evaluation of changes in the kinetics of individual blocks of the complex system induced by multisite effectors. Kinetic dependencies of the respiratory subsystem, the phosphorylation subsystem, and the proton permeability of the inner membrane on the membrane potential 
were determined in the control and in the presence of 20
M 2,2`,5,5`-TCB. The toxin inhibited the rate of respiration with both substrates to a similar extent (by 2326%). We showed that 2,2`,5,5`-TCB affected the all three modules of the oxidative phosphorylation system: it inhibited both the respiratory and the phosphorylation subsystems, and increased the membrane leak. As a result, the value of 
in State 3 of mitochondria oxidizing glutamate + malate remained the same or slightly increased with succinate, indicating that in the former case the respiratory subsystem was more sensitive to 2,2`,5,5`-TCB. We explain this by the 2,2`,5,5`-TCBinduced inhibition of Complex I. Moreover, 2,2`,5,5`-TCB decreased the number of oligomycin-binding sites by 20%, caused a significant drop in the membrane potential generated by ATP hydrolysis, and inhibited activity of ATP hydrolysis in uncoupled mitochondria. Thus, we obtained evidence that at least one of the targets of 2,2`,5,5`-TCB action within the phosphorylation module was ATP synthase.
Keywords: 2,2`,5,5`-tetrachlorobiphenyl; liver mitochondria; oxidative phosphorylation; respiration; membrane potential; ATP synthase; Complex I; kinetic analysis
Document Type: Original article
Affiliations: 1: Vytautas Magnus University, Vileikos 8, 3035 Kaunas, Lithuania; and 2: Institute for Biomedical Research, Kaunas Medical University, Eiveniu 4, 3009 Kaunas, Lithuania

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