Biochemical and Biophysical Research Communications, Vol.495, No.2, 1716-1721, 2018
Mersalyl prevents the T1(+)-induced permeability transition pore opening in the inner membrane of Ca2+-loaded rat liver mitochondria
It was earlier shown that the calcium load of rat liver mitochondria in medium containing TINO3 and KNO3 resulted in the T1(+)-induced mitochondrial permeability transition pore (MPTP) opening in the inner membrane. This opening was accompanied by an increase in swelling and membrane potential dissipation and a decrease in state 3, state 4, and 2,4-dinitrophenol-uncoupled respiration. This respiratory decrease was markedly leveled by mersalyl (MSL), the phosphate symporter (PiC) inhibitor which poorly stimulated the calcium-induced swelling, but further increased the potential dissipation. All of these effects of Ca2+ and MSL were visibly reduced in the presence of the MPTP inhibitors (ADP, N-ethylmaleimide, and cyclosporine A). High MSL concentrations attenuated the ability of ADP to inhibit the MPTP. Our data suggest that the PiC can participate in the T1(+)-induced MPTP opening in the inner membrane of Ca2+-loaded rat liver mitochondria. (C) 2017 Elsevier Inc. All rights reserved.
Keywords:TI+;Mersalyl Mitochondrial permeability transition;Mitochondrial K plus /H plus exchanger;Mitochondrial phosphate symporter;Rat liver mitochondria