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Increase in the toxic effects of Tl + on isolated rat liver mitochondria in the presence of nonactin
Author(s) -
Korotkov Sergey M.,
Glazunov Vadim V.,
Yagodina Olga V.
Publication year - 2007
Publication title -
journal of biochemical and molecular toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.526
H-Index - 58
eISSN - 1099-0461
pISSN - 1095-6670
DOI - 10.1002/jbt.20163
Subject(s) - mitochondrion , chemistry , valinomycin , respiration , biochemistry , succinate dehydrogenase , ionophore , membrane potential , membrane , biology , anatomy
The effects of Tl + ions on isolated rat liver mitochondria were studied in the presence of nonactin, a cyclic ionophore. Nonenergized rat liver mitochondria were increasingly swollen at an elevated concentration of Tl + in the 160 mOsm medium containing 0–150 mM sucrose and 0–75 mM TlNO 3 or 0–50 mM Tl acetate. On the contrary, mitochondria in experiments with nonactin were contracted in the medium with 5–25 mM Tl + and were swollen only in the medium with 50–75 mM TlNO 3 or 50 mM Tl acetate. State 4 respiration along with swelling of succinate‐energized mitochondria followed contraction after their deenergization was further enhanced at increasing concentration of Tl acetate in a medium containing nonactin. Regardless of the presence of nonactin, State 3 and 2,4‐dinitrophenol (DNP)‐stimulated respiration and the monoamine oxidase (MAO) activity were not affected in the medium with 0–25 mM Tl acetate and sucrose. DNP‐stimulated respiration decreased and the MAO activity somewhat increased in the medium containing 50 mM Tl acetate and nonactin. Uptake of 86 Rb + by energized mitochondria in the presence of valinomycin was considerably decreased when Tl + and nonactin were simultaneously present in the medium. An increase of the toxic effect of Tl + on rat liver mitochondria in the presence of nonactin is accounted for by disruption of mitochondria due to their more extensive swelling and uncoupling of mitochondria, resulting in the stimulation of State 4 and depletion of their energy store. © 2007 Wiley Periodicals, Inc. J Biochem Mol Toxicol 21:81–91, 2007; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/jbt.20163

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