THE QUANTITATIVE CONTRIBUTIONS OF MITOCHONDRIAL PROTON LEAK AND ATP TURNOVER REACTIONS TO THE CHANGED RESPIRATION RATES OF HEPATOCYTES FROMRATS OF DIFFERENT THYROID STATUS

Citation
Me. Harper et Md. Brand, THE QUANTITATIVE CONTRIBUTIONS OF MITOCHONDRIAL PROTON LEAK AND ATP TURNOVER REACTIONS TO THE CHANGED RESPIRATION RATES OF HEPATOCYTES FROMRATS OF DIFFERENT THYROID STATUS, The Journal of biological chemistry, 268(20), 1993, pp. 4850-4860
Citations number
56
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
268
Issue
20
Year of publication
1993
Pages
4850 - 4860
Database
ISI
SICI code
0021-9258(1993)268:20<4850:TQCOMP>2.0.ZU;2-Q
Abstract
Hepatocytes from hypothyroid rats respire more slowly than those from control animals; cells from hyperthyroid rats respire faster. We have identified the blocks of reactions whose kinetics are significantly af fected by thyroid hormones and have quantified the contribution of flu x through different blocks of energy-dissipating reactions to the alte red oxygen consumption. In cells from hypothyroid rats compared with l ittermate euthyroid controls, there were significant kinetic effects o n non-mitochondrial oxygen consumption reactions and on mitochondrial proton leak but not on ATP turnover. Approximately 50% of the decrease in cellular oxygen consumption of hypothyroid cells was accounted for by a decrease in mitochondrial proton leak rate and approximately 50% by decreased non-mitochondrial oxygen consumption. Metabolic control analysis showed that the distribution of control over oxidative phosph orylation and mitochondrial potential in hepatocytes from hypothyroid animals was broadly similar to its distribution in euthyroid controls. In cells from hyperthyroid rats compared with littermate euthyroid co ntrols, there were significant kinetic effects on mitochondrial proton leak and on the reactions involved in ATP synthesis and consumption b ut not on non-mitochondrial oxygen consumption. Approximately 50% of t he increase in cellular oxygen consumption in hyperthyroid cells was a ccounted for by an increased mitochondrial proton leak rate and the re mainder by increased ATP turnover; there were no changes in non-mitoch ondrial oxygen consumption.