Mitochondrial metabolic states and membrane potential modulate mtNOS activity

• Published in: Biochimica et biophysica acta 2006-03, Vol.1757 (3), p.166-172
• Main Authors: Valdez, Laura B., Zaobornyj, Tamara, Boveris, Alberto
• Format: Article
• Language: English
• Subjects: Animals; Female; Hydrogen-Ion Concentration; Membrane Potentials; Mitochondria - enzymology; Mitochondria - metabolism; Mitochondrial membrane potential; Mitochondrial Membranes - metabolism; Mitochondrial NO; mtNOS; Nitric Oxide - metabolism; Nitric Oxide Synthase - metabolism; NO release; Oxidation-Reduction; Oxygen - metabolism; Rats; Rats, Sprague-Dawley; State 4–state 3 transition; Voltage-dependent enzyme activity
• ISSN: 0005-2728; 0006-3002; 1879-2650
• DOI: 10.1016/j.bbabio.2006.02.013

The mitochondrial metabolic state regulates the rate of NO release from coupled mitochondria: NO release by heart, liver and kidney mitochondria was about 40–45% lower in state 3 (1.2, 0.7 and 0.4 nmol/min mg protein) than in state 4 (2.2, 1.3 and 0.7 nmol/min mg protein). The activity of mtNOS, responsible for NO release, appears driven by the membrane potential component and not by intramitochondrial pH of the proton motive force. The intramitochondrial concentrations of the NOS substrates, l-arginine (about 310 μM) and NADPH (1.04–1.78 mM) are 60–1000 times higher than their K M values. Moreover, the changes in their concentrations in the state 4–state 3 transition are not enough to explain the changes in NO release. Nitric oxide release was exponentially dependent on membrane potential as reported for mitochondrial H 2O 2 production [S.S. Korshunov, V.P. Skulachev, A.A. Satarkov, High protonic potential actuates a mechanism of production of reactive oxygen species in mitochondria. FEBS Lett. 416 (1997) 15–18.]. Agents that decrease or abolish membrane potential minimize NO release while the addition of oligomycin that produces mitochondrial hyperpolarization generates the maximal NO release. The regulation of mtNOS activity, an apparently voltage-dependent enzyme, by membrane potential is marked at the physiological range of membrane potentials.