Abstract

The electrochemical gradient over the inner mitochondrial membrane is the driving force for cellular ATP production. For this, electrons, which are derived from succinate and NADH, are passed along the mitochondrial electron transfer chain, and the resulting energy is used to pump protons. The transport of the positively charged protons into the mitochondrial inner membrane space builds up an electric gradient mitochondrial membrane potential (ΔΨ) and a chemical gradient ΔpH. The effective proton motive force is ΔΨ −2.3·RT·ΔpH. Mitochondria are not only the central cellular producers of ATP but also a significant source of reactive oxygen species (ROS), which are formed as a consequence of electron leak from the respiratory chain. This relatively frequent event occurs when an electron, particularly at complex I, complex III, or ubiquinone, escapes from the transfer chain and reacts with oxygen. The resulting superoxide anions (O2−) are to a great extent detoxified by manganese superoxide dismutase (MnSOD), and homozygous deletion of this important antioxidative enzyme is lethal. A low transfer rate of electrons through the respiratory chain increases the ratio of reduced to oxidized compounds and therefore favors electron escape onto oxygen and thus ROS production. Because a high ΔΨ hinders proton pumping over the inner mitochondrial membrane, high ΔΨ is thought to decrease the electron transport rate through the respiratory chain, and thus to increase ROS formation. Conversely, a reduction of ΔΨ reduces mitochondrial ROS formation.1 Besides increasing the ADP-to-ATP ratio and thus the turnover of complex V, respiratory chain uncoupling compounds have been shown to lower ΔΨ. Chemical uncouplers like dinitrophenol not only massively reduce ΔΨ but also lower mitochondrial ROS formation to an extent that ROS, in the presence of an intact antioxidant defense, become virtually undetectable. Mechanistically, uncouplers, which are also abused for fat loss therapy, are lipophilic …

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.