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Mitochondria-targeted plastoquinone derivatives as tools to interrupt execution of the aging program. 1. Cationic plastoquinone derivatives: Synthesis and in vitro studies
Authors:Y N Antonenko  A V Avetisyan  L E Bakeeva  B V Chernyak  V A Chertkov  L V Domnina  O Yu Ivanova  D S Izyumov  L S Khailova  S S Klishin  G A Korshunova  K G Lyamzaev  M S Muntyan  O K Nepryakhina  A A Pashkovskaya  O Yu Pletjushkina  A V Pustovidko  V A Roginsky  T I Rokitskaya  E K Ruuge  V B Saprunova  I I Severina  R A Simonyan  I V Skulachev  M V Skulachev  N V Sumbatyan  I V Sviryaeva  V N Tashlitsky  J M Vassiliev  M Yu Vyssokikh  L S Yaguzhinsky  A A Zamyatnin Jr  V P Skulachev
Institution:1. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119991, Moscow, Russia
2. Chemical Faculty, Lomonosov Moscow State University, 119991, Moscow, Russia
3. Institute of Chemical Physics, ul. Kosygina 4, 119977, Moscow, Russia
4. Institute of Experimental Cardiology, Cardiology Research Center, 3-ya Cherepkovskaya ul. 15A, 121552, Moscow, Russia
5. Biological Faculty, Lomonosov Moscow State University, 119991, Moscow, Russia
6. Mitoengineering Center, Lomonosov Moscow State University, 119991, Moscow, Russia
7. Faculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, 119991, Moscow, Russia
Abstract:Synthesis of cationic plastoquinone derivatives (SkQs) containing positively charged phosphonium or rhodamine moieties connected to plastoquinone by decane or pentane linkers is described. It is shown that SkQs (i) easily penetrate through planar, mitochondrial, and outer cell membranes, (ii) at low (nanomolar) concentrations, posses strong antioxidant activity in aqueous solution, BLM, lipid micelles, liposomes, isolated mitochondria, and cells, (iii) at higher (micromolar) concentrations, show pronounced prooxidant activity, the “window” between anti- and prooxidant concentrations being very much larger than for MitoQ, a cationic ubiquinone derivative showing very much lower antioxidant activity and higher prooxidant activity, (iv) are reduced by the respiratory chain to SkQH2, the rate of oxidation of SkQH2 being lower than the rate of SkQ reduction, and (v) prevent oxidation of mitochondrial cardiolipin by OH·. In HeLa cells and human fibroblasts, SkQs operate as powerful inhibitors of the ROS-induced apoptosis and necrosis. For the two most active SkQs, namely SkQ1 and SkQR1, C 1/2 values for inhibition of the H2O2-induced apoptosis in fibroblasts appear to be as low as 1·10−11 and 8·10−13 M, respectively. SkQR1, a fluorescent representative of the SkQ family, specifically stains a single type of organelles in the living cell, i.e. energized mitochondria. Such specificity is explained by the fact that it is the mitochondrial matrix that is the only negatively-charged compartment inside the cell. Assuming that the Δψ values on the outer cell and inner mitochondrial membranes are about 60 and 180 mV, respectively, and taking into account distribution coefficient of SkQ1 between lipid and water (about 13,000: 1), the SkQ1 concentration in the inner leaflet of the inner mitochondrial membrane should be 1.3·108 times higher than in the extracellular space. This explains the very high efficiency of such compounds in experiments on cell cultures. It is concluded that SkQs are rechargeable, mitochondria-targeted antioxidants of very high efficiency and specificity. Therefore, they might be used to effectively prevent ROS-induced oxidation of lipids and proteins in the inner mitochondrial membrane in vivo. Electronic Supplementary Material  Supplementary material is available for this article at and is accessible for authorized users. Published in Russian in Biokhimiya, 2008, Vol. 73, No. 12, pp. 1589–1606. This and the following four articles were written by the request of the Editorial Board of Biochemistry (Moscow).
Keywords:SkQ1  penetrating cations  plastoquinone  antioxidants  mitochondria  apoptosis
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