How to clean the dirtiest place in the cell: Cationic antioxidants as intramitochondrial ROS scavengers

被引:65
作者
Skulachev, VP [1 ]
机构
[1] Moscow MV Lomonosov State Univ, Sch Bioengn & Bioinformat, Moscow 119992, Russia
[2] Moscow MV Lomonosov State Univ, Belozersky Inst Physicochem Biol, Moscow 119992, Russia
关键词
reactive oxygen species; mitochondria; MitoQ; apoptosis;
D O I
10.1080/15216540500092161
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Membrane-penetrating triphenyl alkyl phosphonium cations have been suggested for many years in our group as having the ability to measure mitochondrial potential were recently used by Murphy as vehicles to specifically target CoQ to mitochondria. As was shown in our group, the phosphonium derivative of CoQ (MitoQ) easily penetrates a planar bilayer phospholipid membrane as a cation, generating 60 mV electric potential (Delta Psi) per a 10-fold MitoQ gradient. This means that MitoQ should be unequally distributed across the inner mitochondrial membrane, the intramitochondrial [MitoQ] = extramitochondrial [MitoQ1 x 10(3) at 180 mV Delta Psi. In line with such a calculation, Murphy and his colleagues reported that antioxidant efficiency of MitoQ added to mitochondria or cells appears to be very much higher than of CoQ. It was found that H2O2-induced apoptosis (Murphy) and the H2O2-mediated bystander killing of the cultivated cells (our group) are completely arrested by pretreatement of the cells with 10(-10)-10(-8) M MitoQ. These effects indicate that MitoQ and similar compounds may be promising in treatment of heart attack, stroke and other diseases accompanied by massive apoptosis in the injured tissue. The very fact that: (i) MitoQ is not only accumulated by mitochondria but also can be regenerated in its reduced form by mitochondrial respiratory chain, (ii) it is the mitochondrial interior that produces a large portion of reactive oxygen species (ROS) in our body, and (iii) the most sensitive ROS targets are localized in the mitochondrial matrix suggest the MitoQ-like compounds are promising tools of molecular therapy of aerobic cells. In line with this suggestion, we found that addition of MitoQ strongly improves structural and biochemical parameters of cultivated cells. As to cationic tetrapeptides, recently advertised as mitochondrially-targeted Delta Psi-independent antioxidants, their effect is most probably mediated by. an opioid activity inherent in some of these substances.
引用
收藏
页码:305 / 310
页数:6
相关论文
共 33 条
[1]   Fine-tuning the hydrophobicity of a mitochondria-targeted antioxidant [J].
Asin-Cayuela, J ;
Manas, ARB ;
James, AM ;
Smith, RAJ ;
Murphy, MP .
FEBS LETTERS, 2004, 571 (1-3) :9-16
[2]   Highly potent fluorescent analogues of the opioid peptide [Dmt1]DALDA [J].
Berezowska, I ;
Chung, NN ;
Lemieux, C ;
Zelent, B ;
Szeto, HH ;
Schiller, PW .
PEPTIDES, 2003, 24 (08) :1195-1200
[3]   MITOCHONDRIAL GENERATION OF HYDROGEN-PEROXIDE - GENERAL PROPERTIES AND EFFECT OF HYPERBARIC-OXYGEN [J].
BOVERIS, A ;
CHANCE, B .
BIOCHEMICAL JOURNAL, 1973, 134 (03) :707-716
[4]   Mitochondrial function is required for hydrogen peroxide-induced growth factor receptor transactivation and downstream signaling [J].
Chen, K ;
Thomas, SR ;
Albano, A ;
Murphy, MP ;
Keaney, JF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (33) :35079-35086
[5]   Acetylcholine, bradykinin, opioids, and phenylephrine, but not adenosine, trigger preconditioning by generating free radicals and opening mitochondrial KATP channels [J].
Cohen, MV ;
Yang, XM ;
Liu, GS ;
Heusch, G ;
Downey, JM .
CIRCULATION RESEARCH, 2001, 89 (03) :273-278
[6]   Effects of antioxidants on X-ray- or hyperthermia-induced apoptosis in human lymphoma U937 cells [J].
Cui, ZG ;
Kondo, T ;
Feril, LB ;
Waki, K ;
Inanami, O ;
Kuwabara, M .
APOPTOSIS, 2004, 9 (06) :757-763
[7]   Supplementation of endothelial cells with mitochondria-targeted antioxidants inhibit peroxide-induced mitochondrial iron uptake, oxidative damage, and apoptosis [J].
Dhanasekaran, A ;
Kotamraju, S ;
Kalivendi, SV ;
Matsunaga, T ;
Shang, T ;
Keszler, A ;
Joseph, J ;
Kalyanaraman, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (36) :37575-37587
[8]  
DOMNINA LV, 2004, UNPUB
[9]   Interactions of dynorphin A-(1-13) and nociceptin with cardiac D2 binding sites: Inhibition of ischemia-evoked release of noradrenaline from synaptosomal-mitochondrial fractions [J].
Dumont, M ;
Lemaire, S .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2000, 32 (08) :1567-1574
[10]   Mitochondria-targeted antioxidants protect Friedreich Ataxia fibroblasts from endogenous oxidative stress more effectively than untargeted antioxidants [J].
Jauslin, ML ;
Meier, T ;
Smith, RAJ ;
Murphy, MP .
FASEB JOURNAL, 2003, 17 (11) :1972-+