Mitochondria-Targeted Small Molecule Therapeutics and Probes

被引:317
作者
Smith, Robin A. J. [2 ]
Hartley, Richard C. [3 ]
Murphy, Michael P. [1 ]
机构
[1] Wellcome Trust Res Labs, MRC Mitochondrial Biol Unit, Cambridge CB2 0XY, England
[2] Univ Otago, Dept Chem, Dunedin, New Zealand
[3] Univ Glasgow, WestCHEM Sch Chem, Ctr Chem Res Ageing, Glasgow, Lanark, Scotland
基金
英国医学研究理事会; 英国惠康基金;
关键词
SPIN TRAP; OXIDATIVE-PHOSPHORYLATION; SUPEROXIDE-DISMUTASE; ANTIOXIDANT MITOQ; REACTIVE OXYGEN; CELL-DEATH; CU-64-LABELED TRIPHENYLPHOSPHONIUM; PEPTIDE ANTIOXIDANTS; HYDROGEN-PEROXIDE; PHOSPHONIUM;
D O I
10.1089/ars.2011.3969
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
Significance: Mitochondrial function is central to a wide range of biological processes in health and disease and there is considerable interest in developing small molecules that are taken up by mitochondria and act as either probes of mitochondrial function or therapeutics in vivo. Recent Advances: Various strategies have been used to target small molecules to mitochondria, particularly conjugation to lipophilic cations and peptides, and most of the work so far has been on mitochondria-targeted antioxidants and redox probes. In vivo studies will reveal whether there are differences in the types of bioactive functionalities that can be delivered using different carriers. Critical Issues: The outstanding challenge in the area is to discover how to combine the established selective delivery to mitochondria with the specific delivery to particular organs. Future Directions: These targeting methods will be used to direct many other bioactive molecules to mitochondria and many more wider applications other than just to antioxidants can be anticipated in the future. Antioxid. Redox Signal. 15, 3021-3038.
引用
收藏
页码:3021 / 3038
页数:18
相关论文
共 165 条
[1]   Multiple Triphenylphosphonium Cations Shuttle a Hydrophilic Peptide into Mitlochondria [J].
Abu-Gosh, Shareefa E. ;
Kolvazon, Netanel ;
Tirosh, Boaz ;
Ringel, Israel ;
Yavin, Eylon .
MOLECULAR PHARMACEUTICS, 2009, 6 (04) :1138-1144
[2]   Targeting an antioxidant to mitochondria decreases cardiac ischemia-reperfusion injury [J].
Adlam, VJ ;
Harrison, JC ;
Porteous, CM ;
James, AM ;
Smith, RAJ ;
Murphy, MP ;
Sammut, IA .
FASEB JOURNAL, 2005, 19 (09) :1088-1095
[3]   OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING [J].
AMES, BN ;
SHIGENAGA, MK ;
HAGEN, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :7915-7922
[4]   Mitochondrial H2O2 emission and cellular redox state link excess fat intake to insulin resistance in both rodents and humans [J].
Anderson, Ethan J. ;
Lustig, Mary E. ;
Boyle, Kristen E. ;
Woodlief, Tracey L. ;
Kane, Daniel A. ;
Lin, Chien-Te ;
Price, Jesse W., III ;
Kang, Li ;
Rabinovitch, Peter S. ;
Szeto, Hazel H. ;
Houmard, Joseph A. ;
Cortright, Ronald N. ;
Wasserman, David H. ;
Neufer, P. Darrell .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (03) :573-581
[5]  
[Anonymous], 2002, BIOENERGETICS
[6]   Quantitation and origin of the mitochondrial membrane potential in human cells lacking mitochondrial DNA [J].
Appleby, RD ;
Porteous, WK ;
Hughes, G ;
James, AM ;
Shannon, D ;
Wei, YH ;
Murphy, MP .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 262 (01) :108-116
[7]   Mitochondria: a target for cancer therapy [J].
Armstrong, JS .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 147 (03) :239-248
[8]   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
[9]  
AZZONE GF, 1984, CURR TOP BIOENERG, V13, P1
[10]   Mitochondria, oxidants, and aging [J].
Balaban, RS ;
Nemoto, S ;
Finkel, T .
CELL, 2005, 120 (04) :483-495