Mitochondrial pharmaceutics

被引:83
作者
Weissig, V [1 ]
Cheng, SM [1 ]
D'Souza, GGM [1 ]
机构
[1] Northeastern Univ, Dept Pharmaceut Sci, Sch Pharm, Bouve Coll Hlth Sci, Boston, MA 02115 USA
关键词
mitochondria; drug delivery; mitochondrial gene therapy; mitochondrial drug targeting; intracellular drug delivery; subcellular targeting;
D O I
10.1016/j.mito.2003.11.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Since the end of the 1980s, key discoveries have been made which have significantly revived the scientific interest in a cell organelle, which has been studied continuously and with steady success for the last 100 years. It has become increasingly evident that mitochondrial dysfunction contributes to a variety of human disorders, ranging from neurodegenerative and neuromuscular diseases, obesity, and diabetes to ischemia-reperfusion injury and cancer. Moreover, since the middle of the '1990s, mitochondria, the 'power house' of the cell, have also become accepted as the cell's 'arsenals' reflecting their increasingly acknowledged key role during apoptosis. Based on these recent developments in mitochondrial research, increased pharmacological and pharmaceutical efforts have lead to the emergence of 'Mitochondrial Medicine' as a whole new field of biomedical research. Targeting of biologically active molecules to mitochondria in living cells will open up avenues for manipulating mitochondrial functions, which may result in the selective protection, repair or eradication of cells. This review gives a brief synopsis over current strategies of mitochondrial targeting and their possible therapeutic applications. (C) 2004 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
引用
收藏
页码:229 / 244
页数:16
相关论文
共 79 条
  • [31] Mitochondria transfection by oligonucleotides containing a signal peptide and vectorized by cationic liposomes
    Geromel, V
    Cao, A
    Briane, D
    Vassy, J
    Rotig, A
    Rustin, P
    Coudert, R
    Rigaut, JP
    Munnich, A
    Taillandier, E
    [J]. ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 2001, 11 (03): : 175 - 180
  • [32] Selective targeting of a redox-active ubiquinone to mitochondria within cells - Antioxidant and antiapoptotic properties
    Kelso, GF
    Porteous, CM
    Coulter, CV
    Hughes, G
    Porteous, WK
    Ledgerwood, EC
    Smith, RAJ
    Murphy, MP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (07) : 4588 - 4596
  • [33] CYTOKINETIC BEHAVIOR OF EHRLICH ASCITES TUMOR AFTER INVIVO TREATMENT WITH CIS-DIAMMINEDICHLOROPLATINUM(II) AND METALLOCENE DICHLORIDES
    KOPFMAIER, P
    WAGNER, W
    LISS, E
    [J]. JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1981, 102 (01) : 21 - 30
  • [34] Kroemer G, 1999, BIOCHEM SOC SYMP, V66, P1
  • [35] LAMPIDIS TJ, 1983, CANCER RES, V43, P716
  • [36] Revolution in mitochondrial medicine
    Larsson, NG
    Luft, R
    [J]. FEBS LETTERS, 1999, 455 (03) : 199 - 202
  • [37] Dequalinium™ vesicles form stable complexes with plasmid DNA which are protected from DNase attack
    Lasch, J
    Meye, A
    Taubert, H
    Koelsch, R
    Mansa-ard, J
    Weissig, V
    [J]. BIOLOGICAL CHEMISTRY, 1999, 380 (06) : 647 - 652
  • [38] Pharmaceutical approach to somatic gene therapy
    Ledley, FD
    [J]. PHARMACEUTICAL RESEARCH, 1996, 13 (11) : 1595 - 1614
  • [39] MECHANISM OF COUPLING OF OXIDATIVE PHOSPHORYLATION AND MEMBRANE POTENTIAL OF MITOCHONDRIA
    LIBERMAN, EA
    TOPALY, VP
    TSOFINA, LM
    JASAITIS, AA
    SKULACHEV, VP
    [J]. NATURE, 1969, 222 (5198) : 1076 - +
  • [40] Specific modification of mitochondrial protein thiols in response to oxidative stress - A proteomics approach
    Lin, TK
    Hughes, G
    Muratovska, A
    Blaikie, FH
    Brookes, PS
    Darley-Usmar, V
    Smith, RAJ
    Murphy, MP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (19) : 17048 - 17056