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
  • [1] Abdelhaleem M, 2002, ANTICANCER RES, V22, P177
  • [2] Paclitaxel targets mitochondria upstream of caspase activation in intact human neuroblastoma cells
    André, N
    Carré, M
    Brasseur, G
    Pourroy, B
    Kovacic, H
    Briand, C
    Braguer, D
    [J]. FEBS LETTERS, 2002, 532 (1-2) : 256 - 260
  • [3] BEHR JP, 2000, NATO SCI SERIES TARG, P76
  • [4] RHODAMINE-123 SELECTIVELY REDUCES CLONAL GROWTH OF CARCINOMA-CELLS INVITRO
    BERNAL, SD
    LAMPIDIS, TJ
    SUMMERHAYES, IC
    CHEN, LB
    [J]. SCIENCE, 1982, 218 (4577) : 1117 - 1119
  • [5] Bisaglia M, 2000, J NEUROCHEM, V74, P1197
  • [6] A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE
    BOUSSIF, O
    LEZOUALCH, F
    ZANTA, MA
    MERGNY, MD
    SCHERMAN, D
    DEMENEIX, B
    BEHR, JP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) : 7297 - 7301
  • [7] BROWN GC, 1999, MITOCHONDRIA CELL DE, P7
  • [8] SYNTHESIS AND CHARACTERIZATION OF THIOBUTYLTRIPHENYLPHOSPHONIUM BROMIDE, A NOVEL THIOL REAGENT TARGETED TO THE MITOCHONDRIAL MATRIX
    BURNS, RJ
    SMITH, RAJ
    MURPHY, MP
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 322 (01) : 60 - 68
  • [9] Labeling of mitochondrial proteins in living cells by the thiol probe thiobutyltriphenylphosphonium bromide
    Burns, RJ
    Murphy, MP
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 339 (01) : 33 - 39
  • [10] CHEN LB, 1988, ANNU REV CELL BIOL, V4, P155, DOI 10.1146/annurev.cellbio.4.1.155