Cell culture models of oxidative stress and injury in the central nervous system

被引:60
作者
Aksenova, MV [1 ]
Aksenov, MY [1 ]
Mactutus, CF [1 ]
Booze, RM [1 ]
机构
[1] Univ S Carolina, Dept Psychol Physiol & Pharmacol, Program Behav Neurosci, Columbia, SC 29208 USA
关键词
cell/tissue culture; in vitro; Alzheimer's disease; Parkinson's disease; Huntington disease; HIV-associated dementia; Prion diseases; oxidative damage; brain;
D O I
10.2174/1567202052773463
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Constantly growing body of evidence suggests that hallmarks of oxidative stress are present in various central nervous system (CNS) disorders. Technological advantages in cell culturing made it possible to use neural cell/tissue cultures as experimental models for investigation of molecular mechanisms which underlie the development of oxidative stress condition, damage and adaptive responses to oxidative insults. This review is focused on the application of cell culture methodology for studies of oxidative stress condition in the brain. The review describes studies of biomarkers of oxidative stress-dependent cell damage and adaptive responses in various kinds of brain cell culture models. It discusses the use of cell/tissue culture models for elucidation of the role and pathogenesis of oxidative stress in neurodegenerative brain disorders, AIDS-associated brain pathology, drug abuse, and aging. The review underscores the importance of cell/tissue-based studies for testing of new antioxidants and development of therapeutic strategies for amelioration of oxidative damage in the CNS. The impact of new advances in gene and protein expression analysis on the cell/tissue culture-based research of oxidative stress in the CNS is also discussed.
引用
收藏
页码:73 / 89
页数:17
相关论文
共 211 条
[1]   HYPEROXIA PRODUCES NEURONAL NECROSIS IN THE RAT [J].
AHDABBARMADA, M ;
MOOSSY, J ;
NEMOTO, EM ;
LIN, MR .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1986, 45 (03) :233-246
[2]   Protein oxidation in the brain in Alzheimer's disease [J].
Aksenov, MY ;
Aksenova, MV ;
Butterfield, DA ;
Geddes, JW ;
Markesbery, WR .
NEUROSCIENCE, 2001, 103 (02) :373-383
[3]   The expression of key oxidative stress-handling genes in different brain regions in Alzheimer's disease [J].
Aksenov, MY ;
Tucker, HM ;
Nair, P ;
Aksenova, MV ;
Butterfield, DA ;
Estus, S ;
Markesbery, WR .
JOURNAL OF MOLECULAR NEUROSCIENCE, 1998, 11 (02) :151-164
[4]   Changes in thiol content and expression of glutathione redox system genes in the hippocampus and cerebellum in Alzheimer's disease [J].
Aksenov, MY ;
Markesbery, WR .
NEUROSCIENCE LETTERS, 2001, 302 (2-3) :141-145
[5]  
Aksenova MV, 1999, J NEUROSCI RES, V58, P308, DOI 10.1002/(SICI)1097-4547(19991015)58:2<308::AID-JNR11>3.0.CO
[6]  
2-#
[7]   Oxidation of cytosolic proteins and expression of creatine kinase BB in frontal lobe in different neurodegenerative disorders [J].
Aksenova, MV ;
Aksenov, MY ;
Payne, RM ;
Trojanowski, JQ ;
Schmidt, ML ;
Carney, JM ;
Butterfield, DA ;
Markesbery, WR .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 1999, 10 (02) :158-165
[8]   Analysis of the cytosolic proteome in a cell culture model of familial amyotrophic lateral sclerosis reveals alterations to the proteasome, antioxidant defenses, and nitric oxide synthetic pathways [J].
Allen, S ;
Heath, PR ;
Kirby, J ;
Wharton, SB ;
Cookson, MR ;
Menzies, FM ;
Banks, RE ;
Shaw, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :6371-6383
[9]   Nitric oxide accounts for an increased glycolytic rate in activated astrocytes through a glycogenolysis-independent mechanism [J].
Almeida, A ;
Cidad, P ;
Bolaños, JP .
BRAIN RESEARCH, 2002, 945 (01) :131-134
[10]   Oxidative signalling and inflammatory pathways in Alzheimer's disease [J].
Anderson, I ;
Adinolfi, C ;
Doctrow, S ;
Huffman, K ;
Joy, KA ;
Malfroy, B ;
Soden, P ;
Rupniak, HT ;
Barnes, JC .
NEURONAL SIGNAL TRANSDUCTION AND ALZHEIMER'S DISEASE, 2001, 67 :141-149