DISTURBANCE OF A MITOCHONDRIAL-DNA EXPRESSION IN GERBIL HIPPOCAMPUS AFTER TRANSIENT FOREBRAIN ISCHEMIA

被引:9
作者
ABE, K
KAWAGOE, J
LEE, TH
AOKI, M
KOGURE, K
机构
[1] Department of Neurology, Institute for Brain Diseases, Tohoku University School of Medicine, Sendai
来源
MOLECULAR BRAIN RESEARCH | 1993年 / 19卷 / 1-2期
关键词
CYTOCHROME-C OXIDASE; ISCHEMIA; MITOCHONDRIAL DNA;
D O I
10.1016/0169-328X(93)90150-N
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Hippocampal CA1 neurons are the most vulnerable to transient cerebral ischemia. However, the mechanism has not been fully understood. The level of mRNA for cytochrome c oxidase subunit I (COX-I), which is encoded by mitochondrial DNA (mtDNA), progressively decreased in the hippocampal CA1 neurons of gerbils from 1 to 3 h of the reperfusion after 3.5 min of transient forebrain ischemia, and completely disappeared at 7 days. The activity of cytochrome c oxidase (COX) protein also showed the early decrease in the CA1 cells, and was followed by the reduction of the level of COX-I DNA after 2 days. However, the activity of succinic dehydrogenase (SDH), a mitochondrial enzyme that is encoded by nuclear DNA, maintained normal activity until 1 day in the CA1 cells, and significantly decreased at 7 days. These results suggest that disturbance of mitochondrial DNA expression occurred in the CA1 neurons at the early stage of reperfusion, and was aggravated in the course of time. The disturbance could cause progressive failure of energy production of the cells that eventually results in the neuronal cell death.
引用
收藏
页码:69 / 75
页数:7
相关论文
共 29 条
[11]   DISTRIBUTIONS OF HEAT-SHOCK PROTEIN-70 MESSENGER-RNAS AND HEAT-SHOCK COGNATE PROTEIN-70 MESSENGER-RNAS AFTER TRANSIENT GLOBAL-ISCHEMIA IN GERBIL BRAIN [J].
KAWAGOE, J ;
ABE, K ;
SATO, S ;
NAGANO, I ;
NAKAMURA, S ;
KOGURE, K .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1992, 12 (05) :794-801
[12]   DELAYED NEURONAL DEATH IN THE GERBIL HIPPOCAMPUS FOLLOWING ISCHEMIA [J].
KIRINO, T .
BRAIN RESEARCH, 1982, 239 (01) :57-69
[14]  
MANIATIS T, 1982, MOL CLONING LABORATO, P187
[15]   DETECTION OF DELETED MITOCHONDRIAL GENOMES IN CYTOCHROME-C OXIDASE-DEFICIENT MUSCLE-FIBERS OF A PATIENT WITH KEARNS-SAYRE SYNDROME [J].
MITA, S ;
SCHMIDT, B ;
SCHON, EA ;
DIMAURO, S ;
BONILLA, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (23) :9509-9513
[16]   EFFECTS OF PRETREATMENT WITH SUBLETHAL ISCHEMIA ON THE EXTRACELLULAR GLUTAMATE CONCENTRATIONS DURING SECONDARY ISCHEMIA IN THE GERBIL HIPPOCAMPUS EVALUATED WITH INTRACEREBRAL MICRODIALYSIS [J].
NAKATA, N ;
KATO, H ;
LIU, Y ;
KOGURE, K .
NEUROSCIENCE LETTERS, 1992, 138 (01) :86-88
[17]   EFFECT OF ISCHEMIA ON MITOCHONDRIAL METABOLISM [J].
OZAWA, K ;
SETA, K ;
ARAKI, H ;
HANDA, H .
JOURNAL OF BIOCHEMISTRY, 1967, 61 (04) :512-&
[18]   RAPID ISOLATION OF ANIMAL MITOCHONDRIAL-DNA BY ALKALINE EXTRACTION [J].
PALVA, TK ;
PALVA, ET .
FEBS LETTERS, 1985, 192 (02) :267-270
[19]   EVIDENCE FOR A DEFECT IN NADH - UBIQUINONE OXIDOREDUCTASE (COMPLEX-I) IN HUNTINGTONS-DISEASE [J].
PARKER, WD ;
BOYSON, SJ ;
LUDER, AS ;
PARKS, JK .
NEUROLOGY, 1990, 40 (08) :1231-1234
[20]   TEMPORAL PROFILE OF NEURONAL DAMAGE IN A MODEL OF TRANSIENT FOREBRAIN ISCHEMIA [J].
PULSINELLI, WA ;
BRIERLEY, JB ;
PLUM, F .
ANNALS OF NEUROLOGY, 1982, 11 (05) :491-498