CULTURED HIPPOCAMPAL-NEURONS FROM TRISOMY 16 MOUSE, A MODEL FOR DOWNS-SYNDROME, HAVE AN ABNORMAL ACTION-POTENTIAL DUE TO A REDUCED INWARD SODIUM CURRENT

被引:48
作者
GALDZICKI, Z
COAN, E
RAPOPORT, SI
机构
[1] Laboratory of Neurosciences, National Institute on Aging, National Institutes of Health, Bethesda, MD
关键词
TRISOMY; 16; DOWNS SYNDROME; ACTION POTENTIAL; CURRENT; HIPPOCAMPUS; PRIMARY CULTURE; MOUSE; PATCH-CLAMP;
D O I
10.1016/0006-8993(93)90353-O
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mouse trisomy 16 is an animal model for Down's syndrome (human trisomy 21). The whole-cell patch-clamp technique was used to compare passive and active electrical properties of trisomy 16 and diploid mouse 16 fetal hippocampal neurons maintained in culture for 2-5 weeks. There was no significant difference in any mean passive property, including resting potential, membrane resistance, capacitance and time constant. However, in trisomic neurons, the action potential had a 20% significantly slower rising phase and a 20% significantly smaller inward sodium current and inward sodium conductance than did control neurons. The outward conductance was not altered. The ratio of maximum inward conductance to maximum outward conductance was 30% less in the trisomy 16 cells. These results indicate that trisomy 16 hippocampal neurons have abnormal active electrical properties, most likely reflecting reduced sodium channel membrane density. Such subtle differences may influence elaboration of the hippocampus during development.
引用
收藏
页码:69 / 78
页数:10
相关论文
共 51 条
[1]   NEUROPHYSIOLOGICAL ABNORMALITIES IN CULTURED DORSAL-ROOT GANGLION NEURONS FROM THE TRISOMY-16 MOUSE FETUS, A MODEL FOR DOWN SYNDROME [J].
AULT, B ;
CAVIEDES, P ;
RAPOPORT, SI .
BRAIN RESEARCH, 1989, 485 (01) :165-170
[2]   ELECTROPHYSIOLOGICAL ANALYSIS OF CULTURED FETAL MOUSE DORSAL-ROOT GANGLION NEURONS TRANSGENIC FOR HUMAN SUPEROXIDE DISMUTASE-1, A GENE IN THE DOWN SYNDROME REGION OF CHROMOSOME-21 [J].
AULT, B ;
CAVIEDES, P ;
HIDALGO, J ;
EPSTEIN, CJ ;
RAPOPORT, SI .
BRAIN RESEARCH, 1989, 497 (01) :191-194
[3]   RAT HIPPOCAMPAL NEURONS IN DISPERSED CELL-CULTURE [J].
BANKER, GA ;
COWAN, WM .
BRAIN RESEARCH, 1977, 126 (03) :397-425
[4]   GENOMIC IMPRINTING - NORMAL COMPLEMENTATION OF MURINE CHROMOSOME-16 [J].
BERGER, CN ;
EPSTEIN, CJ .
GENETICAL RESEARCH, 1989, 54 (03) :227-230
[5]  
BERNARDO LS, 1982, J NEUROSCI, V2, P1614
[6]   INACTIVATION OF SODIUM CHANNEL .1. SODIUM CURRENT EXPERIMENTS [J].
BEZANILLA, F ;
ARMSTRONG, CM .
JOURNAL OF GENERAL PHYSIOLOGY, 1977, 70 (05) :549-566
[7]   PASSIVE ELECTRICAL CONSTANTS IN 3 CLASSES OF HIPPOCAMPAL-NEURONS [J].
BROWN, TH ;
FRICKE, RA ;
PERKEL, DH .
JOURNAL OF NEUROPHYSIOLOGY, 1981, 46 (04) :812-827
[8]  
BROWN TH, 1990, ANNU REV NEUROSCI, V13, P475, DOI 10.1146/annurev.ne.13.030190.002355
[9]   EFFECTS OF NERVE GROWTH-FACTOR ON ELECTRICAL MEMBRANE-PROPERTIES OF CULTURED DORSAL-ROOT GANGLIA NEURONS FROM NORMAL AND TRISOMY-21 HUMAN FETUSES [J].
CAVIEDES, P ;
KOISTINAHO, J ;
AULT, B ;
RAPOPORT, SI .
BRAIN RESEARCH, 1991, 556 (02) :285-291
[10]   ELECTRICAL MEMBRANE-PROPERTIES OF CULTURED DORSAL-ROOT GANGLION NEURONS FROM TRISOMY-19 MOUSE FETUSES - A COMPARISON WITH THE TRISOMY-16 MOUSE FETUS, A MODEL FOR DOWN SYNDROME [J].
CAVIEDES, P ;
AULT, B ;
RAPOPORT, SI .
BRAIN RESEARCH, 1990, 511 (01) :169-172