GLUCOCORTICOID POTENTIATION OF LEAD NEUROTOXICITY IN THE MOUSE HN9 HIPPOCAMPAL CELL-LINE

被引:8
作者
HAYES, FD
BREEN, KC
机构
[1] Department of Pharmacology and Clinical Pharmacology, University of Dundee, Ninewells Hospital, Dundee
关键词
D O I
10.1016/0887-2333(94)90162-7
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The biochemical events underlying neurobehavioural deficits following persistent low-level lead exposure during embryonic and early postnatal development remain unclear. Because glucocorticoids have previously been demonstrated to potentiate the action of certain neurotoxins, their role in low-level lead-mediated neurotoxicity was examined using a glucocorticoid-responsive immortalized hippocampal neural cell line (HN9). Low-level lead (10(-10) M) reduced the cell number by approximately 30% over a 5-day treatment period. This effect was potentiated by treatment with the synthetic glucocorticoid dexamethasone, with a 52% decrease in cell number. Lead toxicity in actively differentiating cells was also potentiated by dexamethasone. However, while neither lead nor dexamethasone alone was toxic for cells that had previously been induced to differentiate, a combination of both drugs significantly reduced cell number. These results suggest that lead is preferentially toxic in actively dividing cells and that glucocorticoids may play a role in the potentiation of the lead-induced neurotoxicity.
引用
收藏
页码:407 / 411
页数:5
相关论文
共 29 条
[1]   EFFECT OF LOW-DOSE LEAD ACETATE EXPOSURE ON THE METABOLISM OF NUCLEIC-ACIDS AND LIPIDS IN CEREBELLUM AND HIPPOCAMPUS OF RAT DURING POSTNATAL-DEVELOPMENT [J].
AGODI, A ;
VIOLA, M ;
ALBERGHINA, M ;
STELLA, AMG .
JOURNAL OF NEUROSCIENCE RESEARCH, 1990, 25 (01) :131-138
[2]   DEVELOPMENT AND PLASTICITY OF THE HIPPOCAMPAL-CHOLINERGIC SYSTEM IN NORMAL AND EARLY LEAD EXPOSED RATS [J].
ALFANO, DP ;
PETIT, TL ;
LEBOUTILLIER, JC .
DEVELOPMENTAL BRAIN RESEARCH, 1983, 10 (01) :117-124
[3]  
ANDESIRK T, 1991, NEUROTOXICOLOGY, V12, P529
[4]  
BELLINGER D, 1986, NEUROTOXICOL TERATOL, V8, P151
[5]   LONGITUDINAL ANALYSES OF PRENATAL AND POSTNATAL LEAD-EXPOSURE AND EARLY COGNITIVE-DEVELOPMENT [J].
BELLINGER, D ;
LEVITON, A ;
WATERNAUX, C ;
NEEDLEMAN, H ;
RABINOWITZ, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (17) :1037-1043
[6]   LEAD STIMULATES GOLGI SIALYLTRANSFERASE AT TIMES COINCIDENT WITH THE EMBRYONIC TO ADULT CONVERSION OF THE NEURAL CELL-ADHESION MOLECULE (N-CAM) [J].
BREEN, KC ;
REGAN, CM .
TOXICOLOGY, 1988, 49 (01) :71-76
[7]   CHRONIC LOW-LEVEL LEAD-EXPOSURE PRECOCIOUSLY INDUCES RAT GLIAL DEVELOPMENT INVITRO AND INVIVO [J].
COOKMAN, GR ;
HEMMENS, SE ;
KEANE, GJ ;
KING, WB ;
REGAN, CM .
NEUROSCIENCE LETTERS, 1988, 86 (01) :33-37
[8]   CHRONIC LOW-LEVEL LEAD-EXPOSURE IMPAIRS EMBRYONIC TO ADULT CONVERSION OF THE NEURAL CELL-ADHESION MOLECULE [J].
COOKMAN, GR ;
KING, W ;
REGAN, CM .
JOURNAL OF NEUROCHEMISTRY, 1987, 49 (02) :399-403
[9]  
CORYSLECHTA D, 1988, SCI TOTAL ENVIRON, V71, P433
[10]   HEAVY-METALS IN AMYGDALA OF RAT - ZINC, LEAD AND COPPER [J].
DANSCHER, G ;
HALL, E ;
FREDENS, K ;
FJERDINGSTAD, E ;
FJERDINGSTAD, EJ .
BRAIN RESEARCH, 1975, 94 (01) :167-172