ETHANOL INFLUENCES ON THE CHICK-EMBRYO SPINAL-CORD MOTOR SYSTEM - ANALYSES OF MOTONEURON CELL-DEATH, MOTILITY, AND TARGET TROPHIC FACTOR ACTIVITY AND IN-VITRO ANALYSES OF NEUROTOXICITY AND TROPHIC FACTOR NEUROPROTECTION

被引:30
作者
HEATON, MB [1 ]
BRADLEY, DM [1 ]
机构
[1] UNIV FLORIDA,COLL MED,ALCOHOL RES CTR,GAINESVILLE,FL 32610
来源
JOURNAL OF NEUROBIOLOGY | 1995年 / 26卷 / 01期
关键词
CHICK EMBRYO; SPINAL CORD; MOTONEURONS; CELL DEATH; NEUROTROPHIC FACTORS; ETHANOL; NEUROPROTECTION; EMBRYONIC MOTILITY;
D O I
10.1002/neu.480260105
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A series of in vivo and in vitro experiments were conducted to determine the influence of prenatally administered ethanol on several aspects of the developing chick embryo spinal cord motor system. Specifically, we examined: (1) the effect of chronic ethanol administration during the natural cell death period on spinal cord motoneuron numbers; (2) the influence of ethanol on ongoing embryonic motility; (3) the effect of ethanol exposure on neurotrophic activity in motoneuron target tissue (limb bud); and (4) the responsiveness of cultured spinal cord neurons to ethanol, and the potential of target-derived neurotrophic factors to ameliorate ethanol neurotoxicity. These studies revealed the following: Chronic prenatal ethanol exposure reduces the number of motoneurons present in the lateral motor column after the cell death period [embryonic day 12 (E12)]. Ethanol tends to inhibit embryonic motility, particularly during the later stages viewed (E9-E11). Chronic ethanol exposure reduces the neurotrophic activity contained in target muscle tissue. Such diminished support could contribute to the observed motoneuron loss. Direct exposure of spinal cord neurons to ethanol decreases neuronal survival and process outgrowth in a dose-dependent manner, but the addition of target muscle extract to ethanol-containing cultures can ameliorate this ethanol neurotoxicity. These studies demonstrate ethanol toxicity in a population not previously viewed in this regard and suggest a mechanism that may be related to this cell loss (i.e., decreased neurotrophic support). (C) 1995 John Wiley & Sons, Inc.
引用
收藏
页码:47 / 61
页数:15
相关论文
共 64 条
[1]   PRENATAL ETHANOL EXPOSURE PERMANENTLY REDUCES THE NUMBER OF PYRAMIDAL NEURONS IN RAT HIPPOCAMPUS [J].
BARNES, DE ;
WALKER, DW .
DEVELOPMENTAL BRAIN RESEARCH, 1981, 1 (03) :333-340
[2]   ALCOHOL-INDUCED NEURONAL LOSS IN DEVELOPING RATS - INCREASED BRAIN-DAMAGE WITH BINGE EXPOSURE [J].
BONTHIUS, DJ ;
WEST, JR .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1990, 14 (01) :107-118
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   POSTSYNAPTIC EFFECTS OF ETHANOL AT THE FROG NEUROMUSCULAR-JUNCTION [J].
BRADLEY, RJ ;
PEPER, K ;
STERZ, R .
NATURE, 1980, 284 (5751) :60-62
[5]   GROWTH-FACTORS ATTENUATE THE CHOLINOTOXIC EFFECTS OF ETHANOL DURING EARLY NEUROEMBRYOGENESIS IN THE CHICK-EMBRYO [J].
BRODIE, C ;
KENTROTI, S ;
VERNADAKIS, A .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 1991, 9 (03) :203-213
[6]   MUSCLE-DERIVED FACTORS ENHANCE CHOLINERGIC NEURONAL EXPRESSION IN THE CHICK-EMBRYO .2. IN CULTURE STUDIES [J].
BRODIE, C ;
VERNADAKIS, A .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 1991, 9 (04) :415-426
[7]   MOTONEURONS PURIFIED BY CELL SORTING RESPOND TO 2 DISTINCT ACTIVITIES IN MYOTUBE-CONDITIONED MEDIUM [J].
CALOF, AL ;
REICHARDT, LF .
DEVELOPMENTAL BIOLOGY, 1984, 106 (01) :194-210
[8]   PURIFICATION OF EMBRYONIC RAT MOTONEURONS BY PANNING ON A MONOCLONAL-ANTIBODY TO THE LOW-AFFINITY NGF RECEPTOR [J].
CAMU, W ;
HENDERSON, CE .
JOURNAL OF NEUROSCIENCE METHODS, 1992, 44 (01) :59-70
[9]   NGF AND BFGF PROTECT RAT HIPPOCAMPAL AND HUMAN CORTICAL-NEURONS AGAINST HYPOGLYCEMIC DAMAGE BY STABILIZING CALCIUM HOMEOSTASIS [J].
CHENG, B ;
MATTSON, MP .
NEURON, 1991, 7 (06) :1031-1041
[10]  
CHURCH MW, 1990, J PHARMACOL EXP THER, V253, P192