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
[51]  
SMITH RG, 1986, J NEUROSCI, V6, P439
[52]   BRAIN-DERIVED NEUROTROPHIC FACTOR PROTECTS DOPAMINE NEURONS AGAINST 6-HYDROXYDOPAMINE AND N-METHYL-4-PHENYLPYRIDINIUM ION TOXICITY - INVOLVEMENT OF THE GLUTATHIONE SYSTEM [J].
SPINA, MB ;
SQUINTO, SP ;
MILLER, J ;
LINDSAY, RM ;
HYMAN, C .
JOURNAL OF NEUROCHEMISTRY, 1992, 59 (01) :99-106
[53]   CHRONIC ETHANOL ALTERS CNS CHOLINERGIC AND CEREBELLAR DEVELOPMENT IN CHICK-EMBRYOS [J].
SWANSON, DJ ;
DANIELS, H ;
MEYER, EM ;
WALKER, DW ;
HEATON, MB .
ALCOHOL, 1994, 11 (03) :187-194
[54]   DEVELOPMENTAL-CHANGES IN UNIQUE CELL-SURFACE ANTIGENS OF CHICK-EMBRYO SPINAL MOTONEURONS AND GANGLION-CELLS [J].
TANAKA, H ;
OBATA, K .
DEVELOPMENTAL BIOLOGY, 1984, 106 (01) :26-37
[55]   DEVELOPMENTAL-CHANGES IN SPINAL-CORD NEURITE-PROMOTING ACTIVITY FROM CHICK MUSCLE EXTRACTS [J].
THOMPSON, JM ;
THOMPSON, EG .
DEVELOPMENTAL BRAIN RESEARCH, 1988, 40 (01) :158-160
[56]  
TIFFANYCASTIGLI.E, 1981, NEUROSCI LETT, V26, P157
[57]   BLOOD ETHANOL LEVELS IN SOBER ALCOHOL USERS SEEN IN AN EMERGENCY ROOM [J].
URSO, T ;
GAVALER, JS ;
VANTHIEL, DH .
LIFE SCIENCES, 1981, 28 (09) :1053-1056
[58]   CHRONIC ETHANOL-CONSUMPTION REDUCES THE NEUROTROPHIC ACTIVITY IN RAT HIPPOCAMPUS [J].
WALKER, DW ;
LEE, N ;
HEATON, MB ;
KING, MA ;
HUNTER, BE .
NEUROSCIENCE LETTERS, 1992, 147 (01) :77-80
[59]   EFFECTS OF ETHANOL EXPOSURE DURING THE 3RD TRIMESTER EQUIVALENT ON NEURON NUMBER IN RAT HIPPOCAMPUS AND DENTATE GYRUS [J].
WEST, JR ;
HAMRE, KM ;
CASSELL, MD .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1986, 10 (02) :190-197
[60]  
WEST JR, 1986, ALCOHOL BRAIN DEV, P121