Alcohol-mediated purkinje cell loss in the absence of hypoxemia during the third trimester in an ovine model system

被引:25
作者
West, JR
Parnell, SE
Chen, WJA
Cudd, TA
机构
[1] Texas A&M Univ, Hlth Sci Ctr, Dept Human Anat & Med Neurobiol, Coll Med, College Stn, TX 77843 USA
[2] Texas A&M Univ, Coll Vet Med, Dept Vet Physiol & Pharmacol, College Stn, TX USA
关键词
brain; cerebellum; development; fetal alcohol syndrome; sheep;
D O I
10.1097/00000374-200107000-00016
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Although the mechanisms that underlie fetal alcohol-induced neuronal loss have not been determined, hypoxia/hypoxemia has been considered a leading candidate; This study was designed to test the hypothesis that neuronal loss could occur in the developing brain in the absence of fetal hypoxemia. Methods: Three groups of pregnant sheep were used: a control group, a binge-drinking group, and a pair-fed group. The alcohol and pair-fed animals were anesthetized on day 113 of pregnancy, and the mothers and fetuses were instrumented with arterial and venous catheters. All animals were killed on day 133. Stereological cell counting techniques were used to estimate the total number of Purkinje cells in the fetal cerebellum. Results: Peak maternal and fetal blood alcohol concentrations did not produce fetal hypoxemia. Nevertheless, there was a 25% loss of Purkinje cells of the cerebellum in the alcohol-exposed fetuses compared with that in the pair-fed controls. The loss of neurons was not accompanied by microencephaly or a concomitant decrease in either cerebellar weight or volume of the fetal cerebellum. Conclusions: Neuronal loss can be observed after alcohol exposure during the third trimester equivalent in fetal sheep in the absence of alcohol-induced hypoxemia. Furthermore, cell loss in the absence of deficits in gross brain weight or regional brain volume indicates that the lack of gross brain volume deficits from magnetic resonance imaging techniques is not a reliable indication that the brain is unaffected by the alcohol exposure.
引用
收藏
页码:1051 / 1057
页数:7
相关论文
共 55 条
[1]   Alcohol-induced changes in blood gases, glucose, and lactate in pregnant and nonpregnant rats [J].
Abel, EL .
ALCOHOL, 1996, 13 (03) :281-285
[2]  
Abel EL, 1998, ALCOHOL ALCOHOLISM, V33, P411
[3]   SELECTIVE NEURONAL VULNERABILITY TO HYPOXIA INVITRO [J].
AITKEN, PG ;
SCHIFF, SJ .
NEUROSCIENCE LETTERS, 1986, 67 (01) :92-96
[4]  
AUER RN, 1989, J NEUROSCI, V9, P1641
[5]   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
[6]   EFFECT OF ETHANOL CHRONICALLY ADMINISTERED TO PREWEANLING RATS ON CEREBELLAR DEVELOPMENT - MORPHOLOGICAL-STUDY [J].
BAUERMOFFETT, C ;
ALTMAN, J .
BRAIN RESEARCH, 1977, 119 (02) :249-268
[7]   ETHANOL-INDUCED REDUCTIONS IN CEREBELLAR GROWTH OF INFANT RATS [J].
BAUERMOFFETT, C ;
ALTMAN, J .
EXPERIMENTAL NEUROLOGY, 1975, 48 (02) :378-382
[8]   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
[9]   PERMANENT NEURONAL DEFICITS IN RATS EXPOSED TO ALCOHOL DURING THE BRAIN GROWTH SPURT [J].
BONTHIUS, DJ ;
WEST, JR .
TERATOLOGY, 1991, 44 (02) :147-163
[10]  
BRONSKY PT, 1986, J CRAN GENET DEV BIO, P113