Numbers of neurons and glia in mature rat somatosensory cortex: Effects of prenatal exposure to ethanol

Stereological methods were used to examine the consequences of prenatal exposure to ethanol on the structure of area 3, primary somatosensory cortex, of the mature hooded rat. Pregnant rats were fed a liquid diet containing 6.7% (v/v) ethanol (Et), pairfed an isocaloric liquid control diet (Ct), or fed a diet of chow and water (Ch). Cresyl violet‐stained sections of 3‐month‐old pups were examined. The corrected mean size of the cell bodies of neurons in layers other than layer V was significantly smaller in the Ettreated rats; conversely, the mean somatic size of glia in each layer was significantly larger in the Ettreated rats. The laminar cell packing density for neurons and glia, however, was similar in rats from both treatment groups. The overall volume of area 3 and the volume of individual layers were about 33% smaller in Et‐treated rats than in the pair‐fed controls. Thus, the estimated total number of neurons in Et‐treated rats (1.79*106) was significantly fewer than in Chtreated rats (2.77*106) and in Ct‐treated rats (2.66*106). The total number of glia also was about 30% fewer in Et‐treated rats than in the controls. Not all layers were affected equivalently. The space occupied by the neuropil was significantly greater in Et‐treated rats, but only in layers II/III, IV, and VI; hence, the cell body/neuropil ratio in these layers was less in Et‐treated rats than in the controls. Therefore, microcephaly caused by prenatal exposure to ethanol results not only from a miniaturization of the brain, but also from a permanent abnormal organization of cerebral cortex.

[1]  M. J. Elliott,et al.  Cell proliferation in the embryonic mouse neocortex following acute maternal alcohol intoxication , 1985, International Journal of Developmental Neuroscience.

[2]  M. Cassell,et al.  Effects of ethanol exposure during the third trimester equivalent on neuron number in rat hippocampus and dentate gyrus. , 1986, Alcoholism, clinical and experimental research.

[3]  C. D'amato,et al.  The development of the mammalian nervous system I. Malformations of the brain, especially the cerebral cortex, induced in rats by radiation II. Some mechanisms of the malformations of the cortex , 1959, The Journal of comparative neurology.

[4]  T. J. Cunningham,et al.  Neuron numbers in the superior cervical sympathetic ganglion of the rat: a critical comparison of methods for cell counting , 1983, Journal of neurocytology.

[5]  P. Terranova,et al.  Early motor development and cerebral cortical morphology in rats exposed perinatally to alcohol. , 1988, Alcoholism, clinical and experimental research.

[6]  D. Walker,et al.  Prenatal ethanol exposure permanently reduces the number of pyramidal neurons in rat hippocampus. , 1981, Brain research.

[7]  J. Altman,et al.  Experimental reorganization of the cerebellar cortex. II. Effects of elimination of most microneurons with prolonged x‐irradiation started at four days , 1973, The Journal of comparative neurology.

[8]  M. Spatz,et al.  QUANTITATIVE CHANGES WITH AGE IN THE DNA CONTENT OF METHYLAZOXYMETHANOL‐INDUCED MICROENCEPHALIC RAT BRAIN 1 , 1972, Journal of neurochemistry.

[9]  J. Altman,et al.  Early effects of x-irradiation of the cerebellum in infant rats: decimation and reconstitution of the external granular layer. , 1969, Experimental neurology.

[10]  Michael W. Miller,et al.  Structural and metabolic alterations in rat cerebral cortex induced by prenatal exposure to ethanol , 1988, Brain Research.

[11]  Michael W. Miller,et al.  Effects of prenatal exposure to ethanol on neocortical development: II. Cell proliferation in the ventricular and subventricular zones of the rat , 1989, The Journal of comparative neurology.

[12]  P. Patsalos,et al.  The synthesis of myelin and brain subcellular membrane proteins in the offspring of rats fed ethanol during pregnancy , 1982, Brain Research.

[13]  S. Muller,et al.  Structure and histogenesis of the principal sensory nucleus of the trigeminal nerve: Effects of prenatal exposure to ethanol , 1989, The Journal of comparative neurology.

[14]  D. Walker,et al.  Ethanol-induced malformations in mice. , 1977, Alcoholism, clinical and experimental research.

[15]  Michael W. Miller,et al.  Effect of prenatal exposure to alcohol on the distribution and time of origin of corticospinal neurons in the rat , 1987, The Journal of comparative neurology.

[16]  G. Stoltenburg‐Didinger,et al.  Fetal alcohol syndrome and mental retardation: spine distribution of pyramidal cells in prenatal alcohol-exposed rat cerebral cortex; a Golgi study. , 1983, Brain research.

[17]  J. Altman,et al.  Experimental reorganization of the cerebellar cortex. I. Morphological effects of elimination of all microneurons with prolonged x‐irradiation started at birth , 1972, The Journal of comparative neurology.

[18]  S. Wise,et al.  The motor cortex of the rat: Cytoarchitecture and microstimulation mapping , 1982, The Journal of comparative neurology.

[19]  S. Al-Rabiai,et al.  Effect of prenatal exposure to ethanol on the ultrastructure of layer V of mature rat somatosensory cortex , 1989, Journal of neurocytology.

[20]  David W. Smith,et al.  The fetal alcohol syndrome. , 1978, The Lamp.

[21]  C. Welker,et al.  Generalized growth retardation in rats induced by prenatal exposure to methylazoxymethyl acetate. , 1972, Teratology.

[22]  S. Borges,et al.  THE EFFECT OF ETHANOL ON THE CELLULAR COMPOSITION OF THE CEREBELLUM , 1983, Neuropathology and applied neurobiology.

[23]  A. Peters,et al.  The neuronal composition of area 17 of rat visual cortex. III. Numerical considerations , 1985, The Journal of comparative neurology.

[24]  J. West,et al.  Prenatal exposure to ethanol alters the organization of hippocampal mossy fibers in rats. , 1981, Science.

[25]  Control of cell number in the developing neocortex. II. Effects of corpus callosum section. , 1988, Brain research.

[26]  L. A. Kotkoskie,et al.  Prenatal brain malformations following acute ethanol exposure in the rat. , 1988, Alcoholism, clinical and experimental research.

[27]  M. Miller,et al.  Effects of alcohol on the generation and migration of cerebral cortical neurons. , 1986, Science.

[28]  D. W. Vaughan The Structure of Neuroglial Cells , 1984 .

[29]  A. Scheibel,et al.  Morphologic evidence for a delay of neuronal maturation in fetal alcohol exposure , 1981, Experimental Neurology.

[30]  J. Fleshman,et al.  Adjustment of connectivity in rat neocortex after prenatal destruction of precursor cells of layers II-IV. , 1981, Brain research.

[31]  M. Druse,et al.  Maternal ethanol consumption: Lack of effect on synaptogenesis in layer I of the motor cortex in 19-day-old rat offspring , 1986, Experimental Neurology.

[32]  A. J. Smolen Retrograde transneuronal regulation of the afferent innervation to the rat superior cervical sympathetic ganglion , 1983, Journal of neurocytology.

[33]  J. Altman,et al.  Autoradiographic and histological studies of postnatal neurogenesis. I. A longitudinal investigation of the kinetics, migration and transformation of cells incoorporating tritiated thymidine in neonate rats, with special reference to postnatal neurogenesis in some brain regions , 1966, The Journal of comparative neurology.

[34]  M. Spatz,et al.  Transplacental Chemical Induction of Microencephaly in Two Strains of Rats. I , 1968, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[35]  W. J. Tze,et al.  Adverse effects of maternal alcohol consumption on pregnancy and foetal growth in rats , 1975, Nature.

[36]  J. Coyle,et al.  Histological and neurochemical effects of fetal treatment with methylazoxymethanol on rat neocortex in adulthood , 1979, Brain Research.

[37]  M. Miller,et al.  Effect of prenatal exposure to ethanol on the development of cerebral cortex: I. Neuronal generation. , 1988, Alcoholism, clinical and experimental research.

[38]  M A Warren,et al.  Synapse‐to‐neuron ratios in the visual cortex of adult rats undernourished from about birth until 100 days of age , 1982, The Journal of comparative neurology.