[1]
|
Bâ, A., Seri, B.V., Aka, K.J., Glin, L. and Tako, A. (1999) Comparative Effects of Developmental Thiamine Deficiencies and Ethanol Exposure on the Morphometry of the CA3 Pyramidal Cells. Neurotoxicology and Teratology, 21, 579-586. https://doi.org/10.1016/S0892-0362(99)00014-8
|
[2]
|
Berman, R.F. and Hannigan, J.H. (2000) Effects of Prenatal Alcohol Exposure on the Hippocampus, Spatial Behavior, Electrophysiology, and Neuroanatomy. Hippocampus, 10, 94-110. https://doi.org/10.1002/(SICI)1098-1063(2000)10:1%3C94::AID-HIPO11%3E3.0.CO;2-T
|
[3]
|
Bâ, A. (2011) Comparative Effects of Alcohol and Thiamine Deficiency on the Developing Central Nervous System. Behavioural Brain Research, 225, 235-242. https://doi.org/10.1016/j.bbr.2011.07.015
|
[4]
|
Guerri, C. (2002) Mechanisms Involved in Central Nervous System Dysfunctions Induced by Prenatal Ethanol Exposure. Neurotoxicity Research, 4, 327-335. https://doi.org/10.1080/1029842021000010884
|
[5]
|
Mattson, S.N., Bernes, G.A. and Doyle, L.R. (2019) Fetal Alcohol Spectrum Disorders: A Review of the Neurobehavioral Deficits Associated with Prenatal Alcohol Exposure. Alcoholism: Clinical and Experimental Research, 43, 1046-1062. https://doi.org/10.1111/acer.14040
|
[6]
|
Krulewitch, C.J. (2005) Alcohol Consumption during Pregnancy. Annual Review of Nursing Research, 23, 101-134. https://doi.org/10.1891/0739-6686.23.1.101
|
[7]
|
Guerri, C., Bazinet, A. and Riley, E.P. (2009) Foetal Alcohol Spectrum Disorders and Alterations in Brain and Behaviour. Alcohol and Alcoholism, 44,108-114. https://doi.org/10.1093/alcalc/agn105
|
[8]
|
Ripabelli, G., Cimmino, L. and Grasso, G.M. (2006) Alcohol Consumption, Pregnancy and Fetal Alcohol Syndrome, Implications in Public Health and Preventive Strategies. Annali di Igiene, 18, 391-406.
|
[9]
|
Bakoyiannis, I., Gkioka, E., Pergialiotis, V., Mastroleon, I., Prodromidou, A., Vlachos, G.D. and Perrea, D. (2014) Fetal Alcohol Spectrum Disorders and Cognitive Functions of Young Children. Reviews in the Neurosciences, 25, 631-639. https://doi.org/10.1515/revneuro-2014-0029
|
[10]
|
Dierssen, M. and Ramakers, G.J. (2006) Dendritic Pathology in Mental Retardation, from Molecular Genetics to Neurobiology. Genes, Brain and Behavior, 5, 48-60. https://doi.org/10.1111/j.1601-183X.2006.00224.x
|
[11]
|
Kodituwakku, P.W. (2009) Neurocognitive Profile in Children with Fetal Alcohol Spectrum Disorders. Developmental Disabilities Research Reviews, 15, 218-224. https://doi.org/10.1002/ddrr.73
|
[12]
|
du Plessis, L., Jacobson, S.W., Molteno, C.D., Robertson, F.C., Peterson, B.S., Jacobson, J.L. and Meintjes, E.M. (2014) Neural Correlates of Cerebellar-Mediated Timing during Finger Tapping in Children with Fetal Alcohol Spectrum Disorders. Neuroimage: Clinical, 7, 562-570. https://doi.org/10.1016/j.nicl.2014.12.016
|
[13]
|
Khoury, J.E., Milligan, K. and Girard, T.A. (2015) Executive Functioning in Children and Adolescents Prenatally Exposed to Alcohol: A Meta Analytic Review. Neuropsychology Review, 25, 149-170. https://doi.org/10.1007/s11065-015-9289-6
|
[14]
|
Kingdon D., Cardoso C., McGrath J.J. (2016) Research Review: Executive Function Deficits in Fetal Alcohol Spectrum Disorders and Attention-Deficit/Hyperactivity Disorder—A Meta-Analysis. Journal of Child Psychology and Psychiatry, 57, 116-131. https://doi.org/10.1111/jcpp.12451
|
[15]
|
Mattson, J.T., Thorne, J.C. and Kover, S.T. (2020) Relationship between Task-Based and Parent Report-Based Measures of Attention and Executive Function in Children with Fetal Alcohol Spectrum Disorders (FASD). Journal of Pediatric Neuropsychology, 6, 176-188. https://doi.org/10.1007/s40817-020-00089-0
|
[16]
|
Paolozza, A., Rasmussen, C., Pei, J., Hanlon-Dearman, A., Nikkel, S.M., Andrew, G., et al. (2014) Working Memory and Visuospatial Deficits Correlate with Oculomotor control in Children with Fetal Alcohol Spectrum Disorder. Behavioural Brain Research, 263, 70-79. https://doi.org/10.1016/j.bbr.2014.01.024
|
[17]
|
Lewis, C.E., Thomas, K.G., Dodge, N.C., Molteno, C.D., Meintjes, E.M., Jacobson, J.L. and Jacobson, S.W. (2015) Verbal Learning and Memory Impairment in Children with Fetal Alcohol Spectrum Disorders. Alcoholism: Clinical and Experimental Research, 39, 724-732. https://doi.org/10.1111/acer.12671
|
[18]
|
Marquardt, K. and Brigman, J.L. (2016) The Impact of Prenatal Alcohol Exposure on Social, Cognitive and Affective Behavioral Domains: Insights from Rodent Models. Alcohol, 51, 1-15. https://doi.org/10.1016/j.alcohol.2015.12.002
|
[19]
|
Louw, J.G., van Heerden, A., Olivier, L., Lambrechts, T., Broodryk, M., Bunge L., et al. (2021) Executive Function after Prenatal Alcohol Exposure in Children in a South African Population: Cross-sectional Study. JMIR Formative Research, 5, e20658. https://doi.org/10.2196/20658
|
[20]
|
Moore, E.M., Migliorini, R., Infante, M.A. and Riley, E.P. (2014) Fetal Alcohol Spectrum Disorders, Recent Neuroimaging Findings. Current Developmental Disorders Reports, 1, 161-172. https://doi.org/10.1007/s40474-014-0020-8
|
[21]
|
Bhattacharya D., Dunaway E.P., Bhattacharya S., Bloemer J., Buabeid M., Escobar M., et al. (2015) Impaired ILK Function Is Associated with Deficits in Hippocampal Based Memory and Synaptic Plasticity in a FASD Rat Model. PLoS ONE, 10, e0135700. https://doi.org/10.1371/journal.pone.0135700
|
[22]
|
Avchalumova, Y. and Mandyama, C.D. (2020) Synaptic Plasticity and Its Modulation by Alcohol. Brain Plasticity, 6, 103-111. https://doi.org/10.3233/BPL-190089
|
[23]
|
Autti-Rämö, I., Autti, T., Korkman, M., Kettunen, S., Salonen, O. and Valanne, L. (2002) MRI Findings in Children with School Problems Who Had Been Exposed Prenatally to Alcohol. Developmental Medicine and Child Neurology, 44, 98-106. https://doi.org/10.1017/S0012162201001748
|
[24]
|
Glass, L., Ware, A.L. and Mattson, S.N. (2014) Neurobehavioral, Neurologic, and Neuroimaging Characteristics of Fetal Alcohol Spectrum Disorders. Handbook of Clinical Neurology, 125, 435-462. https://doi.org/10.1016/B978-0-444-62619-6.00025-2
|
[25]
|
Cardenas, V.A., Price, M., Infante, M.A., Moore, E.M., Mattson, S.N., Riley, E.P. and Fein, G. (2014) Automated Cerebellar Segmentation, Validation and Application to Detect Smaller Volumes in Children Prenatally Exposed to Alcohol. Neuroimage: Clinical, 4, 295-301. https://doi.org/10.1016/j.nicl.2014.01.002
|
[26]
|
Donald, K.A., Eastman, E., Howells, F.M., Adnams, C., Riley, E.P., Woods, R.P., et al. (2015) Neuroimaging Effects of Prenatal Alcohol Exposure on the Developing Human Brain: A Magnetic Resonance Imaging Review. Acta Neuropsychiatrica, 27, 251-269. https://doi.org/10.1017/neu.2015.12
|
[27]
|
Sutherland, G.T., Sheahan, P.J., Matthews, J., Dennis, C.V., Sheedy, D.S., McCrossin, T., et al. (2013) The Effects of Chronic Alcoholism on Cell Proliferation in the Human Brain. Experimental Neurology, 247, 9-18. https://doi.org/10.1016/j.expneurol.2013.03.020
|
[28]
|
Rice, J. and Gu, C. (2019) Function and Mechanism of Myelin Regulation in Alcohol Abuse and Alcoholism. Bioessays, 41, e1800255. https://doi.org/10.1002/bies.201800255
|
[29]
|
Chandran, S., Sreeraj, V.S., Venkatasubramanian, G., Sathyaprabha, T.N. and Murthy, P. (2021) Corpus Callosum Morphometry in Children with Prenatal Alcohol Exposure. Psychiatry Research: Neuroimaging, 318, Article ID: 111405. https://doi.org/10.1016/j.pscychresns.2021.111405
|
[30]
|
Bookstein, F.L., Streissguth, A.P., Sampson, P.D., Connor, P.D. and Barr, H.M. (2002) Corpus Callosum Shape and Neuropsychological Deficits in Adult Males with Heavy Fetal Alcohol Exposure. Neuroimage, 15, 233-251. https://doi.org/10.1006/nimg.2001.0977
|
[31]
|
Ba, A., Seri, B.V. and Han, S.H. (1996) Thiamine Administration during Chronic Alcohol Intake in Pregnant and Lactating Rats, Effects on the Offspring Neurobehavioural Development. Alcohol and Alcoholism, 31, 27-40. https://doi.org/10.1093/oxfordjournals.alcalc.a008113
|
[32]
|
Bonthius, D. and West, J.R. (1988) Blood Alcohol Concentration and Microencephaly: A Dose-Response Study in the Neonatal Rat. Teratology, 37, 223-231. https://doi.org/10.1002/tera.1420370307
|
[33]
|
González-Burgos, I., Alejandre-Gómez, M., Olvera-Cortés, M.E., Pérez-Vega, M.I., Evans, S. and Feria-Velasco, A. (2006) Prenatal-Through-Postnatal Exposure to Moderate Levels of Ethanol Leads to Damage on the Hippocampal CA1 Field of Juvenile Rats: A Stereology and Golgi Study. Neuroscience Research, 56, 400-408. https://doi.org/10.1016/j.neures.2006.08.007
|
[34]
|
Bâ, A. (2009) Alcohol and B1 Vitamin Deficiency-Related Stillbirths. The Journal of Maternal-Fetal and Neonatal Medicine, 22, 452-457. https://doi.org/10.1080/14767050802609775
|
[35]
|
Ba, A. (2012) Paradoxical Effects of Alcohol and Thiamine Deficiency on the Eye Opening in Rat Pups. The Journal of Maternal-Fetal and Neonatal Medicine, 25, 2435-2440. https://doi.org/10.3109/14767058.2012.703712
|
[36]
|
Sakata-Haga, H., Sawada, K., Hisano, S. and Fukui, Y. (2001) Abnormalities of Cerebellar Foliation in Rats Prenatally Exposed to Ethanol. Acta Neuropathologica, 102, 36-40. https://doi.org/10.1007/s004010000345
|
[37]
|
Sakata-Haga, H., Sawada, K., Ohnishi, T. and Fukui, Y. (2004) Hydrocephalus Following Prenatal Exposure to Ethanol. Acta Neuropathologica, 108, 393-398. https://doi.org/10.1007/s00401-004-0901-8
|
[38]
|
Fukui, Y. and Sakata-Haga, H. (2009) Intrauterine Environment-Genome Interaction and Children’s Development (1): Ethanol: A Teratogen in Developing Brain. The Journal of Toxicological Sciences, 34, SP273-SP278. https://doi.org/10.2131/jts.34.SP273
|
[39]
|
Marquardt, K. and Brigman, J.L. (2016) The Impact of Prenatal Alcohol Exposure on Social, Cognitive and Affective Behavioral Domains: Insights from Rodent Models. Alcohol, 51, 1-15. https://doi.org/10.1016/j.alcohol.2015.12.002
|
[40]
|
Tang, S., Xu, S., Waddell, J., Zhu, W., Gullapalli, R.P. and Mooney, S.M. (2019) Functional Connectivity and Metabolic Alterations in Medial Prefrontal Cortex in a Rat Model of Fetal Alcohol Spectrum Disorder: A Resting State Functional MRI and in vivo Proton MR Spectroscopy Study. Developmental Neuroscience, 41, 67-78. https://doi.org/10.1159/000499183
|
[41]
|
Sakata-Haga, H., Sawada, K., Ohta, K., Cui, C., Hisano, S. and Fukui, Y. (2003) Adverse Effects of Maternal Ethanol Consumption on Development of Dorsal Hippocampus in Rat Offspring. Acta Neuropathologica, 105, 30-36. https://doi.org/10.1007/s00401-002-0606-9
|
[42]
|
Rice, D. and Barone, S. Jr. (2000) Critical Periods of Vulnerability for the Developing Nervous System: Evidence from Humans and Animal Models. Environ Health Perspectives, 108, 511-533. https://doi.org/10.1289/ehp.00108s3511
|
[43]
|
Riar, A.K., Narasimhan, M., Rathinam, M.L., Henderson, G.I. and Mahimainatha, L. (2016) Ethanol Induces Cytostasis of Cortical Basal Progenitors. Journal of Biomedical Science, 23, 1-13. https://doi.org/10.1186/s12929-016-0225-8
|
[44]
|
Miller, M.W. (1988) Effect of Prenatal Exposure to Ethanol on the Development of Cerebral Cortex: I. Neuronal Generation. Alcoholism: Clinical and Experimental Research, 12, 440-449. https://doi.org/10.1111/j.1530-0277.1988.tb00223.x
|
[45]
|
Louth, E.L., Bignell, W., Taylor, C.L. and Bailey, C.D. (2016) Developmental Ethanol Exposure Leads to Long-Term Deficits in Attention and Its Underlying Prefrontal Circuitry. eNeuro, 3, 1-21. https://doi.org/10.1523/ENEURO.0267-16.2016
|
[46]
|
Takahashi, T., Nowakowski, R.S. and Caviness, V.S.Jr. (1995) The Cell Cycle of the Pseudostratified Ventricular Epithelium of the Embryonic Murine Cerebral Wall. Journal of Neuroscience, 15, 6046-6057. https://doi.org/10.1523/JNEUROSCI.15-09-06046.1995
|
[47]
|
Sudheendran, N., Bake, S., Miranda, R.C. and Larin, K.V. (2013) Comparative Assessments of the Effects of Alcohol Exposure on Fetal Brain Development Using Optical Coherence Tomography and Ultrasound Imaging. Journal of Biomedical Optics, 18, Article ID: 020506. https://doi.org/10.1117/1.JBO.18.2.020506
|
[48]
|
Santillano, D.R., Kumar, L.S., Prock, T.L., Camarillo, C., Tingling, J.D. and Miranda, R.C. (2005) Ethanol Induces Cell-Cycle Activity and Reduces Stem Cell Diversity to Alter Both Regenerative Capacity and Differentiation Potential of Cerebral cortical Neuroepithelial Precursors. BMC Neuroscience, 6, Article No. 59. https://doi.org/10.1186/1471-2202-6-59
|
[49]
|
Salem, N.A., Mahnke, A.H., Konganti, K., Hillhouse, A.E. and Miranda, R.C. (2021) Cell-Type and Fetal-Sex-Specific Targets of prenatal Alcohol Exposure in Developing Mouse Cerebral Cortex. iScience, 24, Article ID: 102439. https://doi.org/10.1016/j.isci.2021.102439
|
[50]
|
Vemuri, M.C., Chetty, C.S. (2005) Alcohol Impairs Astrogliogenesis by Stem Cells in Rodent Neurospheres. Neurochemistry International, 47, 129-135. https://doi.org/10.1016/j.neuint.2005.04.019
|
[51]
|
Rubert, G., Miñana, R., Pascual, M. and Guerri, C. (2006) Ethanol Exposure during Embryogenesis Decreases the Radial Glial Progenitor Pool and Affects the Generation of Neurons and Astrocytes. Journal of Neuroscience Research, 84, 483-496. https://doi.org/10.1002/jnr.20963
|
[52]
|
Robertson, F.C., Narr, K.L., Molteno, C.D., Jacobson, J.L., Jacobson, S.W. and Meintjes, E.M. (2016) Prenatal Alcohol Exposure Is Associated with Regionally Thinner Cortex during the Preadolescent Period. Cerebral Cortex, 26, 3083-3095. https://doi.org/10.1093/cercor/bhv131
|
[53]
|
O’Rourke, N.A., Dailey, M.E., Smith, S.J. and McConnell, S.K. (1992) Diverse Migratory Pathways in the Developing Cerebral Cortex. Science, 258, 299-302. https://doi.org/10.1126/science.1411527
|
[54]
|
Almeida, L., Andreu-Fernández, V., Navarro-Tapia, E., Aras-López, R., Serra-Delgado, M., Martínez, L., et al. (2020) Murine Models for the Study of Fetal Alcohol Spectrum Disorders: An Overview. Frontiers in Pediatrics, 8, Article 359. https://doi.org/10.3389/fped.2020.00359
|
[55]
|
Delatour, L.C., Yeh, P.W.L. and Yeh, H.H. (2020) Prenatal Exposure to Ethanol Alters Synaptic Activity in Layer V/VI Pyramidal Neurons of the Somatosensory Cortex. Cerebral Cortex, 30, 1735-1751. https://doi.org/10.1093/cercor/bhz199
|
[56]
|
Miller, M.W. (1993) Migration of Cortical Neurons Is Altered by Gestational Exposure to Ethanol. Alcoholism: Clinical and Experimental Research, 17, 304-314. https://doi.org/10.1111/j.1530-0277.1993.tb00768.x
|
[57]
|
Miller, M.W. (1986) Effects of Alcohol on the Generation and Migration of Cerebral Cortical Neurons. Science, 233, 1308-1311. https://doi.org/10.1126/science.3749878
|
[58]
|
Shenoda, B.B. (2017) An Overview of the Mechanisms of Abnormal GABAergic Interneuronal Cortical Migration Associated with Prenatal Ethanol Exposure. Neurochemical Research, 42, 1279-1287. https://doi.org/10.1007/s11064-016-2169-5
|
[59]
|
Xu, G., Broadbelt, K.G., Haynes, R.L., Folkerth, R.D., Borenstein, N.S., Belliveau, R.A., et al. (2011) Late Development of the GABAergic System in the Human Cerebral Cortex and White Matter. Journal of Neuropathology and Experimental Neurology, 70, 841-858. https://doi.org/10.1097/NEN.0b013e31822f471c
|
[60]
|
Smith, S.M., Garic, A., Flentke, G.R. and Berres, E.M. (2014) Neural Crest Development in Fetal Alcohol Syndrome. Birth Defects Research Part C-Embryo Today: Reviews, 102, 210-220. https://doi.org/10.1002/bdrc.21078
|
[61]
|
Dou, X., Menkari, C., Mitsuyama, R., Foroud, T., Wetherill, L., Hammond, P., et al. (2018) L1 Coupling to Ankyrin and the Spectrin-Actin Cytoskeleton Modulates Ethanol Inhibition of L1 Adhesion and Ethanol Teratogenesis. FASEB Journal, 32, 1364-1374. https://doi.org/10.1096/fj.201700970
|
[62]
|
Taléns-Visconti, R., Sanchez-Vera, I., Kostic, J., Perez-Arago, M.A., Erceg, S., Stojkovic, M. and Guerri, C. (2011) Neural Differentiation from Human Embryonic Stem Cells as a Tool to Study Early Brain Development and the Neuroteratogenic Effects of Ethanol. Stem Cells and Development, 20, 327-339. https://doi.org/10.1089/scd.2010.0037
|
[63]
|
Krishnamoorthy, M., Gerwe, B.A., Scharer, C.D., Sahasranaman, V., Eilertson, C.D., Nash, R.J., et al. (2013) Ethanol Alters Proliferation and Differentiation of Normal and Chromosomally Abnormal Human Embryonic Stem Cell-Derived Neurospheres. Birth Defects Research Part B: Developmental and Reproductive Toxicology, 98, 283-295. https://doi.org/10.1002/bdrb.21063
|
[64]
|
Camarillo, C. and Miranda, R.C. (2008) Ethanol Exposure during Neurogenesis Induces Persistent Effects on Neural Maturation: Evidence from an ex vivo Model of Fetal Cerebral Cortical Neuroepithelial Progenitor Maturation. Gene Expression, 14, 159-171.
|
[65]
|
Serio, R.N., Laursen, K.B., Urvalek, A.M., Gross, S.S. and Gudas, L.J. (2019) Ethanol Promotes Differentiation of Embryonic Stem Cells through Retinoic Acid Receptor-γ. Journal of Biological Chemistry, 294, 5536-5548. https://doi.org/10.1074/jbc.RA118.007153
|
[66]
|
Zhou, F.C., Balaraman, Y., Teng, M., Liu, Y., Singh, R.P. and Nephew, K.P. (2011) Alcohol Alters DNA Methylation Patterns and Inhibits Neural Stem Cell Differentiation. Alcoholism: Clinical and Experimental Research, 35, 735-746. https://doi.org/10.1111/j.1530-0277.2010.01391.x
|
[67]
|
Liu, Y., Balaraman, Y., Wang, G., Nephew, K.P. and Zhou, F.C. (2009) Alcohol Exposure Alters DNA Methylation Profilesin Mouse Embryos at Early Neurulation. Epigenetics, 4, 500-511. https://doi.org/10.4161/epi.4.7.9925
|
[68]
|
Mandal, C., Halder, D., Jung, K.H. and Chai, Y.G. (2017) Gestational Alcohol Exposure Altered DNA Methylation Status in the Developing Fetus. International Journal of Molecular Sciences, 18, Article 1386. https://doi.org/10.3390/ijms18071386
|
[69]
|
Serio, R.N. and Gudas, L.J. (2020) Modification of Stem Cell States by Alcohol and Acetaldehyde. Chemico-Biological Interactions, 316, Article ID: 108919. https://doi.org/10.1016/j.cbi.2019.108919
|
[70]
|
Bonthius, D.J. and West, J.R. (1991) Permanent Neuronal Deficits in Rats Exposed to Alcohol during the Brain Growth Spurt. Teratology, 44, 147-163. https://doi.org/10.1002/tera.1420440203
|
[71]
|
Ba, A. (2017) Alcohol and Thiamine Deficiency Trigger Differential Mitochondrial Transition Pore Opening Mediating Cellular Death. Apoptosis, 22, 741-752. https://doi.org/10.1007/s10495-017-1372-4
|
[72]
|
Ikonomidou, C., Bittigau, P., Ishimaru, M.J., Wozniak, D.F., Koch, C., Genz, K., et al. (2000) Ethanol-Induced Apoptotic Neurodegeneration and Fetal Alcohol Syndrome. Science, 287, 1056-1060. https://doi.org/10.1126/science.287.5455.1056
|
[73]
|
Lamarche, F., Carcenac, C., Gonthier, B., Cottet-Rousselle, C., Chauvin, C., Barret, L., et al. (2013) Mitochondrial Permeability Transition Pore Inhibitors Prevent Ethanol-Induced Neuronal Death in Mice. Chemical Research in Toxicology, 26, 78-88. https://doi.org/10.1021/tx300395w
|
[74]
|
Livy, D.J., Miller, E.K., Maier, S.E. and West, J.R. (2003) Fetal Alcohol Exposure and Temporal Vulnerability Effects of Binge-Like Alcohol Exposure on the Developing Rat Hippocampus. Neurotoxicology and Teratology, 25, 447-458. https://doi.org/10.1016/S0892-0362(03)00030-8
|
[75]
|
Miki, T., Harris, S.J., Wilce, P.A., Takeuchi, Y. and Bedi, K.S. (2004) Effects of Age and Alcohol Exposure during Early Life on Pyramidal Cell Numbers in the CA1-CA3 Region of the Rat Hippocampus. Hippocampus, 14, 124-134. https://doi.org/10.1002/hipo.10155
|
[76]
|
Smith, C.C., Guévremont, D., Williams, J.M. and Napper, R.M. (2015) Apoptotic Cell Death and Temporal Expression of Apoptotic Proteins Bcl-2 and Bax in the Hippocampus, following Binge Ethanol in the Neonatal Rat Model. Alcoholism: Clinical and Experimental Research, 39, 36-44. https://doi.org/10.1111/acer.12606
|
[77]
|
Maier, S.E. and West, J.R. (2001) Regional Differences in Cell Loss Associated with Binge-Like Alcohol Exposure during the First Two Trimesters Equivalent in the Rat. Alcohol, 23, 49-57. https://doi.org/10.1016/S0741-8329(00)00133-6
|
[78]
|
Dikranian, K., Qin, Y.-Q., Labruyere, J., Nemmers, B. and Olney, J.W. (2005) Ethanol-Induced Neuroapoptosis in the Developing Rodent Cerebellum and Related Brain Stem Structures. Brain Research. Developmental Brain Research, 155, 1-13. https://doi.org/10.1016/j.devbrainres.2004.11.005
|
[79]
|
Wozniak, D.F., Hartman, R.E., Boyle, M.P., Vogt, S.K., Brooks, A.R., Tenkova, T., et al. (2004) Apoptotic Neurodegeneration Induced by Ethanol in Neonatal Mice Is Associated with Profound Learning/Memory Deficits in Juveniles followed by Progressive Functional Recovery in Adults. Neurobiology of Disease, 17, 403-414. https://doi.org/10.1016/j.nbd.2004.08.006
|
[80]
|
Bukiya, A.N. (2019) Fetal Cerebral Artery Mitochondrion as Target of Prenatal Alcohol Exposure. International Journal of Environmental Research and Public Health, 16, Article 1586. https://doi.org/10.3390/ijerph16091586
|
[81]
|
Park, Y.H., Jeong, M.S. and Jang, S.B. (2014) Death Domain Complex of the TNFR-1, TRADD, and RIP1 Proteins for Death-Inducing Signaling. Biochemical and Biophysical Research Communications, 443, 1155-1161. https://doi.org/10.1016/j.bbrc.2013.12.068
|
[82]
|
Chu, J., Tong, M. and de la Monte, S.M. (2007) Chronic Ethanol Exposure Causes Mitochondrial Dysfunction and Oxidative Stress in Immature Central Nervous System Neurons. Acta Neuropathologica, 113, 659-673. https://doi.org/10.1007/s00401-007-0199-4
|
[83]
|
Gibson, G.E. and Blass, J.P. (2007) Thiamine-Dependent Processes and Treatment Strategies in Neurodegeneration. Antioxidants & Redox Signaling, 9, 1605-1619. https://doi.org/10.1089/ars.2007.1766
|
[84]
|
Ba, A., N’Douba, V., d’Almeida, M.A. and Seri B.V. (2005) Effects of Maternal Thiamine Deficiencies on the Pyramidal and Granule Cells of the Hippocampus of Rat Pups. Acta Neurobiologiae Experimentalis, 65, 387-398.
|
[85]
|
Schwarz, M., Andrade-Navarro, M.A. and Gross, A. (2007) Mitochondrial Carriers and Pores: Key Regulators of the Mitochondrial Apoptotic Program? Apoptosis, 12, 869-876. https://doi.org/10.1007/s10495-007-0748-2
|
[86]
|
Wensveen, F.M., Alves, N.L., Derks, I.A.M., Reedquist, K.A. and Eldering, E. (2011) Apoptosis Induced by Overall Metabolic Stress Converges on the Bcl-2 Family Proteins Noxa and Mcl-1. Apoptosis, 16, 708-721. https://doi.org/10.1007/s10495-011-0599-8
|
[87]
|
Ba, A. (2008) Metabolic and Structural Role of Thiamine in Nervous Tissues. Cellular and Molecular Neurobiology, 28, 923-931. https://doi.org/10.1007/s10571-008-9297-7
|
[88]
|
Reitz, R.C. (1993) Dietary Fatty Acids and Alcohol: Effects on Cellular Membranes. Alcohol and Alcoholism, 28, 59-71.
|
[89]
|
Montoliu, C., Vallés, S., Renau-Piqueras, J. and Guerri, C. (1994) Ethanol-Induced Oxygen Radical Formation and Lipid Peroxidation in Rat Brain: Effect of Chronic Alcohol Consumption. Journal of Neurochemistry, 63, 1855-1862. https://doi.org/10.1046/j.1471-4159.1994.63051855.x
|
[90]
|
Barry, J. A. and Gawrisch, K. (1994) Direct NMR Evidence for Ethanol Binding to the Lipid-Water Interface of Phospholipid Bilayers. Biochemistry, 33, 8082-8088. https://doi.org/10.1021/bi00192a013
|
[91]
|
Dianzani, M.U. (1985) Lipid Peroxidation in Ethanol Poisoning: A Critical Reconsideration. Alcohol and Alcoholism, 20, 161-173.
|
[92]
|
Granato, A. and Dering, B. (2018) Alcohol and the Developing Brain: Why Neurons die and How Survivors Change. International Journal of Molecular Science, 19, Article 2992. https://doi.org/10.3390/ijms19102992
|
[93]
|
Olney, J.W. (2014) Focus on Apoptosis to Decipher How Alcohol and Many Other Drugs Disrupt Brain Development. Frontiers in Pediatrics, 2, Article 81. https://doi.org/10.3389/fped.2014.00081
|
[94]
|
Tessier-Lavigne, M., Placzek, M., Lumsden, A.G.S., Dodd, J. and Jessell, T.M. (1988) Chemotropic Guidance of Developing Axons in the Mammalian Central Nervous System. Nature, 336, 775-778. https://doi.org/10.1038/336775a0
|
[95]
|
Ye, X., Qiu, Y., Gao, Y., Wan, D. and Zhu, H. (2019) A Subtle Network Mediating Axon Guidance: Intrinsic Dynamic Structure of Growth Cone, Attractive and Repulsive Molecular Cues, and the Intermediate Role of Signaling Pathways. Neural Plasticity, 2019, Article ID: 1719829. https://doi.org/10.1155/2019/1719829
|
[96]
|
Kiss, A., Fischer, I., Kleele, T., Misgeld, T. and Propst, F. (2018) Neuronal Growth Cone Size-Dependent and -Independent Parameters of Microtubule Polymerization. Frontiers in Cellular Neuroscience, 12, Article 195. https://doi.org/10.3389/fncel.2018.00195
|
[97]
|
Granato, A., Di Rocco, F., Zumbo, A., Toesca, A. and Giannetti, S. (2003) Organization of Cortico-Cortical Associative Projections in Rats Exposed to Ethanol during Early Postnatal Life. Brain Research Bulletin, 60, 339-344. https://doi.org/10.1016/S0361-9230(03)00052-2
|
[98]
|
Granato, A., Santarelli, M., Sbriccoli, A. and Minciacchi, D. (1995) Multifaceted Alterations of the Thalamo-Cortico-Thalamic Loop in Adult Rats Prenatally Exposed to Ethanol. Anatomy and Embryology (Berlin), 191, 11-23. https://doi.org/10.1007/BF00215293
|
[99]
|
Minciacchi, D., Granato, A., Santarelli, M. and Sbriccoli, A. (1993) Modifications of Thalamo-Cortical Circuitry in Rats Prenatally Exposed to Ethanol. Neuroreport, 4, 415-418. https://doi.org/10.1097/00001756-199304000-00019
|
[100]
|
Xie, N., Yang, Q., Chappell, T.D., Li, C.X. and Waters, R.S. (2010) Prenatal Alcohol Exposure Reduces the Size of the Forelimb Representation in Motor Cortex in Rat: An Intracortical Microstimulation (ICMS) Mapping Study. Alcohol, 44, 185-194. https://doi.org/10.1016/j.alcohol.2009.10.014
|
[101]
|
Ye, X., Qiu, Y., Gao, Y., Wan, D. and Zhu, H. (2019) A Subtle Network Mediating Axon Guidance: Intrinsic Dynamic Structure of Growth Cone, Attractive and Repulsive Molecular Cues, and the Intermediate Role of Signaling Pathways. Neural Plasticity, 2019, Article ID: 1719829. https://doi.org/10.1155/2019/1719829
|
[102]
|
Piper, M., Plachez, C., Zalucki, O., Fothergill, T., Goudreau, G., Erzurumlu, R., Gu, C. and Richards, L.J. (2009) Neuropilin 1-Sema Signaling Regulates Crossing of Cingulate Pioneering Axons during Development of the Corpus Callosum. Cerebral Cortex, 19, i11-i21. https://doi.org/10.1093/cercor/bhp027
|
[103]
|
Mathews, E., Dewees, K., Diaz, D. and Favero, C. (2021) White Matter Abnormalities in Fetal Alcohol Spectrum Disorders: Focus on Axon Growth and Guidance. Experimental Biology and Medicine, 246, 812-821. https://doi.org/10.1177/1535370220980398
|
[104]
|
Sepulveda, B., Carcea, I., Zhao, B., Salton, S.R. and Benson, D.L. (2011) L1 Cell Adhesion Molecule Promotes Resistance to Alcohol-Induced Silencing of Growth Cone Responses to Guidance Cues. Neuroscience, 180, 30-40. https://doi.org/10.1016/j.neuroscience.2011.02.018
|
[105]
|
Mrak, R.E. (1992) Opposite Effects of Dimethyl Sulfoxide and Ethanol on Synaptic Membrane Fluidity. Alcohol, 9, 513-517. https://doi.org/10.1016/0741-8329(92)90089-S
|
[106]
|
Hanchar, H.J., Chutsrinopkun, P., Meera, P., Supavilai, P., Sieghart, W., Wallner, M. and Olsen, R.W. (2006) Ethanol Potently and Competitively Inhibits Binding of the Alcohol Antagonist Ro15-4513 to alpha4/6beta3delta GABAA Receptors. Proceedings of National Academy of Sciences, USA, 103, 8546-8551. https://doi.org/10.1073/pnas.0509903103
|
[107]
|
Arevalo, E., Shanmugasundararaj, S., Wilkemeyer, M.F., Dou, X., Chen, S., Charness, M.E. and Miller, K.W. (2008) An Alcohol Binding Site on the Neural Cell Adhesion Molecule L1. Proceedings of National Academy of Sciences of the United States of America, 105, 371-375. https://doi.org/10.1073/pnas.0707815105
|
[108]
|
Tang, N., Farah, B., He, M., Fox, S., Malouf, A., Littner, Y. and Bearer, C.F. (2011) Ethanol Causes the Redistribution of L1 Cell Adhesion Molecule in Lipid Rafts. Journal of Neurochemistry, 119, 859-867. https://doi.org/10.1111/j.1471-4159.2011.07467.x
|
[109]
|
Littner, Y., Tang, N., He, M. and Bearer, C.F. (2013) L1 Cell Adhesion Molecule Signaling Is Inhibited by Ethanol in vivo. Alcoholism: Clinical and Experimental Research, 37, 383-389. https://doi.org/10.1111/j.1530-0277.2012.01944.x
|
[110]
|
Huntley, G.W. and Benson, D.L. (1999) Neural (N)-Cadherin at Developing Thalamo-cortical Synapses Provides an Adhesion Mechanism for the Formation of Somatopically Organized Connections. Journal of Comparative Neurology, 407, 453-471. https://doi.org/10.1002/(SICI)1096-9861(19990517)407:4%3C453::AID-CNE1%3E3.0.CO;2-4
|
[111]
|
Mintz, C.D., Dickson, T.C., Gripp, M.L., Salton, S.R. and Benson, D.L. (2003) ERMs Colocalize Transiently with L1 during Neocortical Axon Outgrowth. Journal of Comparative Neurology, 464, 438-448. https://doi.org/10.1002/cne.10809
|
[112]
|
Lagenaur, C. and Lemmon, V. (1987) An L1-Like Molecule, the 8D9 Antigen, Is a Potent Substrate for Neurite Extension. Proceedings of National Academy of Sciences of the United States of America, 84, 7753-7757. https://doi.org/10.1073/pnas.84.21.7753
|
[113]
|
Stallcup, W.B. and Beasley, L. (1985) Involvement of the Nerve Growth Factor-Inducible Large External Glycoprotein (NILE) in Neurite Fasciculation in Primary Cultures of Rat Brain. Proceedings of National Academy of Sciences of the United States of America, 82, 1276-1280. https://doi.org/10.1073/pnas.82.4.1276
|
[114]
|
Cheng, L. and Lemmon, V. (2004) Pathological Missense Mutations of Neural Cell Adhesion Molecule L1 Affect Neurite Outgrowth and Branching on an L1 Substrate. Molecular and Cellular Neuroscience, 27, 522-530. https://doi.org/10.1016/j.mcn.2004.08.005
|
[115]
|
Castellani, V., De Angelis, E., Kenwrick, S. and Rougon, G. (2002) Cis and Trans Interactions of L1 with Neuropilin-1 Control Axonal Responses to Semaphorin 3A. The EMBO Journal, 21, 6348-6357. https://doi.org/10.1093/emboj/cdf645
|
[116]
|
Haspel, J. and Grumet, M. (2003) The L1CAM Extracellular Region, a Multi-Domain Protein with Modular and Cooperative Binding Modes. Frontiers in Bioscience, 8, s1210-s1225. https://doi.org/10.2741/1108
|
[117]
|
Schaefer, A.W., Kamiguchi, H., Wong, E.V., Beach, C.M., Landreth, G. and Lemmon, V. (1999) Activation of the MAPK Signal Cascade by the Neural Cell Adhesion Molecule L1 Requires L1 Internalization. The Journal of Biological Chemistry, 274, 37965-37973. https://doi.org/10.1074/jbc.274.53.37965
|
[118]
|
Schmid, R.S., Pruitt, W.M. and Maness, P.F. (2000) A MAP Kinase-Signaling Pathway Mediates Neurite Outgrowth on L1 and Requires Src-Dependent Endocytosis. The Journal of Neuroscience, 20, 4177-4188. https://doi.org/10.1523/JNEUROSCI.20-11-04177.2000
|
[119]
|
Dickson, T.C., Mintz, C.D., Benson, D.L. and Salton, S.R. (2002) Functional Binding Interaction Identified between the Axonal CAM L1 and Members of the ERM Family. The Journal of Cell Biology, 157, 1105-1112. https://doi.org/10.1083/jcb.200111076
|
[120]
|
Watanabe, H., Ymazaki, M., Miyazaki, H., Arikawa, C., Itoh, K., Sasaki, T., et al. (2004) Phospholipase D2 Functions as a Downstream Signaling Molecule of MAP kinase Pathway in L1-Stimulated Neurite Outgrowth of Cerebellar Granule Neurons. Journal of Neurochemistry, 89, 142-151. https://doi.org/10.1111/j.1471-4159.2004.02308.x
|
[121]
|
Kamiguchi, H. and Lemmon, V. (2000) Recycling of the Cell Adhesion Molecule L1 in Axonal Growth Cones. The Journal of Neuroscience, 20, 3676-3686. https://doi.org/10.1523/JNEUROSCI.20-10-03676.2000
|
[122]
|
Wong, E.V., Kenwrick, S., Willems, P. and Lemmon, V. (1995) Mutations in the Cell Adhesion Molecule L1 Cause Mental Retardation. Trends in Neurosciences, 18, 168-172. https://doi.org/10.1016/0166-2236(95)93896-6
|
[123]
|
Kenwrick, S., Watkins, A. and De Angelis, E. (2000) Neural Cell Recognition Molecule L1: Relating Biological Complexity to Human Disease Mutations. Human Molecular Genetics, 9, 879-886. https://doi.org/10.1093/hmg/9.6.879
|
[124]
|
Ramanathan, R., Wilkemeyer, M.F., Mittal, B., Perides, G. and Charness, M.E. (1996) Alcohol Inhibits Cell-Cell Adhesion Mediated by Human L1. The Journal of Cell Biology, 133, 381-390. https://doi.org/10.1083/jcb.133.2.381
|
[125]
|
Bearer, C.F., Swick, A.R., O'Riordan, M.A. and Cheng, G. (1999) Ethanol Inhibits L1-Mediated Neurite Outgrowth in Postnatal Rat Cerebellar Granule Cells. The Journal of Biological Chemistry, 274, 13264-13270. https://doi.org/10.1074/jbc.274.19.13264
|
[126]
|
Tang, N., He, M., O'Riordan, M.A., Farkas, C., Buck, K., Lemmon, V. and Bearer, C.F. (2006) Ethanol Inhibits L1 Cell Adhesion Molecule Activation of Mitogen-Activated Protein Kinases. Journal of Neurochemistry, 96, 1480-1490. https://doi.org/10.1111/j.1471-4159.2006.03649.x
|
[127]
|
Charness, M.E., Safran, R.M. and Perides, G. (1994) Ethanol Inhibits Neural Cell-Cell Adhesion. The Journal of Biological Chemistry, 269, 9304-9309. https://doi.org/10.1016/S0021-9258(17)37108-9
|
[128]
|
Vallejo, Y., Hortsch, M. and Dubreuil, R.R. (1997) Ethanol Does Not Inhibit the Adhesive Activity of Drosophila Neuroglian or Human L1 in Drosophila S2 Tissue Culture Cells. The Journal of Biological Chemistry, 272, 12244-12247. https://doi.org/10.1074/jbc.272.18.12244
|
[129]
|
Hoffman, E.J., Mintz, C.D., Wang, S., McNickle, D.G., Salton, S.R.J. and Benson, D.L. (2008) Effects of Ethanol on Axon Outgrowth and Branching in Developing Rat Cortical Neurons. Neuroscience, 157, 556-565. https://doi.org/10.1016/j.neuroscience.2008.08.071
|
[130]
|
Yeaney, N.K., He, M., Tang, N., Malouf, A.T., O'Riordan, M.A., Lemmon, V., and Bearer C.F. (2009) Ethanol Inhibits L1 Cell Adhesion Molecule Tyrosine Phosphorylation and Dephosphorylation and Activation of pp60(src). Journal of Neurochemistry, 110, 779-790. https://doi.org/10.1111/j.1471-4159.2009.06143.x
|
[131]
|
Wilkemeyer, M.F., Menkari, C.E. and Charness, M.E. (2002) Novel Antagonists of Alcohol Inhibition of L1-Mediated Cell Adhesion, Multiple Mechanisms of Action. Molecular Pharmacology, 62, 1053-1060. https://doi.org/10.1124/mol.62.5.1053
|
[132]
|
Dou, X., Menkari, C.E., Shanmugasundararaj, S., Miller, K.W. and Charness, M.E. (2011) Two Alcohol Binding Residues Interact across a Domain Interface of the L1 Neural Cell Adhesion Molecule and Regulate Cell Adhesion. The Journal of Biological Chemistry, 286, 16131-16139. https://doi.org/10.1074/jbc.M110.209254
|
[133]
|
Kaufmann, W.E. and Moser, H.W. (2000) Dendritic Anomalies in Disorders Associated with Mental Retardation. Cerebral Cortex, 10, 981-991. https://doi.org/10.1093/cercor/10.10.981
|
[134]
|
London, M. and Häusser, M. (2005) Dendritic Computation. Annual Review of Neuroscience, 28, 503-532. https://doi.org/10.1146/annurev.neuro.28.061604.135703
|
[135]
|
Armstrong, D.D., Dunn, K. and Antalffy, B. (1998) Decreased Dendritic Branching in Frontal, Motor and Limbic Cortex in Rett Syndrome Compared with Trisomy 21. Journal of Neuropathology and Experimental Neurology, 57, 1013-1017. https://doi.org/10.1097/00005072-199811000-00003
|
[136]
|
Romero, A.M., Renau-Piqueras, J., Marin, M.P., Timoneda, J., Berciano, M.T., Lafarga, M. and Esteban-Pretel, G. (2013) Chronic Alcohol Alters Dendritic Spine Development in Neurons in Primary Culture. Neurotoxicity Research, 24, 532-548. https://doi.org/10.1007/s12640-013-9409-0
|
[137]
|
Purpura, D.P. (1974) Dendritic Spine “Dysgenesis” and Mental Retardation. Science, 186, 1126-1128. https://doi.org/10.1126/science.186.4169.1126
|
[138]
|
Harris, K.M. (1999) Structure, Development, and Plasticity of Dendritic Spines. Current Opinion in Neurobiology, 9, 343-348. https://doi.org/10.1016/S0959-4388(99)80050-6
|
[139]
|
Tarelo-Acuña, L., Olvera-Cortés, E. and González-Burgos, I. (2000) Prenatal and Postnatal Exposure to Ethanol Induces Changes in the Shape of the Dendritic Spines from Hippocampal CA1 Pyramidal Neurons of the Rat. Neuroscience Letters, 286, 13-16. https://doi.org/10.1016/S0304-3940(00)01075-2
|
[140]
|
Stoltenburg-Didinger, G. and Spohr, H. L. (1983) Fetal Alcohol Syndrome and Mental Retardation, Spine Distribution of Pyramidal Cells in Prenatal Alcohol-Exposed Rat Cerebral Cortex; a Golgi Study. Brain Research, 313, 119-123.
|
[141]
|
Hamilton, G.F., Whitcher, L.T. and Klintsova, A.Y. (2010) Postnatal Binge-Like Alcohol Exposure Decreases Dendritic Complexity While Increasing the Density of Mature Spines in mPFC Layer II/III Pyramidal Neurons. Synapse, 64, 127-135. https://doi.org/10.1002/syn.20711
|
[142]
|
Whitcher, L. and Klintsova, A. (2008) Postnatal Binge-Like Alcohol Exposure Reduces Spine Density without Affecting Dendritic Morphology in Rat mPFC. Synapse, 62, 566-573. https://doi.org/10.1002/syn.20532
|
[143]
|
Cui, Z.J., Zhao, K.B., Zhao, H.J., Yu, D.M., Niu, Y.L., Zhang, J.S. and Deng, J.B. (2010) Prenatal Alcohol Exposure Induces Long-Term Changes in Dendritic Spines and Synapses in the Mouse Visual Cortex. Alcohol and Alcoholism, 45, 312-319. https://doi.org/10.1093/alcalc/agq036
|
[144]
|
Yanni, P.A. and Lindsley, T.A. (2000) Ethanol Inhibits Development of Dendrites and Synapses in Rat Hippocampal Pyramidal Neuron Cultures. Brain Research. Developmental Brain Research, 120, 233-243. https://doi.org/10.1016/S0165-3806(00)00015-8
|
[145]
|
Granato, A. and Van Pelt, J. (2003) Effects of Early Ethanol Exposure on Dendrite Growth of Cortical Pyramidal Neurons, Inferences from a Computational Model. Brain Research. Developmental Brain Research, 142, 223-227. https://doi.org/10.1016/S0165-3806(03)00094-4
|
[146]
|
Korkotian, E., Botalova, A., Odegova, T. and Segal, M. (2015) Chronic Exposure to Alcohol Alters Network Activity and Morphology of Cultured Hippocampal Neurons. Neurotoxicology, 47, 62-71. https://doi.org/10.1016/j.neuro.2015.01.005
|
[147]
|
Granato, A., Palmer, L.M., De Giorgio, A., Tavian, D. and Larkum, M.E. (2012) Early Exposure to Alcohol Leads to Permanent Impairment of Dendritic Excitability in Neocortical Pyramidal Neurons. The Journal of Neuroscience, 32, 1377-1382. https://doi.org/10.1523/JNEUROSCI.5520-11.2012
|
[148]
|
Romero, A.M., Esteban-Pretel, G., Marín, M.P., Ponsoda, X., Ballestín, R., Canales, J.J. and Renau-Piqueras, J. (2010) Chronic Ethanol Exposure Alters the Levels, Assembly, and Cellular Organization of the Actin Cytoskeleton and Microtubules in Hippocampal Neurons in Primary Culture. Toxicological Sciences, 118, 602-612. https://doi.org/10.1093/toxsci/kfq260
|
[149]
|
He, J., Nixon, K., Shetty, A.K. and Crews, F.T. (2005) Chronic Alcohol Exposure Reduces Hippocampal Neurogenesis and Dendritic Growth of Newborn Neurons. European Journal of Neuroscience, 21, 2711-2720. https://doi.org/10.1111/j.1460-9568.2005.04120.x
|
[150]
|
Cherra III, S.J. and Jin, Y. (2015) Advances in Synapse Formation, Forging Connections in the Worm. WIREs Developmental Biology, 4, 85-97. https://doi.org/10.1002/wdev.165
|
[151]
|
Harris, K.M. (2020) Structural LTP: From Synaptogenesis to Regulated Synapse Enlargement and Clustering. Current Opinion in Neurobiology, 63, 189-197. https://doi.org/10.1016/j.conb.2020.04.009
|
[152]
|
Fossati, G., Matteoli, M. and Menna, E. (2020) Astrocytic Factors Controlling Synaptogenesis: A Team Play. Cells, 9, Article 2173. https://doi.org/10.3390/cells9102173
|
[153]
|
Martin, S.J., Grimwood, P.D. and Morris, R.G.M. (2000) Synaptic Plasticity and Memory: An Evaluation of the Hypothesis. Annual Review of Neuroscience, 23, 649-711. https://doi.org/10.1146/annurev.neuro.23.1.649
|
[154]
|
Volk, B. (1984) Cerebellar Histogenesis and Synaptic Maturation following Pre- and Postnatal Alcohol Administration. An Electron-Microscopic Investigation of the Rat Cerebellar Cortex. Acta Neuropathologica, 63, 57-65. https://doi.org/10.1007/BF00688471
|
[155]
|
Kyzar, E.J., Floreani, C., Teppen, T.L. and Pandey, S.C. (2016) Adolescent Alcohol Exposure: Burden of Epigenetic Reprogramming, Synaptic Remodeling, and Adult Psychopathology. Frontiers in Neuroscience, 10, Article 222. https://doi.org/10.3389/fnins.2016.00222
|
[156]
|
Lovinger, D.M. and Abrahao, K.P. (2018) Synaptic Plasticity Mechanisms Common to Learning and Alcohol Use Disorder. Learning and Memory, 25, 425-434. https://doi.org/10.1101/lm.046722.117
|
[157]
|
Barnes, J.R., Mukherjee, B., Rogers, B.C., Nafar, F., Gosse, M. and Parsons, M.P. (2020) The Relationship between Glutamate Dynamics and Activity-Dependent Synaptic Plasticity. Journal of Neurosciences, 40, 2793-2807. https://doi.org/10.1523/JNEUROSCI.1655-19.2020
|
[158]
|
Mameli, M., Zamudio, P.A., Carta, M. and Valenzuela, C.F. (2005) Developmentally Regulated Actions of Alcohol on Hippocampal Glutamatergic Transmission. Journal of Neuroscience 25, 8027-8036. https://doi.org/10.1523/JNEUROSCI.2434-05.2005
|
[159]
|
Bird, C.W., Barber, M.J., Post, H.R., Jacquez, B., Chavez, G.J., Faturos, N.G. and Valenzuela, C.F. (2020) Neonatal Ethanol Exposure Triggers Apoptosis in the Murine Retrosplenial Cortex: Role of Inhibition of NMDA Receptor-Driven Action Potential Firing. Neuropharmacology, 162, Article ID: 107837. https://doi.org/10.1016/j.neuropharm.2019.107837
|
[160]
|
Puglia, M.P. and Valenzuela, C.F (2010) Ethanol Acutely Inhibits Ionotropic Glutamate Receptor-Mediated Responses and Long-Term Potentiation in the Developing CA1 Hippocampus. Alcoholism: Clinical and Experimental Research, 34, 594-606. https://doi.org/10.1111/j.1530-0277.2009.01128.x
|
[161]
|
Cichon, J. and Gan, W.B. (2015) Branch-Specific Dendritic Ca2+ Spikes Cause Persistent Synaptic Plasticity. Nature, 520, 180-185. https://doi.org/10.1038/nature14251
|
[162]
|
Brager, D.H. and Johnston, D. (2014) Channelopathies and Dendritic Dysfunction in Fragile X Syndrome. Brain Research Bulletin, 103, 11-17. https://doi.org/10.1016/j.brainresbull.2014.01.002
|
[163]
|
Rema, V. and Ebner, F.F. (1999) Effect of Enriched Environment Rearing on Impairments in Cortical Excitability and Plasticity after Prenatal Alcohol Exposure. The Journal of Neuroscience, 19, 10993-11006. https://doi.org/10.1523/JNEUROSCI.19-24-10993.1999
|
[164]
|
Savage, D.D., Queen, S.A., Sanchez, C.F., Paxton, L.L., Mahoney, J.C., Goodlett, C.R. and West, J.R. (1992) Prenatal Ethanol Exposure during the Last Third of Gestation in Rat Reduces Hippocampal NMDA Agonist Binding Site Density in 45-Day-Old Offspring. Alcohol, 9, 37-41. https://doi.org/10.1016/0741-8329(92)90007-W
|
[165]
|
Kervern, M., Silvestre de Ferron, B., Alaux-Cantin, S., Fedorenko, O., Antol, J., Naassila, M. and Pierrefiche, O. (2015) Aberrant NMDA-dependent LTD after Perinatal Ethanol Exposure in Young Adult Rat Hippocampus. Hippocampus, 25, 912-923. https://doi.org/10.1002/hipo.22414
|
[166]
|
Ster, J., Steuble, M., Orlando, C., Diep, T.M., Akhmedov, A., Raineteau, O., et al. (2014) Calsyntenin-1 Regulates Targeting of Dendritic NMDA Receptors and Dendritic Spine Maturation in CA1 Hippocampal Pyramidal Cells during Postnatal Development. Neuroscience, 34, 8716-8727. https://doi.org/10.1523/JNEUROSCI.0144-14.2014
|
[167]
|
Möhler, H. (2007) Molecular Regulation of Cognitive Functions and Developmental Plasticity: Impact of GABAA Receptors. Journal of Neurochemistry, 102, 1-12. https://doi.org/10.1111/j.1471-4159.2007.04454.x
|
[168]
|
Wamsley, B. and Fishell, G. (2017) Genetic and Activity-Dependent Mechanisms Underlying Interneuron Diversity. Nature Reviews Neuroscience, 18, 299-309. https://doi.org/10.1038/nrn.2017.30
|
[169]
|
Marin, O. and Rubenstein, J.L. (2001) A Long, Remarkable Journey: Tangential Migration in the Telencephalon. Nature Reviews Neuroscience, 2, 780-790. https://doi.org/10.1038/35097509
|
[170]
|
Lim, L., Mi, D., Llorca, A. and Marin, O. (2018) Development and Functional Diversification of Cortical Interneurons. Neuron, 100, 294-313. https://doi.org/10.1016/j.neuron.2018.10.009
|
[171]
|
Tang, X., Jaenisch, R. and Sur, M. (2021) The Role of GABAergic Signalling in Neurodevelopmental Disorders. Nature Reviews Neuroscience, 22, 290-307. https://doi.org/10.1038/s41583-021-00443-x
|
[172]
|
Francavilla, R., Guet-McCreight, A., Amalyan, S., Hui, C.W., Topolnik, D, Michaud, F., et al. (2020) Alterations in Intrinsic and Synaptic Properties of Hippocampal CA1 VIP Interneurons during Aging. Frontiers in Cellular Neuroscience, 14, Article 554405. https://doi.org/10.3389/fncel.2020.554405
|
[173]
|
Bartolini, G., Ciceri, G. and Marin, O. (2013) Integration of GABAergic Interneurons into Cortical Cell Assemblies: Lessons from Embryos and Adults. Neuron, 79, 849-864. https://doi.org/10.1016/j.neuron.2013.08.014
|
[174]
|
Pfeffer, C.K., Xue, M., He, M., Huang, Z.J. and Scanziani, M. (2013) Inhibition of Inhibition in Visual Cortex: The Logic of Connections between Molecularly Distinct Interneurons. Nature Neuroscience, 16, 1068-1076. https://doi.org/10.1038/nn.3446
|
[175]
|
Skorput, A.G., Gupta, V.P., Yeh, P.W. and Yeh, H.H. (2015) Persistent Interneuronopathy in the Prefrontal Cortex of Young Adult Offspring Exposed to Ethanol in Utero. The Journal of Neuroscience, 35, 10977-10988. https://doi.org/10.1523/JNEUROSCI.1462-15.2015
|
[176]
|
Larsen, Z.H., Chander, P., Joyner, J.A., Floruta, C.M., Demeter, T.L. and Weick, J.P. (2016) Effects of Ethanol on Cellular Composition and Network Excitability of Human Pluripotent Stem Cell-Derived Neurons. Alcoholism: Clinical and Experimental Research, 40, 2339-2350. https://doi.org/10.1111/acer.13218
|
[177]
|
Sirieix, C.M., Tobia, C.M., Schneider, R.W. and Darnall, R.A. (2015) Impaired Arousal in Rat Pups with Prenatal Alcohol Exposure Is Modulated by GABAergic Mechanisms. Physiological Reports, 3, e12424. https://doi.org/10.14814/phy2.12424 https://pubmed.ncbi.nlm.nih.gov/26059034/
|
[178]
|
Valenzuela, C.F. and Jotty, K. (2015) Effects of Ethanol on GABAA Receptor-Mediated Neurotransmission in the Cerebellar Cortex—Recent Advances. Cerebellum, 14, 438-446. https://doi.org/10.1007/s12311-014-0639-3
|
[179]
|
Gerace, E., Landucci, E., Totti, A., Bani, D., Guasti, D., Baronti, R., et al. (2016) Ethanol Toxicity during Brain Development, Alterations of Excitatory Synaptic transmission in Immature Organotypic Hippocampal Slice Cultures. Alcoholism: Clinical and Experimental Research, 40, 706-716. https://doi.org/10.1111/acer.13006
|
[180]
|
Joseph, J., Warton, C., Jacobson, S.W., Jacobson, J.L., Molteno, C.D., Eicher, A., et al. (2014) Three-Dimensional Surface Deformation-Based Shape Analysis of Hippocampus and Caudate Nucleus in Children with Fetal Alcohol Spectrum Disorders. Hum Brain Mapping, 35, 659-672. https://doi.org/10.1002/hbm.22209
|
[181]
|
Delgado-García, J.M. (2001) Structure and Function of the Cerebellum. Revue Neurologique, 33, 635-642. https://doi.org/10.33588/rn.3307.2001305
|
[182]
|
Servais, L., Hourez, R., Bearzatto, B., Gall, D., Schiffmann, S.N. and Cheron, G. (2007) Purkinje Cell Dysfunction and Alteration of Long-Term Synaptic Plasticity in Fetal Alcohol Syndrome. Proceedings of the National Academy of Sciences of the United States of America, 104, 9858-9863. https://doi.org/10.1073/pnas.0607037104
|
[183]
|
Luo, J. (2015) Effects of Ethanol on the Cerebellum: Advances and Prospects. Cerebellum, 14, 383-385. https://doi.org/10.1007/s12311-015-0674-8
|
[184]
|
Light, K.E., Hayar A.M. and Dwight, R. (2015) Electrophysiological and Immunohistochemical Evidence for an Increase in GABAergic Inputs and HCN Channels in Purkinje Cells that Survive Developmental Ethanol Exposure. Cerebellum, 14, 398-412. https://doi.org/10.1007/s12311-015-0651-2
|
[185]
|
Chertoff, M. (2015) Protein Malnutrition and Brain Development. Brain Disorders and Therapy, 4. https://doi.org/10.4172/2168-975X.1000171
|
[186]
|
Rushmore, R.J., McGaughy, J.A., Mokler, D.J. and Rosene, D.L. (2020) The Enduring Effect of Prenatal Protein Malnutrition on Brain Anatomy, Physiology and Behavior. Nutritional Neuroscience, 1-8. https://doi.org/10.1080/1028415X.2020.1859730
|
[187]
|
Darbinian, N. and Selzer, M.E. (2022) Oligodendrocyte Pathology in Fetal Alcohol Spectrum Disorders. Neural Regeneration Research, 17, 497-502. https://doi.org/10.4103/1673-5374.314294
|
[188]
|
Cantacorps, L., Alfonso-Loeches, S., Moscoso-Castro, M., Cuitavi, J., Gracia-Rubio, I., López-Arnau, R., et al. (2017) Maternal Alcohol Binge Drinking Induces Persistent Neuroinflammation Associated with Myelin Damage and Behavioural Dysfunctions in Offspring Mice. Neuropharmacology, 123, 368-384. https://doi.org/10.1016/j.neuropharm.2017.05.034
|
[189]
|
Chiappelli, F., Taylor, A.N., Espinosa de los Monteros, A., de Vellis, J. (1991) Fetal Alcohol Delays the Developmental Expression of Myelin Basic Protein and Transferrin in Rat Primary Oligodendrocyte Cultures. International Journal of Developmental Neuroscience, 9, 67-75. https://doi.org/10.1016/0736-5748(91)90074-V
|
[190]
|
Newville, J., Valenzuela, C.F., Li, L., Jantzie, L.L. and Cunningham, L.A. (2017) Acute Oligodendrocyte Loss with Persistent White Matter Injury in a Third Trimester Equivalent Mouse Model of Fetal Alcohol Spectrum Disorder. Glia, 65, 1317-1332. https://doi.org/10.1002/glia.23164
|
[191]
|
Kwon, O.S., Schmued, L.C. and Slikker Jr., W. (1997) Fumonisin B1 in Developing Rats Alters Brain Sphinganine Levels and Myelination. Neurotoxicology, 18, 571-579.
|
[192]
|
Mandal, C., Park, J.H., Lee, H.T., Seo, H., Chung, I.Y., Choi, I.G., et al. (2015) Reduction of Nfia Gene Expression and Subsequent Target Genes by Binge Alcohol in the Fetal Brain. Neuroscience Letters, 598, 73-78. https://doi.org/10.1016/j.neulet.2015.05.016
|
[193]
|
Tong, M., Yu, R., Silbermann, E., Zabala, V., Deochand, C. and de la Monte, S.M. (2015) Differential Contributions of Alcohol and Nicotine-Derived Nitrosamine Ketone (NNK) to White Matter Pathology in the Adolescent Rat Brain. Alcohol and Alcoholism, 50, 680-689. https://doi.org/10.1093/alcalc/agv102
|
[194]
|
Crespi, C., Galandra, C., Canessa, N., Manera, M., Poggi, P. and Basso, G. (2020) Microstructural Damage of White-Matter Tracts Connecting Large-Scale Networks Is Related to Impaired Executive Profile in Alcohol Use Disorder. Neuroimage: Clinical, 25, Article ID: 102141. https://doi.org/10.1016/j.nicl.2019.102141
|
[195]
|
Sullivan, E.V., Rohlfing, T. and Pfefferbaum, A. (2010) Quantitative Fiber Tracking of Lateral and Interhemispheric White Matter Systems in Normal Aging: Relations to Timed Performance. Neurobiology of Aging, 31, 464-481. https://doi.org/10.1016/j.neurobiolaging.2008.04.007
|
[196]
|
McEvoy, L.K., Fennema-Notestine, C., Elman, J.A., Eyler, L.T., Franz, C.E., Hagler Jr., D.J., et al. (2018) Alcohol Intake and Brain White Matter in Middle Aged Men: Microscopic and Macroscopic Differences. Neuroimage: Clinical, 18, 390-398. https://doi.org/10.1016/j.nicl.2018.02.006
|
[197]
|
Pfefferbaum, A., Rosenbloom, M., Rohlfing, T. and Sullivan, E.V. (2009) Degradation of Association and Projection White Matter Systems in Alcoholism Detected with Quantitative Fiber Tracking. Biological Psychiatry, 65, 680-690. https://doi.org/10.1016/j.biopsych.2008.10.039
|
[198]
|
Fan, J., Meintjes, E.M., Molteno, C.D., Spottiswoode, B.S., Dodge, N.C., Alhamud, A.A., et al. (2015) White Matter Integrity of the Cerebellar Peduncles as a Mediator of Effects of Prenatal Alcohol Exposure on Eyeblink Conditioning. Human Brain Mapping, 36, 2470-2482. https://doi.org/10.1002/hbm.22785
|
[199]
|
Sowell, E.R., Johnson, A., Kan, E., Lu, L.H., Van Horn, J.D., Toga, A.W., et al. (2008) Mapping White Matter Integrity and Neurobehavioral Correlates in Children with Fetal Alcohol Spectrum Disorders. Journal of Neuroscience, 28, 1313-1319. https://doi.org/10.1523/JNEUROSCI.5067-07.2008
|
[200]
|
Gautam, P., Nuñez, S.C., Narr, K.L., Kan, E.C. and Sowell, E.R. (2014) Effects of Prenatal Alcohol Exposure on the Development of White Matter Volume and Change in Executive Function. Neuroimage: Clinical, 5, 19-27. https://doi.org/10.1016/j.nicl.2014.05.010
|
[201]
|
Darbinian, N., Darbinyan, A., Merabova, N., Bajwa, A., Tatevosian, G., Martirosyan, D., et al. (2021) Ethanol-Mediated Alterations in Oligodendrocyte Differentiation in the Developing Brain. Neurobiology of Disease, 148, Article ID: 105181. https://doi.org/10.1016/j.nbd.2020.105181
|
[202]
|
Meintjes, E.M., Narr, K.L., van der Kouwe, A.J., Molteno, C.D., Pirnia T., Gutman B., et al. (2014) A Tensor-Based Morphometry Analysis of Regional Differences in Brain Volume in Relation to Prenatal Alcohol Exposure. Neuroimage: Clinical, 5, 152-160. https://doi.org/10.1016/j.nicl.2014.04.001
|
[203]
|
Lebel, C., Roussotte, F. and Sowell, E.R. (2011) Imaging the Impact of Prenatal Alcohol Exposure on the Structure of the Developing Human Brain. Neuropsychology Review, 21, 102-118. https://doi.org/10.1007/s11065-011-9163-0
|
[204]
|
Feldman, H.S., Jones, K.L., Lindsay, S., Slymen, D., Klonoff-Cohen, H., Kao, K., et al. (2012) Prenatal Alcohol Exposure Patterns and Alcohol-Related Birth Defects and Growth Deficiencies: A Prospective Study. Alcoholism: Clinical and Experimental Research, 36, 670-676. https://doi.org/10.1111/j.1530-0277.2011.01664.x
|
[205]
|
Miller, M.W. (1996) Effect of Early Exposure to Ethanol on the Protein and DNA Contents of Specific Brain Regions in the Rat. Brain Research, 734, 286-294. https://doi.org/10.1016/0006-8993(96)00651-8
|
[206]
|
Webster, W.S., Walsh, D.A., Lipson, A.H. and McEwen, S.E. (1980) Teratogenesis after Acute Alcohol Exposure in Inbred and Outbred Mice. Neurobehavioral Toxicology and Teratology, 2, 227-234.
|
[207]
|
Miller, M.W. and Robertson, S. (1993) Prenatal Exposure to Ethanol Alters the Postnatal Development and Transformation of Radial Glia to Astrocytes in the Cortex. Journal of Comparative Neurology, 337, 253-266. https://doi.org/10.1002/cne.903370206
|
[208]
|
Miller, M.W. and Luo, J. (2002) Effects of Ethanol and Transforming Growth Factor Beta (TGF beta) on Neuronal Proliferation and nCAM Expression. Alcoholism: Clinical and Experimental Research, 26, 1281-1285. https://doi.org/10.1097/00000374-200208000-00022
|
[209]
|
Siegenthaler, J.A. and Miller, M.W. (2005) Ethanol Disrupts Cell Cycle Regulation in Developing Rat Cortex Interaction with Transforming Growth Factor β1. Journal of Neurochemistry, 95, 902-912. https://doi.org/10.1111/j.1471-4159.2005.03461.x
|
[210]
|
Watari, H., Born, D.E. and Gleason, C.A. (2006) Effects of First Trimester Binge Alcohol Exposure on Developing White Matter in Fetal Sheep. Pediatric Research, 59, 560-564. https://doi.org/10.1203/01.pdr.0000203102.01364.de
|
[211]
|
Silvestre de Ferron, B., Bennouar, K.E., Kervern, M., Alaux-Cantin, S., Robert, A., Rabiant, K., et al. (2015) Two Binges of Ethanol a Day Keep the Memory Away in Adolescent Rats, Key Role for GLUN2B Subunit. The International Journal of Neuropsychopharmacology, 19, No.1. https://doi.org/10.1093/ijnp/pyv087
|
[212]
|
Adiong, J.P., Kim, E., Koren, G. and Bozzo, P. (2014) Consuming Non-Alcoholic Beer and Other Beverages during Pregnancy and Breastfeeding. Canadian Family Physician, 60, 724-725. http://www.ncbi.nlm.nih.gov/pmc/articles/pmc4131961/
|
[213]
|
Olguin, S.L., Thompson, S.M., Young, J.W. and Brigman, J.L. (2021) Moderate Prenatal Alcohol Exposure Impairs Cognitive Control, but Not Attention, on a Rodent Touchscreen Continuous Performance Task. Genes Brain Behavior, 20, e12652. https://doi.org/10.1111/gbb.12652
|
[214]
|
Wieczorek, L., Fish, E.W., O’Leary-Moore, S.K., Parnell, S.E. and Sulik, K.K. (2015) Hypothalamic-Pituitary-Adrenal Axis and Behavioral Dysfunction following Early Binge-Like Prenatal Alcohol Exposure in Mice. Alcohol, 49, 207-217. https://doi.org/10.1016/j.alcohol.2015.01.005
|
[215]
|
Konovalov, H.V., Kovetsky, N.S., Bobryshev, Y.V. and Ashwell, K.W. (1997) Disorders of Brain Development in the Progeny of Mothers Who Used Alcohol during Pregnancy. Early Human Development, 48, 153-166. https://doi.org/10.1016/S0378-3782(96)01848-8
|