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Acute Ethanol Exposure During Synaptogenesis Rapidly Alters Medium Spiny Neuron Morphology and Synaptic Protein Expression in the Dorsal Striatum

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2022 Jan 11
PMID 35008713
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Abstract

Fetal alcohol spectrum disorders are caused by the disruption of normal brain development in utero. The severity and range of symptoms is dictated by both the dosage and timing of ethanol administration, and the resulting developmental processes that are impacted. In order to investigate the effects of an acute, high-dose intoxication event on the development of medium spiny neurons (MSNs) in the striatum, mice were injected with ethanol on P6, and neuronal morphology was assessed after 24 h, or at 1 month or 5 months of age. Data indicate an immediate increase in MSN dendritic length and branching, a rapid decrease in spine number, and increased levels of the synaptic protein PSD-95 as a consequence of this neonatal exposure to ethanol, but these differences do not persist into adulthood. These results demonstrate a rapid neuronal response to ethanol exposure and characterize the dynamic nature of neuronal architecture in the MSNs. Although differences in neuronal branching and spine density induced by ethanol resolve with time, early changes in the caudate/putamen region have a potential impact on the execution of complex motor skills, as well as aspects of long-term learning and addictive behavior.

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References
1.
Fernandez-Lizarbe S, Pascual M, Guerri C . Critical role of TLR4 response in the activation of microglia induced by ethanol. J Immunol. 2009; 183(7):4733-44. DOI: 10.4049/jimmunol.0803590. View

2.
Antony J, Paquin A, Nutt S, Kaplan D, Miller F . Endogenous microglia regulate development of embryonic cortical precursor cells. J Neurosci Res. 2011; 89(3):286-98. DOI: 10.1002/jnr.22533. View

3.
Charych E, Akum B, Goldberg J, Jornsten R, Rongo C, Zheng J . Activity-independent regulation of dendrite patterning by postsynaptic density protein PSD-95. J Neurosci. 2006; 26(40):10164-76. PMC: 6674632. DOI: 10.1523/JNEUROSCI.2379-06.2006. View

4.
Wilcox M, Cuzon Carlson V, Sherazee N, Sprow G, Bock R, Thiele T . Repeated binge-like ethanol drinking alters ethanol drinking patterns and depresses striatal GABAergic transmission. Neuropsychopharmacology. 2013; 39(3):579-94. PMC: 3895236. DOI: 10.1038/npp.2013.230. View

5.
Rice J, Suggs L, Lusk A, Parker M, Candelaria-Cook F, Akers K . Effects of exposure to moderate levels of ethanol during prenatal brain development on dendritic length, branching, and spine density in the nucleus accumbens and dorsal striatum of adult rats. Alcohol. 2012; 46(6):577-84. PMC: 3615033. DOI: 10.1016/j.alcohol.2011.11.008. View