Early developmental changes in GABAA receptor expression in nucleus accumbens medium spiny neurons

The expression of GABA<sub>A</sub>Rs goes through large scale, evolutionarily conserved changes through the early postnatal period. While these changes have been well-studied in brain regions such as the hippocampus and sensory cortices, less is known about early developmental changes in other brain areas. The nucleus accumbens (NAc) is a major hub in the circuitry that mediates motivated behaviors and disruptions in NAc activity is a part of the neuropathology observed in mood and substance use disorders. Considering the importance of early developmental disruptions in the vulnerability to and etiology of these disorders, it is essential to understand normal developmental changes in the NAc as a first step to understanding how these changes might be disrupted to cause long-term pathology. Here, we aimed to address the gap in knowledge of early developmental changes in GABA<sub>A</sub>R expression in NAc neurons. We investigated the expression patterns of GABA<sub>A</sub>R α1, α2, and α4 subunits in Drd1+, Drd2+, and putative hybrid medium spiny neurons (MSNs) of the mouse NAc over a developmental window from P2 to P16. Our findings show a consistent increase in expression of all 3 GABA<sub>A</sub>R subunits in Drd1+ MSNs, accompanied by stable expression or even a decrease in expression in Drd2+ MSNs. The putative hybrid population showed a complex expression pattern, usually showing maximum expression at P9. These early developmental changes likely suggest a specific window where GABA<sub>A</sub>R expression patterns adjust to increasing glutamatergic inputs from external sources, changes in intracellular chloride concentrations, and a switch towards the mature, bistable activity patterns of MSNs from the immature, relatively excitable singular pattern. We propose that this time of dynamic changes in GABA<sub>A</sub>R expression could represent a sensitive period during which developmental insults might lead to permanent disruptions in GABA<sub>A</sub>R expression patterns.

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Publication Details

Journal
Frontiers in Neuroscience
Published
2024-12-12
DOI
https://doi.org/10.3389/fnins.2024.1445162
Citations
1
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
0.27

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article

Early developmental changes in GABAA receptor expression in nucleus accumbens medium spiny neurons

Oluwarotimi Folorunso, Sabina Berretta, Elif Engin, Ziyi Wang et al.
1 citations
Frontiers in Neuroscience
Neuroscience and Neuropharmacology Research
0.27
article

Early developmental changes in GABAA receptor expression in nucleus accumbens medium spiny neurons

Oluwarotimi Folorunso, Sabina Berretta, Elif Engin, Ziyi Wang, Kiely Morris
article en
1 citations

Abstract

The expression of GABA<sub>A</sub>Rs goes through large scale, evolutionarily conserved changes through the early postnatal period. While these changes have been well-studied in brain regions such as the hippocampus and sensory cortices, less is known about early developmental changes in other brain areas. The nucleus accumbens (NAc) is a major hub in the circuitry that mediates motivated behaviors and disruptions in NAc activity is a part of the neuropathology observed in mood and substance use disorders. Considering the importance of early developmental disruptions in the vulnerability to and etiology of these disorders, it is essential to understand normal developmental changes in the NAc as a first step to understanding how these changes might be disrupted to cause long-term pathology. Here, we aimed to address the gap in knowledge of early developmental changes in GABA<sub>A</sub>R expression in NAc neurons. We investigated the expression patterns of GABA<sub>A</sub>R α1, α2, and α4 subunits in Drd1+, Drd2+, and putative hybrid medium spiny neurons (MSNs) of the mouse NAc over a developmental window from P2 to P16. Our findings show a consistent increase in expression of all 3 GABA<sub>A</sub>R subunits in Drd1+ MSNs, accompanied by stable expression or even a decrease in expression in Drd2+ MSNs. The putative hybrid population showed a complex expression pattern, usually showing maximum expression at P9. These early developmental changes likely suggest a specific window where GABA<sub>A</sub>R expression patterns adjust to increasing glutamatergic inputs from external sources, changes in intracellular chloride concentrations, and a switch towards the mature, bistable activity patterns of MSNs from the immature, relatively excitable singular pattern. We propose that this time of dynamic changes in GABA<sub>A</sub>R expression could represent a sensitive period during which developmental insults might lead to permanent disruptions in GABA<sub>A</sub>R expression patterns.

Frontiers in NeuroscienceVol. 18
Harvard University (US), McLean Hospital (US)
National Institute of Child Health and Human Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Good health and well-being
Openalex Percentile: Top 41%
Neuroscience and Neuropharmacology Research
0.27
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