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Please use this identifier to cite or link to this item: http://140.112.115.32:8080/ir/handle/987654321/2798

Title:	Generational synaptic functions of GABA A receptor β3 subunit deteriorations in an animal model of social deficit
Authors:	Chu, Ming-Chia;Wu, Han-Fang;Lee, Chi-Wei;Chung, Yueh-Jung;Chi, Hsiang;Chen, Po See;Lin, Hui-Ching
Contributors:	視光學系
Keywords:	Autism spectrum disorder;Excitatory/inhibitory imbalance;GABAAR;Generational effect;Gephyrin;Valproate
Date:	2022-07-01
Issue Date:	2025-08-11 14:44:03 (UTC+8)
Abstract:	Background: Disruption of normal brain development is implicated in numerous psychiatric disorders with neurodevelopmental origins, including autism spectrum disorder (ASD). Widespread abnormalities in brain structure and functions caused by dysregulations of neurodevelopmental processes has been recently shown to exert adverse effects across generations. An imbalance between excitatory/inhibitory (E/I) transmission is the putative hypothesis of ASD pathogenesis, supporting by the specific implications of inhibitory γ-aminobutyric acid (GABA)ergic system in autistic individuals and animal models of ASD. However, the contribution of GABAergic system in the neuropathophysiology across generations of ASD is still unknown. Here, we uncover profound alterations in the expression and function of GABAA receptors (GABAARs) in the amygdala across generations of the VPA-induced animal model of ASD. Methods: The F2 generation was produced by mating an F1 VPA-induced male offspring with naïve females after a single injection of VPA on embryonic day (E12.5) in F0. Autism-like behaviors were assessed by animal behavior tests. Expression and functional properties of GABAARs and related proteins were examined by using western blotting and electrophysiological techniques. Results: Social deficit, repetitive behavior, and emotional comorbidities were demonstrated across two generations of the VPA-induced offspring. Decreased synaptic GABAAR and gephyrin levels, and inhibitory transmission were found in the amygdala from two generations of the VPA-induced offspring with greater reductions in the F2 generation. Weaker association of gephyrin with GABAAR was shown in the F2 generation than the F1 generation. Moreover, dysregulated NMDA-induced enhancements of gephyrin and GABAAR at the synapse in the VPA-induced offspring was worsened in the F2 generation than the F1 generation. Elevated glutamatergic modifications were additionally shown across generations of the VPA-induced offspring without generation difference. Conclusions: Taken together, these findings revealed the E/I synaptic abnormalities in the amygdala from two generations of the VPA-induced offspring with GABAergic deteriorations in the F2 generation, suggesting a potential therapeutic role of the GABAergic system to generational pathophysiology of ASD.
Relation:	Journal of Bionedical Science, 29(1). https://doi.org/10.1186/s12929-022-00835-w
Appears in Collections:	[Department of Optometry] Journal

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