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Updated: May 16, 2025

Strategies for Assessing Autistic-Like Behaviors in Mice
Published on: September 20, 2024
Lactobacillus paracasei-derived extracellular vesicles reverse molecular and behavioral deficits in mouse models of
Jin-Young Park1, Eun-Hwa Lee1, Ji-Eun Kim2
1Department of Brain and Cognitive Sciences, Scranton College, Ewha Womans University, Seoul, Republic of Korea.
Insights
Extracellular vesicles from Lactobacillus paracasei (LpEV) show promise in treating autism spectrum disorder (ASD) symptoms. LpEVs improved social behaviors and reduced repetitive actions in genetic ASD mouse models, suggesting a novel therapeutic avenue.
Area of Science:
- Neuroscience
- Microbiology
- Genetics
Background:
- Autism spectrum disorder (ASD) is a complex neurodevelopmental condition with limited effective treatments.
- Extracellular vesicles from Lactobacillus paracasei (LpEV) have demonstrated neuroprotective properties.
- Genetic mouse models offer valuable insights into ASD mechanisms and potential therapeutic interventions.
Purpose of the Study:
- To investigate the efficacy of LpEVs in ameliorating core symptoms of ASD in genetic mouse models.
- To explore the molecular mechanisms underlying LpEVs' therapeutic effects in ASD.
- To identify potential therapeutic targets for ASD treatment.
Main Methods:
- Treatment of Dopamine receptor D2 (Drd2)-knockout mice with LpEVs.
- Behavioral assessments to evaluate social deficits and repetitive behaviors.
- RNA sequencing and Gene Ontology enrichment analysis of brain tissue.
- Investigating LpEV efficacy in Oxytocin receptor (Oxtr)-knockout heterozygous, adenylyl cyclase-5 knockout, and Shank3-knockout mice.
Main Results:
- LpEV treatment significantly improved autistic-like behaviors in Drd2-knockout mice.
- RNA sequencing revealed LpEVs reversed gene expression alterations in the brains of Drd2-knockout mice, with significant overlap with known ASD genes.
- LpEVs also improved behaviors in Oxtr-knockout heterozygous, adenylyl cyclase-5 knockout, and Shank3-knockout mouse models.
Conclusions:
- LpEVs demonstrate significant therapeutic potential for reversing ASD-related signaling pathway dysregulation and improving core symptoms.
- LpEVs may offer a broad therapeutic strategy for ASD by targeting multiple pathways.
- Further research into LpEVs as a treatment for ASD is warranted.
Abstract:
Autism spectrum disorder (ASD) is a heterogeneous group of neurodevelopmental disorders characterized by social communication deficits and repetitive behaviors. Although our current understanding the mechanisms underlying ASD is growing, effective treatment options are still underdevelopment. Extracellular vesicles derived from the probiotic Lactobacillus paracasei (LpEV) have shown neuroprotective effects in both in vitro and in vivo models. Here we investigate whether LpEV can alleviate core symptoms in genetic ASD models that exhibit accumulated developmental deficits. Dopamine receptor D2 (Drd2)-knockout (KO) mice exhibit social behavior deficits and excessive grooming, core symptoms of ASD. LpEV treatment significantly improves these autistic-like behaviors in Drd2-KO mice, suggesting that LpEVs can mitigate the persistent dysregulation of signaling pathways in these mice. RNA sequencing followed by Gene Ontology enrichment analysis of LpEV-treated Drd2-KO mice identifies distinct groups of genes altered in the brain of Drd2-KO mice, which were reversed by LpEV treatment. Notably, a high proportion of these genes overlap significantly with known ASD genes in the SFARI database, strengthening the potential of LpEV to target relevant pathways in ASD. Further investigation identifies oxytocin and oxytocin receptor (Oxtr) as potential therapeutic targets. LpEV treatment significantly improves autistic-like behaviors in Oxtr-KO heterozygous mice, adenylyl cyclase-5 KO mice and Shank3-KO mice, suggesting its therapeutic potential to target ASD through broader mechanisms beyond a single gene pathway. These results highlight the therapeutic potential of LpEV in reversing the accumulated dysregulated signaling pathways leading to ASD symptoms and improving autistic-like behaviors.

