Journal Article

Investigating brain–gut microbiota dynamics and inflammatory processes in an autistic-like rat model using MRI biomarkers during childhood and adolescence

Tseng, Hsin-Yi, Li, Ssu-Ju, Chang, Ching-Wen, Palanivelu, Lalitha, Liang, Yao-Wen, Lo, Yu-Chun, Chang, Chih-Ju, Chen, You-Yin

2024

Overview

•Reduced microbiota diversity emphasized the early interventions targeting gut dysbiosis in ASD.•Dysregulation in SCFA metabolism potentially impacts ASD-related behaviors.•Elevated astrocytic, microglial activation, and proinflammatory cytokines in ASD.•The potential of DTI metrics as imaging-based biomarkers for ASD. Autism spectrum disorder (ASD) is characterized by social interaction deficits and repetitive behaviors. Recent research has linked that gut dysbiosis may contribute to ASD-like behaviors. However, the exact developmental time point at which gut microbiota alterations affect brain function and behavior in patients with ASD remains unclear. We hypothesized that ASD-related brain microstructural changes and gut dysbiosis induce metabolic dysregulation and proinflammatory responses, which collectively contribute to the social behavioral deficits observed in early childhood. We used an autistic-like rat model that was generated via prenatal valproic acid exposure. We analyzed brain microstructural changes using diffusion tensor imaging (DTI) and examined microbiota, blood, and fecal samples for inflammation biomarkers. The ASD model rats exhibited significant brain microstructural changes in the anterior cingulate cortex, hippocampus, striatum, and thalamus; reduced microbiota diversity (Prevotellaceae and Peptostreptococcaceae); and altered metabolic signatures. The shift in microbiota diversity and density observed at postnatal day (PND) 35, which is a critical developmental period, underscored the importance of early ASD interventions. We identified a unique metabolic signature in the ASD model, with elevated formate and reduced acetate and butyrate levels, indicating a dysregulation in short-chain fatty acid (SCFA) metabolism. Furthermore, increased astrocytic and microglial activation and elevated proinflammatory cytokines—interleukin-1 beta (IL-1β), interleukin-6 (IL-6), interferon-gamma (IFN-γ), and tumor necrosis factor-alpha (TNF-α)—were observed, indicating immune dysregulation. This study provided insights into the complex interplay between the brain and the gut, and indicated DTI metrics as potential imaging-based biomarkers in ASD, thus emphasizing the need for early childhood interventions.

• Publisher: Elsevier Inc,Elsevier Limited,Elsevier
• Subject: Acetic acid / Adolescence / Animals / Anisotropy / Autism / Autism spectrum disorder / Autism Spectrum Disorder - diagnostic imaging / Autism Spectrum Disorder - immunology / Autism Spectrum Disorder - metabolism / Autism Spectrum Disorder - microbiology / Behavior / Biomarkers / Biomarkers - metabolism / Brain - diagnostic imaging / Brain - metabolism / Brain research / Brain-Gut Axis - physiology / Childhood / Children / Chromatography / Cortex (cingulate) / Cytokines / Developmental stages / Diffusion tensor imaging / Diffusion Tensor Imaging - methods / Disease Models, Animal / Dysbacteriosis / Fatty acids / Feces / Female / Gastrointestinal Microbiome / Gut microbiota / Gut-brain axis / Immune system / Inflammation / Inflammation - diagnostic imaging / Inflammation - metabolism / Interleukin 1 / Interleukin 6 / Intestinal microflora / Magnetic resonance imaging / Magnetic Resonance Imaging - methods / Male / Mass spectrometry / Metabolites / Microbiome dysbiosis / Microbiota / Neostriatum / Neurodevelopmental disorders / Neuroimaging / Neuroinflammation / Pregnancy / Prenatal experience / Prenatal exposure / Rats / Rats, Sprague-Dawley / Scientific imaging / Social behavior / Tumor necrosis factor-α / Valproic acid / Valproic Acid - pharmacology / γ-Interferon