利用核磁共振成像生物标志物研究自闭症大鼠模型的脑肠微生物群动态和炎症过程

IF 4.7 2区 医学 Q1 NEUROIMAGING NeuroImage Pub Date : 2024-10-24 DOI:10.1016/j.neuroimage.2024.120899
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引用次数: 0

摘要

自闭症谱系障碍(ASD)的特点是社交互动障碍和重复行为。最近的研究表明,肠道菌群失调可能会导致类似 ASD 的行为。然而,肠道微生物群改变影响 ASD 患者大脑功能和行为的确切发育时间点仍不清楚。我们假设,与 ASD 相关的大脑微结构变化和肠道菌群失调会诱发代谢失调和促炎症反应,从而共同导致幼儿期观察到的社会行为缺陷。我们使用了一种通过产前丙戊酸暴露产生的类似自闭症的大鼠模型。我们利用弥散张量成像(DTI)分析了大脑微观结构的变化,并检查了微生物群、血液和粪便样本中的炎症生物标记物。ASD模型大鼠的前扣带回皮层、海马、纹状体和丘脑出现了显著的脑微结构变化;微生物群多样性(前孢子菌科(Prevotellaceae)和钩端螺旋体科(Peptostreptococcaceae))降低;代谢特征发生了改变。出生后第35天是发育的关键时期,在这一时期观察到的微生物群多样性和密度的变化凸显了早期干预ASD的重要性。我们在 ASD 模型中发现了一种独特的代谢特征,即甲酸盐水平升高,乙酸盐和丁酸盐水平降低,这表明短链脂肪酸 (SCFA) 代谢失调。此外,还观察到星形胶质细胞和小胶质细胞活化增加以及促炎细胞因子-白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、γ干扰素(IFN-γ)和肿瘤坏死因子-α(TNF-α)升高,表明免疫失调。这项研究深入揭示了大脑与肠道之间复杂的相互作用,并指出 DTI 指标是 ASD 潜在的成像生物标志物,从而强调了对儿童早期干预的必要性。
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Investigating brain–gut microbiota dynamics and inflammatory processes in an autistic-like rat model using MRI biomarkers during childhood and adolescence
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.
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来源期刊
NeuroImage
NeuroImage 医学-核医学
CiteScore
11.30
自引率
10.50%
发文量
809
审稿时长
63 days
期刊介绍: NeuroImage, a Journal of Brain Function provides a vehicle for communicating important advances in acquiring, analyzing, and modelling neuroimaging data and in applying these techniques to the study of structure-function and brain-behavior relationships. Though the emphasis is on the macroscopic level of human brain organization, meso-and microscopic neuroimaging across all species will be considered if informative for understanding the aforementioned relationships.
期刊最新文献
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