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富含 n-3 的母体饮食可重编程后代的神经血管转录组,并减轻内毒素诱导的新生儿炎症。

Maternal n-3 enriched diet reprograms the offspring neurovascular transcriptome and blunts inflammation induced by endotoxin in the neonate.

机构信息

Institute of Neuroscience and Physiology, Centre of Perinatal Medicine and Health, Sahlgrenska Academy, University of Gothenburg, Box 432, Gothenburg, 405 30, Sweden.

Department of Pediatrics, University of California Irvine, Irvine, CA, USA.

出版信息

J Neuroinflammation. 2024 Aug 11;21(1):199. doi: 10.1186/s12974-024-03191-8.

Abstract

Infection during the perinatal period can adversely affect brain development, predispose infants to ischemic stroke and have lifelong consequences. We previously demonstrated that diet enriched in n-3 polyunsaturated fatty acids (n-3 PUFA) transforms brain lipid composition in the offspring and protects the neonatal brain from stroke, in part by blunting injurious immune responses. Critical to the interface between the brain and systemic circulation is the vasculature, endothelial cells in particular, that support brain homeostasis and provide a barrier to systemic infection. Here, we examined whether maternal PUFA-enriched diets exert reprograming of endothelial cell signalling in postnatal day 9 mice after modeling aspects of infection using LPS. Transcriptome analysis was performed on microvessels isolated from brains of pups from dams maintained on 3 different maternal diets from gestation day 1: standard, n-3 enriched or n-6 enriched diets. Depending on the diet, in endothelial cells LPS produced distinct regulation of pathways related to immune response, cell cycle, extracellular matrix, and angiogenesis. N-3 PUFA diet enabled higher immune reactivity in brain vasculature, while preventing imbalance of cell cycle regulation and extracellular matrix cascades that accompanied inflammatory response in standard diet. Cytokine analysis revealed a blunted LPS response in blood and brain of offspring from dams on n-3 enriched diet. Analysis of cerebral vasculature in offspring in vivo revealed no differences in vessel density. However, vessel complexity was decreased in response to LPS at 72 h in standard and n-6 diets. Thus, LPS modulates specific transcriptomic changes in brain vessels of offspring rather than major structural vessel characteristics during early life. N-3 PUFA-enriched maternal diet in part prevents an imbalance in homeostatic processes, alters inflammation and ultimately mitigates changes to the complexity of surface vessel networks that result from infection. Importantly, maternal diet may presage offspring neurovascular outcomes later in life.

摘要

围产期感染会对大脑发育产生不良影响,使婴儿易患缺血性中风,并产生终身影响。我们之前的研究表明,富含 n-3 多不饱和脂肪酸 (n-3 PUFA) 的饮食可以改变后代的大脑脂质组成,并保护新生儿大脑免受中风的影响,部分原因是抑制了有害的免疫反应。大脑和全身循环之间的关键界面是血管,特别是内皮细胞,它们支持大脑的内环境稳定,并为全身感染提供屏障。在这里,我们研究了母体 PUFA 丰富的饮食是否会在模拟 LPS 感染的某些方面后,对产后第 9 天的幼鼠内皮细胞信号通路进行重新编程。我们对来自母体饮食为标准、n-3 丰富或 n-6 丰富的母鼠的后代大脑中小血管中分离的微血管进行了转录组分析。根据饮食的不同,LPS 在与免疫反应、细胞周期、细胞外基质和血管生成相关的通路中产生了不同的调节作用。n-3 PUFA 饮食使大脑血管的免疫反应能力增强,同时防止标准饮食中伴随炎症反应的细胞周期调节和细胞外基质级联失衡。细胞因子分析显示,来自 n-3 丰富饮食的母鼠后代的 LPS 反应减弱。体内幼鼠大脑血管分析显示,血管密度没有差异。然而,在标准和 n-6 饮食中,LPS 在 72 小时时会降低血管复杂性。因此,LPS 调节了后代大脑血管的特定转录组变化,而不是在生命早期调节主要的血管结构特征。富含 n-3 PUFA 的母体饮食部分防止了内稳态过程的失衡,改变了炎症,并最终减轻了感染导致的表面血管网络复杂性的变化。重要的是,母体饮食可能预示着后代以后的神经血管结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f61/11316986/7e2886d41379/12974_2024_3191_Fig1_HTML.jpg

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