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产前酒精暴露后,微生物群和营养作为风险及恢复力因素

Microbiota and nutrition as risk and resiliency factors following prenatal alcohol exposure.

作者信息

Upreti Deepa, Rouzer Siara K, Bowring Abigail, Labbe Emma, Kumar Rosaline, Miranda Rajesh C, Mahnke Amanda H

机构信息

Department of Neuroscience and Experimental Therapeutics, Texas A&M University School of Medicine, Bryan, TX, United States.

出版信息

Front Neurosci. 2023 Jun 15;17:1182635. doi: 10.3389/fnins.2023.1182635. eCollection 2023.

DOI:10.3389/fnins.2023.1182635
PMID:37397440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10308314/
Abstract

Alcohol exposure in adulthood can result in inflammation, malnutrition, and altered gastroenteric microbiota, which may disrupt efficient nutrient extraction. Clinical and preclinical studies have documented convincingly that prenatal alcohol exposure (PAE) also results in persistent inflammation and nutrition deficiencies, though research on the impact of PAE on the enteric microbiota is in its infancy. Importantly, other neurodevelopmental disorders, including autism spectrum and attention deficit/hyperactivity disorders, have been linked to gut microbiota dysbiosis. The combined evidence from alcohol exposure in adulthood and from other neurodevelopmental disorders supports the hypothesis that gut microbiota dysbiosis is likely an etiological feature that contributes to negative developmental, including neurodevelopmental, consequences of PAE and results in fetal alcohol spectrum disorders. Here, we highlight published data that support a role for gut microbiota in healthy development and explore the implication of these studies for the role of altered microbiota in the lifelong health consequences of PAE.

摘要

成年期饮酒会导致炎症、营养不良以及胃肠微生物群改变,这可能会干扰营养物质的有效摄取。临床和临床前研究已令人信服地证明,产前酒精暴露(PAE)也会导致持续的炎症和营养缺乏,不过关于PAE对肠道微生物群影响的研究尚处于起步阶段。重要的是,其他神经发育障碍,包括自闭症谱系障碍和注意力缺陷多动障碍,都与肠道微生物群失调有关。成年期饮酒以及其他神经发育障碍的综合证据支持了这样一种假说,即肠道微生物群失调可能是一种病因特征,它会导致包括神经发育在内的PAE的负面发育后果,并导致胎儿酒精谱系障碍。在此,我们重点介绍支持肠道微生物群在健康发育中起作用的已发表数据,并探讨这些研究对微生物群改变在PAE终身健康后果中所起作用的启示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/709f/10308314/7a918cc44798/fnins-17-1182635-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/709f/10308314/7a918cc44798/fnins-17-1182635-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/709f/10308314/7a918cc44798/fnins-17-1182635-g001.jpg

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本文引用的文献

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Nat Rev Dis Primers. 2023 Feb 23;9(1):11. doi: 10.1038/s41572-023-00420-x.
2
Fetal anemia and elevated hepcidin in a mouse model of fetal alcohol spectrum disorder.胎儿酒精谱系障碍小鼠模型中的胎儿贫血和铁调素升高。
Pediatr Res. 2023 Aug;94(2):503-511. doi: 10.1038/s41390-023-02469-6. Epub 2023 Jan 26.
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The diversity of the intestinal microbiota in patients with alcohol use disorder and its relationship to alcohol consumption and cognition.酒精使用障碍患者肠道微生物群的多样性及其与酒精消费和认知的关系。
发育性酒精暴露使人疲惫不堪:睡眠与发育过程中酒精暴露的持久后果。
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Molecular Markers in Maternal Blood Exosomes Allow Early Detection of Fetal Alcohol Spectrum Disorders.母体外周血 exosomes 中的分子标志物可早期检测胎儿酒精谱系障碍。
Int J Mol Sci. 2022 Dec 21;24(1):135. doi: 10.3390/ijms24010135.
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Dose-related shifts in proteome and function of extracellular vesicles secreted by fetal neural stem cells following chronic alcohol exposure.慢性酒精暴露后胎儿神经干细胞分泌的细胞外囊泡蛋白质组和功能的剂量相关变化。
Heliyon. 2022 Nov 1;8(11):e11348. doi: 10.1016/j.heliyon.2022.e11348. eCollection 2022 Nov.
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Intestinal epithelial stem cell transplants as a novel therapy for cerebrovascular stroke.肠道上皮干细胞移植作为一种治疗脑血管中风的新疗法。
Brain Behav Immun. 2023 Jan;107:345-360. doi: 10.1016/j.bbi.2022.10.015. Epub 2022 Oct 31.
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Fetal Alcohol Spectrum Disorder and Iron Homeostasis.胎儿酒精谱系障碍与铁稳态。
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Prenatal alcohol exposure exacerbates acute sensorimotor deficits and impedes long-term behavioral recovery from the effects of an adult-onset cerebrovascular ischemic stroke.产前酒精暴露会加重急性感觉运动缺陷,并阻碍成年后发生脑血管缺血性中风后长期行为恢复。
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