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膳食诱导的肠道早熟对大鼠出生后时期盲肠微生物群及其与血脑屏障的关系的影响。

Impact of dietary induced precocious gut maturation on cecal microbiota and its relation to the blood-brain barrier during the postnatal period in rats.

机构信息

Food for Health Science Center, Lund University Kemicentrum, Lund, Sweden.

Department of Biology, Lund University, Lund, Sweden.

出版信息

Neurogastroenterol Motil. 2018 Jun;30(6):e13285. doi: 10.1111/nmo.13285. Epub 2018 Jan 12.

DOI:10.1111/nmo.13285
PMID:29327435
Abstract

BACKGROUND

Precocious maturation of the gastrointestinal barrier (GIB) in newborn mammals can be induced by dietary provocation, but how this affects the gut microbiota and the gut-brain axis remains unknown. The objective of this study was to investigate effects of induced GIB maturation on gut microbiota composition and blood-brain barrier (BBB) permeability.

METHODS

Suckling rats were studied at 72 h after gavage with phytohemagglutinin (PHA) or microbial protease (PT) to induce maturation of GIB. For comparison, untreated suckling and weaned rats were included (n = 10). Human serum albumin (HSA) was administered orally and analyzed in blood to assess permeability of the GIB, while intraperitoneally injected bovine serum albumin (BSA) was measured in the brain tissue for BBB permeability. The cecal microbial composition, plasma lipopolysaccharide-binding protein (LBP) levels and short-chain fatty acids in serum and brain were analyzed.

KEY RESULTS

Cessation of HSA passage to blood after PHA or PT treatment was similar to that seen in weaned rats. Interestingly, concomitant increases in cecal Bacteroidetes and plasma LBP levels were observed after both PHA and PT treatments. The BBB passage of BSA was surprisingly elevated after weaning, coinciding with lower plasma LBP levels and specific microbial taxa and increased acetate uptake into the brain.

CONCLUSIONS & INFERENCES: This study provides evidence that the gut microbiota alteration following induced precocious GIB maturation may induce low-grade systemic inflammation and alter SCFAs utilization in the brain which may also play a potential role in GIB-BBB dysfunction disorders in neonates.

摘要

背景

新生哺乳动物胃肠道屏障(GIB)的早熟可以通过饮食刺激来诱导,但这如何影响肠道微生物群和肠-脑轴尚不清楚。本研究的目的是研究诱导的 GIB 成熟对肠道微生物群组成和血脑屏障(BBB)通透性的影响。

方法

在灌胃植物血球凝集素(PHA)或微生物蛋白酶(PT)后 72 小时研究哺乳大鼠,以诱导 GIB 成熟。为了比较,还包括未处理的哺乳和断奶大鼠(n=10)。口服给予人血清白蛋白(HSA)并在血液中分析以评估 GIB 的通透性,而腹腔内注射牛血清白蛋白(BSA)并在脑组织中测量以评估 BBB 的通透性。分析盲肠微生物组成、血浆脂多糖结合蛋白(LBP)水平以及血清和脑组织中的短链脂肪酸。

主要结果

PHA 或 PT 处理后 HSA 停止向血液传递与断奶大鼠相似。有趣的是,在 PHA 和 PT 处理后均观察到盲肠拟杆菌和血浆 LBP 水平同时升高。断奶后,BSA 的 BBB 通透性出人意料地升高,同时血浆 LBP 水平降低,特定微生物类群增加,以及大脑中乙酸盐摄取增加。

结论

本研究提供的证据表明,诱导的 GIB 早熟后肠道微生物群的改变可能会引起低度全身炎症,并改变大脑中 SCFAs 的利用,这也可能在新生儿 GIB-BBB 功能障碍障碍中发挥潜在作用。

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