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Prebiotic administration modulates gut microbiota and faecal short-chain fatty acid concentrations but does not prevent chronic intermittent hypoxia-induced apnoea and hypertension in adult rats

机译:益生元施用调节肠道微生物酵母和粪便短链脂肪酸浓度,但不能预防成年大鼠中慢性间歇性缺氧诱导的呼吸暂停和高血压

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Background Evidence is accruing to suggest that microbiota-gut-brain signalling plays a regulatory role in cardiorespiratory physiology. Chronic intermittent hypoxia (CIH), modelling human sleep apnoea, affects gut microbiota composition and elicits cardiorespiratory morbidity. We investigated if treatment with prebiotics ameliorates cardiorespiratory dysfunction in CIH-exposed rats. Methods Adult male rats were exposed to CIH (96 cycles/day, 6.0% Osub2/sub at nadir) for 14 consecutive days with and without prebiotic supplementation (fructo- and galacto-oligosaccharides) beginning two weeks prior to gas exposures. Findings CIH increased apnoea index and caused hypertension. CIH exposure had modest effects on the gut microbiota, decreasing the relative abundance of Lactobacilli species, but had no effect on microbial functional characteristics. Faecal short-chain fatty acid (SCFA) concentrations, plasma and brainstem pro-inflammatory cytokine concentrations and brainstem neurochemistry were unaffected by exposure to CIH. Prebiotic administration modulated gut microbiota composition and diversity, altering gut-metabolic (GMMs) and gut-brain (GBMs) modules and increased faecal acetic and propionic acid concentrations, but did not prevent adverse CIH-induced cardiorespiratory phenotypes. Interpretation CIH-induced cardiorespiratory dysfunction is not dependant upon changes in microbial functional characteristics and decreased faecal SCFA concentrations. Prebiotic-related modulation of microbial function and resultant increases in faecal SCFAs were not sufficient to prevent CIH-induced apnoea and hypertension in our model. Our results do not exclude the potential for microbiota-gut-brain axis involvement in OSA-related cardiorespiratory morbidity, but they demonstrate that in a relatively mild model of CIH, sufficient to evoke classic cardiorespiratory dysfunction, such changes are not obligatory for the development of morbidity, but may become relevant in the elaboration and maintenance of cardiorespiratory morbidity with progressive disease. Funding Department of Physiology and APC Microbiome Ireland, University College Cork, Ireland. APC Microbiome Ireland is funded by Science Foundation Ireland, through the Government's National Development Plan.
机译:背景技术证据表明微生物液 - 肠道信号传导在心肺生理学中起着监管作用。慢性间歇性缺氧(CIH),建模人类睡眠呼吸暂停,影响肠道微生物酵母组成,并引发心肺病毒发病率。我们调查了使用益生元的治疗改善CIH暴露大鼠心肺功能障碍。方法将成年雄性大鼠暴露于CIH(96个循环/天,6.0%O 2 在Nadir中连续14天,在此前两周开始两周气体曝光。发现CIH增加的呼吸暂停指数并引起高血压。 CIH暴露对肠道微生物群具有适度的影响,降低了乳杆菌物种的相对丰度,但对微生物功能特性没有影响。粪便短链脂肪酸(SCFA)浓度,血浆和脑干促炎细胞因子浓度和脑干神经化学不受CIH的影响。益生元给药调节肠道微生物群组成和多样性,改变肠道代谢(GMMS)和肠脑(GBMS)模块以及增加的粪便醋酸和丙酸浓度增加,但没有阻止不良CiH诱导的心肺表型。解释CIH诱导的心肺功能障碍不依赖于微生物功能特征的变化和降低粪便SCFA浓度。益生菌相关的微生物功能调节和粪便SCFA的结果增加不足以防止CIH诱导的呼吸暂停和高血压在我们的模型中。我们的结果不排除微生物血肠轴轴的潜力参与OSA相关的心肺发病率,但他们证明,在CIH的相对温和的模型中,足以唤起经典的心肺功能障碍,这种变化不是开发的义务发病率,但在渐进性疾病的培养和维持心肺发病率方面可能变得有关。物资系生理学和APC Microbiome爱尔兰,大学学院科克,爱尔兰。 APC Microbiome Ireland由科学基金会爱尔兰资助,通过政府的国家发展计划。

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