Department of Physiology, School of Medicine, College of Medicine & Health, University College Cork, Cork, Ireland; Department of Anatomy & Neuroscience, School of Medicine, College of Medicine & Health, University College Cork, Cork, Ireland; APC Microbiome Ireland, University College Cork, Cork, Ireland.
Department of Physiology, School of Medicine, College of Medicine & Health, University College Cork, Cork, Ireland.
EBioMedicine. 2019 Jun;44:618-638. doi: 10.1016/j.ebiom.2019.03.029. Epub 2019 Mar 18.
It is increasingly evident that perturbations to the diversity and composition of the gut microbiota have significant consequences for the regulation of integrative physiological systems. There is growing interest in the potential contribution of microbiota-gut-brain signalling to cardiorespiratory control in health and disease.
In adult male rats, we sought to determine the cardiorespiratory effects of manipulation of the gut microbiota following a 4-week administration of a cocktail of antibiotics. We subsequently explored the effects of administration of faecal microbiota from pooled control (vehicle) rat faeces, given by gavage to vehicle- and antibiotic-treated rats.
Antibiotic intervention depressed the ventilatory response to hypercapnic stress in conscious animals, owing to a reduction in the respiratory frequency response to carbon dioxide. Baseline frequency, respiratory timing variability, and the expression of apnoeas and sighs were normal. Microbiota-depleted rats had decreased systolic blood pressure. Faecal microbiota transfer to vehicle- and antibiotic-treated animals also disrupted the gut microbiota composition, associated with depressed ventilatory responsiveness to hypercapnia. Chronic antibiotic intervention or faecal microbiota transfer both caused significant disruptions to brainstem monoamine neurochemistry, with increased homovanillic acid:dopamine ratio indicative of increased dopamine turnover, which correlated with the abundance of several bacteria of six different phyla.
Chronic antibiotic administration and faecal microbiota transfer disrupt gut microbiota, brainstem monoamine concentrations and the ventilatory response to hypercapnia. We suggest that aberrant microbiota-gut-brain axis signalling has a modulatory influence on respiratory behaviour during hypercapnic stress. FUND: Department of Physiology and APC Microbiome Ireland, University College Cork, Ireland.
越来越多的证据表明,肠道微生物群的多样性和组成的改变对整合生理系统的调节有重大影响。人们对微生物群-肠道-大脑信号在健康和疾病中的心肺控制中的潜在作用越来越感兴趣。
在成年雄性大鼠中,我们试图确定在给予抗生素鸡尾酒 4 周后,对肠道微生物群进行操作的心肺效应。随后,我们通过灌胃给予来自对照组(载体)大鼠粪便的粪便微生物群,探索了其对载体和抗生素处理大鼠的影响。
抗生素干预使清醒动物对高碳酸血症应激的通气反应受到抑制,这归因于二氧化碳对呼吸频率的反应减少。基础频率、呼吸时间变异性以及无呼吸和叹息的表达正常。微生物群耗竭的大鼠收缩压降低。粪便微生物群转移到载体和抗生素处理的动物也破坏了肠道微生物群的组成,与对高碳酸血症的通气反应性降低有关。慢性抗生素干预或粪便微生物群转移都导致脑干单胺神经化学物质的显著破坏,增加的高香草酸:多巴胺比值表明多巴胺周转率增加,这与六个不同门的几种细菌的丰度相关。
慢性抗生素给药和粪便微生物群转移破坏了肠道微生物群、脑干单胺浓度和对高碳酸血症的通气反应。我们认为,异常的微生物群-肠道-大脑轴信号对高碳酸血症应激期间的呼吸行为具有调节作用。 基金:爱尔兰科克大学学院生理学系和 APC 微生物组爱尔兰。