Peterson Veronica L, Jury Nicholas J, Cabrera-Rubio Raúl, Draper Lorraine A, Crispie Fiona, Cotter Paul D, Dinan Timothy G, Holmes Andrew, Cryan John F
APC Microbiome Institute, University College Cork, Cork, Ireland; Department of Anatomy and Neuroscience, University College Cork, Cork, Ireland.
Laboratory of Behavioral and Genomic Neuroscience, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, USA.
Behav Brain Res. 2017 Apr 14;323:172-176. doi: 10.1016/j.bbr.2017.01.049. Epub 2017 Feb 1.
The gut microbiota includes a community of bacteria that play an integral part in host health and biological processes. Pronounced and repeated findings have linked gut microbiome to stress, anxiety, and depression. Currently, however, there remains only a limited set of studies focusing on microbiota change in substance abuse, including alcohol use disorder. To date, no studies have investigated the impact of vapour alcohol administration on the gut microbiome. For research on gut microbiota and addiction to proceed, an understanding of how route of drug administration affects gut microbiota must first be established. Animal models of alcohol abuse have proven valuable for elucidating the biological processes involved in addiction and alcohol-related diseases. This is the first study to investigate the effect of vapour route of ethanol administration on gut microbiota in mice. Adult male C57BL/6J mice were exposed to 4 weeks of chronic intermittent vapourized ethanol (CIE, N=10) or air (Control, N=9). Faecal samples were collected at the end of exposure followed by 16S sequencing and bioinformatic analysis. Robust separation between CIE and Control was seen in the microbiome, as assessed by alpha (p<0.05) and beta (p<0.001) diversity, with a notable decrease in alpha diversity in CIE. These results demonstrate that CIE exposure markedly alters the gut microbiota in mice. Significant increases in genus Alistipes (p<0.001) and significant reductions in genra Clostridium IV and XIVb (p<0.001), Dorea (p<0.01), and Coprococcus (p<0.01) were seen between CIE mice and Control. These findings support the viability of the CIE method for studies investigating the microbiota-gut-brain axis and align with previous research showing similar microbiota alterations in inflammatory states during alcoholic hepatitis and psychological stress.
肠道微生物群包括一群细菌,它们在宿主健康和生物过程中发挥着不可或缺的作用。大量反复的研究发现已将肠道微生物组与压力、焦虑和抑郁联系起来。然而,目前仅有有限的一系列研究关注物质滥用(包括酒精使用障碍)中的微生物群变化。迄今为止,尚无研究调查气态酒精给药对肠道微生物组的影响。为了推进肠道微生物群与成瘾方面的研究,必须首先明确药物给药途径如何影响肠道微生物群。酒精滥用的动物模型已被证明对于阐明成瘾及酒精相关疾病所涉及的生物过程很有价值。这是第一项研究乙醇气态给药途径对小鼠肠道微生物群影响的研究。成年雄性C57BL/6J小鼠暴露于4周的慢性间歇性汽化乙醇(CIE,N = 10)或空气(对照组,N = 9)中。暴露结束时收集粪便样本,随后进行16S测序和生物信息学分析。通过α(p < 0.05)和β(p < 0.001)多样性评估,微生物组中CIE组和对照组之间存在明显分离,CIE组的α多样性显著降低。这些结果表明,CIE暴露显著改变了小鼠的肠道微生物群。与对照组相比,CIE组小鼠中Alistipes属显著增加(p < 0.001),而梭状芽孢杆菌属IV和XIVb(p < 0.001)、Dorea属(p < 0.01)和粪球菌属(p < 0.01)显著减少。这些发现支持了CIE方法在研究微生物群 - 肠道 - 脑轴方面的可行性,并与先前的研究一致,该研究表明在酒精性肝炎和心理压力期间的炎症状态下存在类似的微生物群改变。