代谢组学
微生物群
肠道菌群
代谢组
砷
肠道微生物群
生物
代谢途径
鞘脂
代谢物
新陈代谢
脂质代谢
砷毒性
生物信息学
生物化学
化学
有机化学
作者
Jingchuan Xue,Yunjia Lai,Liang Chi,Pengcheng Tu,Jiapeng Leng,Chih‐Wei Liu,Hongyu Ru,Kun Lü
标识
DOI:10.1021/acs.jproteome.8b00697
摘要
Arsenic contamination in drinking water has been a worldwide health concern for decades. In addition to being a well-recognized carcinogen, arsenic exposure has also been linked to diabetes, neurological effects, and cardiovascular diseases. Recently, increasing evidence has indicated that gut microbiome is an important risk factor in modulating the development of diseases. We aim to investigate the role of gut microbiome perturbation in arsenic-induced diseases by coupling a mass-spectrometry-based metabolomics approach and an animal model with altered gut microbiome induced by bacterial infection. Serum metabolic profiling has revealed that gut microbiome perturbation and arsenic exposure induced the dramatic changes of numerous metabolite pathways, including fatty acid metabolism, phospholipids, sphingolipids, cholesterols, and tryptophan metabolism, which were not or were less disrupted when the gut microbiome stayed normal. In summary, this study suggests that gut microbiome perturbation can exacerbate or cause metabolic disorders induced by arsenic exposure.
科研通智能强力驱动
Strongly Powered by AbleSci AI