代谢物
代谢组学
小肠
急性放射综合征
代谢组
胃肠道
生物
内科学
化学
内分泌学
医学
生物信息学
遗传学
造血
干细胞
作者
Jace W. Jones,Zachary Clifford,Fei Li,Gregory Tudor,Ann M. Farese,Catherine Booth,Thomas J. MacVittie,Maureen A. Kane
出处
期刊:Health Physics
[Lippincott Williams & Wilkins]
日期:2019-01-17
卷期号:116 (4): 473-483
被引量:18
标识
DOI:10.1097/hp.0000000000000955
摘要
High-throughput, targeted metabolomics was used to identify early time-point small intestine and plasma metabolite markers of gastrointestinal acute radiation syndrome. The small intestine metabolite markers were cross correlated to plasma metabolites in order to identify minimally invasive circulating markers. The radiation exposure covered lethal and sublethal gastrointestinal acute radiation syndrome. The small intestine and plasma metabolite profiles were generated at 1 and 3 d postexposure following total-body irradiation. The small intestine and plasma metabolite profiles for mice receiving radiation at day 1 and 3 postexposure were significantly different from sham-irradiated mice. There were 14 metabolite markers identified at day 1 and 18 metabolite markers at day 3 that were small-intestine-specific plasma markers of gastrointestinal acute radiation syndrome. A number of the identified metabolites at day 1 were amino acids. Dysregulation of amino acid metabolism at 24 h post-total-body irradiation provides potential insight into the initial inflammatory response during gastrointestinal acute radiation syndrome.
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