Sarah W. Stedman Nutrition and Metabolism Center, Duke Molecular Physiology Institute, Duke University Medical Center, Durham, North Carolina; Division of Endocrinology, Metabolism, and Nutrition, Department of Medicine, Duke University Medical Center, Durham, North Carolina.
Center for Translational Research in Aging and Longevity, Department of Health and Kinesiology, Texas A&M University, College Station, Texas.
Am J Pathol. 2019 Sep;189(9):1797-1813. doi: 10.1016/j.ajpath.2019.05.021.
Sepsis is a multiorgan disease affecting the ileum and jejunum (small intestine), liver, skeletal muscle, and lung clinically. The specific metabolic changes in the ileum, jejunum, liver, skeletal muscle, and lung have not previously been investigated. Live Pseudomonas aeruginosa, isolated from a patient, was given via i.v. catheter to pigs to induce severe sepsis. Eighteen hours later, ileum, jejunum, medial gastrocnemius skeletal muscle, liver, and lung were analyzed by nontargeted metabolomics analysis using gas chromatography/mass spectrometry. The ileum and the liver demonstrated significant changes in metabolites involved in linoleic acid metabolism: the ileum and lung had significant changes in the metabolism of valine/leucine/isoleucine; the jejunum, skeletal muscle, and liver had significant changes in arginine/proline metabolism; and the skeletal muscle and lung had significant changes in aminoacyl-tRNA biosynthesis, as analyzed by pathway analysis. Pathway analysis also identified changes in metabolic pathways unique for different tissues, including changes in the citric acid cycle (jejunum), β-alanine metabolism (skeletal muscle), and purine metabolism (liver). These findings demonstrate both overlapping metabolic pathways affected in different tissues and those that are unique to others and provide insight into the metabolic changes in sepsis leading to organ dysfunction. This may allow therapeutic interventions that focus on multiple tissues or single tissues once the relationship of the altered metabolites/metabolism to the underlying pathogenesis of sepsis is determined.
败血症是一种多器官疾病,临床上会影响回肠和空肠(小肠)、肝脏、骨骼肌和肺。以前没有研究过回肠、空肠、肝脏、骨骼肌和肺的特定代谢变化。从一名患者身上分离出活铜绿假单胞菌,通过静脉导管给予猪,以诱导严重败血症。18 小时后,通过气相色谱/质谱联用的非靶向代谢组学分析,分析回肠、空肠、中腓肠肌骨骼肌、肝脏和肺。回肠和肝脏的亚油酸代谢相关代谢物发生显著变化:回肠和肺的缬氨酸/亮氨酸/异亮氨酸代谢发生显著变化;空肠、骨骼肌和肝脏的精氨酸/脯氨酸代谢发生显著变化;骨骼肌和肺的氨酰-tRNA 生物合成发生显著变化,通过途径分析。途径分析还确定了不同组织中独特的代谢途径的变化,包括柠檬酸循环(空肠)、β-丙氨酸代谢(骨骼肌)和嘌呤代谢(肝脏)的变化。这些发现不仅表明不同组织中存在重叠的代谢途径,还表明存在其他组织特有的代谢途径,并深入了解导致器官功能障碍的败血症的代谢变化。一旦确定了改变的代谢物/代谢与败血症潜在发病机制的关系,这可能允许针对多种组织或单个组织的治疗干预。