Department of Pharmacy, Clinical Medical College, and Affiliated Hospital of Chengdu University, Chengdu, Sichuan 610081, China.
Department of Nuclear Medicine, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan 610072, China.
J Environ Pathol Toxicol Oncol. 2021;40(4):43-52. doi: 10.1615/JEnvironPatholToxicolOncol.2021039409.
The disease progression of rheumatoid arthritis (RA) is closely related to the disorder of amino acids metabolism. This study aimed to clarify the changes in the categories, quantities and metabolic pathways of amino acids associated with disease progression in adjuvant-induced arthritis (AIA) rats, and to evaluate the application value of amino acids metabolic profiling in the diagnosis of RA. A total of 20 rats were randomized into a control group and AIA model group. Thirty-three days after modeling, the synovial tissues of left ankle joints were collected for histopathological examination. Also, untargeted metabolomics based on UPLC-LTQ/Orbitrap MS was used to identify the potential amino acids and analyze the changes of their metabolic pathways. Histopathological observation showed that the synovial tissues of AIA rats exhibited hyperplastic and inflammatory lesions. Through multivariate statistical analysis, a total of 12 amino acids were identified and considered to show metabolic changes in AIA rats. Compared with the control group, the concentrations of glutamate, arginine, methionine were increased in the AIA model group; while the concentrations of proline, valine, tyrosine, phenylalanine, leucine, glycine, tryptophan, histidine, threonine were decreased. Metabolic pathway analysis showed that the selected amino acids had important physiological functions in immune and inflammatory response. The results suggested that amino acids could be employed as biomarkers closely related to RA, and the analysis of amino acids metabolic profiling also exhibited potential application value in the diagnosis, disease progression monitoring and therapy of RA.
类风湿关节炎(RA)的疾病进展与氨基酸代谢紊乱密切相关。本研究旨在阐明与佐剂诱导关节炎(AIA)大鼠疾病进展相关的氨基酸类别、数量和代谢途径的变化,并评估氨基酸代谢谱分析在 RA 诊断中的应用价值。将 20 只大鼠随机分为对照组和 AIA 模型组。建模 33 天后,取左侧踝关节滑膜组织进行组织病理学检查。同时,采用基于 UPLC-LTQ/Orbitrap MS 的非靶向代谢组学方法鉴定潜在氨基酸,并分析其代谢途径的变化。组织病理学观察显示,AIA 大鼠的滑膜组织表现出增生性和炎症性病变。通过多变量统计分析,共鉴定出 12 种氨基酸,认为其在 AIA 大鼠中存在代谢变化。与对照组相比,AIA 模型组谷氨酸、精氨酸、蛋氨酸浓度升高;而脯氨酸、缬氨酸、酪氨酸、苯丙氨酸、亮氨酸、甘氨酸、色氨酸、组氨酸、苏氨酸浓度降低。代谢途径分析表明,所选氨基酸在免疫和炎症反应中具有重要的生理功能。结果表明,氨基酸可以作为与 RA 密切相关的生物标志物,氨基酸代谢谱分析在 RA 的诊断、疾病进展监测和治疗中也具有潜在的应用价值。