Liao Wen-Ting, Liu Jie, Zhou Si-Min, Xu Gang, Gao Yu-Qi, Liu Wen-Yuan
Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, China Pharmaceutical University, Nanjing, China.
Institute of Medicine and Hygienic Equipment for High Altitude Region, College of High Altitude Military Medicine, Army Military Medical University, Chongqing, China.
Front Physiol. 2019 Jan 10;9:1950. doi: 10.3389/fphys.2018.01950. eCollection 2018.
Hypoxia appears in a number of extreme environments, including high altitudes, the deep sea, and during aviation, and occurs in cancer, cardiovascular disease, respiratory failures and neurological disorders. Though it is well recognized that hypoxic preconditioning (HPC) exerts endogenous neuroprotective effect against severe hypoxia, the mediators and underlying molecular mechanism for the protective effect are still not fully understood. This study established a hippocampus metabolomics approach to explore the alterations associated with HPC. In this study, an animal model of HPC was established by exposing the adult BALB/c mice to acute repetitive hypoxia four times. Ultra-high liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC-QTOFMS) in combination with univariate and multivariate statistical analyses was employed to deciphering metabolic changes associated with HPC in hippocampus tissue. MetaboAnalyst 3.0 was used to construct HPC related metabolic pathways. The significant metabolic differences in hippocampus between the HPC groups and control were observed, indicating that HPC mouse model was successfully established and HPC could caused significant metabolic changes. Several key metabolic pathways were found to be acutely perturbed, including phenylalanine, tyrosine and tryptophan biosynthesis, taurine and hypotaurine metabolism, phenylalanine metabolism, glutathione metabolism, alanine, aspartate and glutamate metabolism, tyrosine metabolism, tryptophan metabolism, purine metabolism, citrate cycle, and glycerophospholipid metabolism. The results of the present study provided novel insights into the mechanisms involved in the acclimatization of organisms to hypoxia, and demonstrated the neuroprotective mechanism of HPC.
缺氧出现在许多极端环境中,包括高海拔、深海以及航空过程中,也发生于癌症、心血管疾病、呼吸衰竭和神经紊乱等情况。尽管人们已经充分认识到缺氧预处理(HPC)对严重缺氧具有内源性神经保护作用,但其保护作用的介质和潜在分子机制仍未完全明确。本研究建立了一种海马代谢组学方法来探索与HPC相关的变化。在本研究中,通过将成年BALB/c小鼠暴露于急性重复性缺氧四次建立了HPC动物模型。采用超高效液相色谱-四极杆飞行时间质谱(UHPLC-QTOFMS)结合单变量和多变量统计分析来解读海马组织中与HPC相关的代谢变化。使用MetaboAnalyst 3.0构建与HPC相关的代谢途径。观察到HPC组与对照组海马之间存在显著的代谢差异,表明成功建立了HPC小鼠模型,且HPC可引起显著的代谢变化。发现若干关键代谢途径受到急性干扰,包括苯丙氨酸、酪氨酸和色氨酸生物合成、牛磺酸和亚牛磺酸代谢、苯丙氨酸代谢、谷胱甘肽代谢、丙氨酸、天冬氨酸和谷氨酸代谢、酪氨酸代谢、色氨酸代谢、嘌呤代谢、柠檬酸循环和甘油磷脂代谢。本研究结果为生物体适应缺氧的机制提供了新的见解,并证明了HPC的神经保护机制。