Khattri Ram B, Thome Trace, Ryan Terence E
Department of Applied Physiology and Kinesiology, University of Florida, Gainesville, FL 32611, USA.
Center for Exercise Science, University of Florida, Gainesville, FL 32611, USA.
Metabolites. 2021 Jan 10;11(1):45. doi: 10.3390/metabo11010045.
Chronic kidney disease (CKD) results in the impaired filtration of metabolites, which may be toxic or harmful to organs/tissues. The objective of this study was to perform unbiased H nuclear magnetic resonance (NMR)-based metabolomics profiling of tissues from mice with CKD. Five-month-old male C57BL6J mice were placed on either a casein control diet or adenine-supplemented diet to induce CKD for 24 weeks. CKD was confirmed by significant increases in blood urea nitrogen (24.1 ± 7.7 vs. 105.3 ± 18.3 mg/dL, < 0.0001) in adenine-fed mice. Following this chronic adenine diet, the kidney, heart, liver, and quadriceps muscles were rapidly dissected; snap-frozen in liquid nitrogen; and the metabolites were extracted. Metabolomic profiling coupled with multivariate analyses confirm clear separation in both aqueous and organic phases between control and CKD mice. Severe energetic stress and apparent impaired mitochondrial metabolism were observed in CKD kidneys evidenced by the depletion of ATP and NAD, along with significant alterations in tricarboxylic acid (TCA) cycle intermediates. Altered amino acid metabolism was observed in all tissues, although significant differences in specific amino acids varied across tissue types. Taken together, this study provides a metabolomics fingerprint of multiple tissues from mice with and without severe CKD induced by chronic adenine feeding.
慢性肾脏病(CKD)会导致代谢产物滤过受损,这些代谢产物可能对器官/组织有毒或有害。本研究的目的是对患有CKD的小鼠组织进行基于氢核磁共振(NMR)的无偏代谢组学分析。将5个月大的雄性C57BL6J小鼠置于酪蛋白对照饮食或补充腺嘌呤的饮食中,诱导CKD 24周。通过腺嘌呤喂养小鼠的血尿素氮显著升高(24.1±7.7对105.3±18.3mg/dL,<0.0001)证实了CKD。在这种慢性腺嘌呤饮食后,迅速解剖肾脏、心脏、肝脏和股四头肌;在液氮中速冻;并提取代谢产物。代谢组学分析结合多变量分析证实,对照小鼠和CKD小鼠在水相和有机相均有明显分离。在CKD肾脏中观察到严重的能量应激和明显的线粒体代谢受损,表现为ATP和NAD耗竭,以及三羧酸(TCA)循环中间体的显著改变。在所有组织中均观察到氨基酸代谢改变,尽管特定氨基酸的显著差异因组织类型而异。综上所述,本研究提供了慢性腺嘌呤喂养诱导的重度CKD小鼠和未患重度CKD小鼠多种组织的代谢组学指纹图谱。