Xue Cheng, Chen Jiaxin, Li Xinming, Zhou Chenchen, Mao Zhiguo
Division of Nephrology, Shanghai Changzheng Hospital, Naval Medical University (Second Military Medical University), Shanghai, China.
Outpatient Department, Yangpu Third Military Retreat, Yangpu first retirement, Shanghai, 200000, China.
Biochem Biophys Rep. 2025 Mar 5;42:101967. doi: 10.1016/j.bbrep.2025.101967. eCollection 2025 Jun.
Chronic kidney disease (CKD) often follows acute kidney injury, leading to renal fibrosis and progressive renal failure. Spermine, a polyamine with antioxidant and anti-inflammatory properties, helps reduce renal fibrosis and may serve as a biomarker for CKD progression. We used spatially resolved metabonomic analysis with AFADESI-MSI to examine polyamine distribution in kidneys of a folic acid (FA)-induced CKD mouse model. Results showed decreased spermine and increased spermidine levels, associated with elevated spermine oxidase (SMOX) and spermidine/spermine N1-acetyltransferase (SSAT) enzyme expression in CKD. These findings suggest that altered polyamine metabolism contributes to CKD progression and may provide targets for polyamine-based therapies.
慢性肾脏病(CKD)常继发于急性肾损伤,导致肾纤维化和进行性肾衰竭。精胺是一种具有抗氧化和抗炎特性的多胺,有助于减轻肾纤维化,并可能作为CKD进展的生物标志物。我们使用AFADESI-MSI进行空间分辨代谢组学分析,以研究叶酸(FA)诱导的CKD小鼠模型肾脏中的多胺分布。结果显示,CKD小鼠体内精胺水平降低、亚精胺水平升高,同时精胺氧化酶(SMOX)和亚精胺/精胺N1-乙酰基转移酶(SSAT)的酶表达增加。这些发现表明,多胺代谢改变促成了CKD的进展,并可能为基于多胺的治疗提供靶点。