Cheng Shuohan, Meng Xianyue, Wang Zixuan, Lan Tianfang, Zhou Zhi, Wang Zhonghua, Abliz Zeper
Key Laboratory of Mass Spectrometry Imaging and Metabolomics, Minzu University of China, National Ethnic Affairs Commission, Beijing 100081, China.
Key Laboratory of Ethnomedicine of Ministry of Education, School of Pharmacy, Minzu University of China, Beijing 100081, China.
Metabolites. 2024 Dec 2;14(12):670. doi: 10.3390/metabo14120670.
Diabetic encephalopathy (DE) is a neurological complication of diabetes marked by cognitive decline and complex metabolic disturbances. Salidroside (SAL), a natural compound with antioxidant and neuroprotective properties, has shown promise in alleviating diabetic complications. Exploring the spatial metabolic reprogramming in DE and elucidating SAL's metabolic effects are critical for deepening our understanding of its pathogenesis and developing effective therapeutic strategies. Air-flow-assisted desorption electrospray ionization-mass spectrometry imaging (AFADESI-MSI) was employed to investigate spatial metabolic alterations in the brains of db/db mice, a spontaneous DE model. The mice were treated with SAL (30 and 150 mg/kg, orally) for 12 weeks. Differential metabolites were identified and characterized using high-resolution mass spectrometry and validated against public databases. Our AFADESI-MSI analysis revealed significant changes in 26 metabolites in the brains of DE mice compared to the controls. These metabolic changes indicated disruptions in glucose, glutamate-glutamine, nucleotide, lipid, choline, aspartate, and L-carnitine metabolism. Notably, glucose 6-phosphate (G6P), glutamine, adenosine, L-carnitine, and choline exhibited similar trends in both db/db mice and STZ-induced rat models of DE, suggesting their potential as reliable biomarkers. Twelve weeks of SAL treatment demonstrated a positive regulatory effect on glucose metabolism, the glutamate-glutamine cycle, and lipid metabolism. This study identifies key metabolic alterations in DE and demonstrates the therapeutic potential of SAL in modulating these disturbances, offering valuable insights for targeted interventions in diabetic complications.
糖尿病性脑病(DE)是糖尿病的一种神经并发症,其特征为认知功能下降和复杂的代谢紊乱。红景天苷(SAL)是一种具有抗氧化和神经保护特性的天然化合物,已显示出缓解糖尿病并发症的潜力。探索DE中的空间代谢重编程并阐明SAL的代谢作用,对于深化我们对其发病机制的理解和制定有效的治疗策略至关重要。采用气流辅助解吸电喷雾电离质谱成像(AFADESI-MSI)技术研究了自发DE模型db/db小鼠大脑中的空间代谢变化。小鼠口服SAL(30和150 mg/kg),持续12周。使用高分辨率质谱对差异代谢物进行鉴定和表征,并与公共数据库进行比对验证。我们的AFADESI-MSI分析显示,与对照组相比,DE小鼠大脑中有26种代谢物发生了显著变化。这些代谢变化表明葡萄糖、谷氨酸-谷氨酰胺、核苷酸、脂质、胆碱、天冬氨酸和左旋肉碱代谢受到破坏。值得注意的是,磷酸葡萄糖(G6P)、谷氨酰胺、腺苷、左旋肉碱和胆碱在db/db小鼠和链脲佐菌素诱导的DE大鼠模型中表现出相似的趋势,表明它们有潜力成为可靠的生物标志物。12周的SAL治疗对葡萄糖代谢、谷氨酸-谷氨酰胺循环和脂质代谢具有正向调节作用。本研究确定了DE中的关键代谢改变,并证明了SAL在调节这些紊乱方面的治疗潜力,为糖尿病并发症的靶向干预提供了有价值的见解。