Metabolite aberrations in early diabetes detected in rat kidney using mass spectrometry imaging

被引:35
作者
Bergman, Hilde-Marlene [1 ]
Lindfors, Lina [1 ]
Palm, Fredrik [2 ]
Kihlberg, Jan [1 ]
Lanekoff, Ingela [1 ]
机构
[1] Uppsala Univ, Dept Chem BMC, Box 599, S-75124 Uppsala, Sweden
[2] Uppsala Univ, Dept Med Cell Biol, Box 571, S-75123 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
nano-DESI; Acylcarnitine; Fatty acid oxidation; Branched-chain amino acid; Streptozotocin; Type I diabetes; RENAL LIPID-METABOLISM; PROTEIN-KINASE; FATTY-ACID; ACTIVATION; NEPHROPATHY; DIACYLGLYCEROL; MECHANISM;
D O I
10.1007/s00216-019-01721-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Diabetic kidney disease is a serious complication of diabetes that can ultimately lead to end-stage renal disease. The pathogenesis of diabetic kidney disease is complex, and fundamental research is still required to provide a better understanding of the driving forces behind it. We report regional metabolic aberrations from an untargeted mass spectrometry imaging study of kidney tissue using an insulinopenic rat model of diabetes. Diabetes was induced by intravenous injection of streptozotocin, and kidneys were harvested 2weeks thereafter. Imaging was performed using nanospray desorption electrospray ionization connected to a high-mass-resolving mass spectrometer. No histopathological changes were observed in the kidney sections; however, mass spectrometry imaging revealed a significant increase in several 18-carbon unsaturated non-esterified fatty acid species and monoacylglycerols. Notably, these 18-carbon acyl chains were also constituents of several increased diacylglycerol species. In addition, a number of short- and long-chain acylcarnitines were found to be accumulated while several amino acids were depleted. This study presents unique regional metabolic data indicating a dysregulated energy metabolism in renal mitochondria as an early response to streptozotocin-induced type I diabetes.
引用
收藏
页码:2809 / 2816
页数:8
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