1H-MRS in spinal cord injury: acute and chronic metabolite alterations in rat brain and lumbar spinal cord

被引:22
作者
Erschbamer, Matthias [1 ]
Oberg, Johanna [2 ]
Westman, Eric [3 ]
Sitnikov, Rouslan [2 ,4 ]
Olson, Lars [1 ]
Spenger, Christian [2 ]
机构
[1] Karolinska Inst, Dept Neurosci, SE-17177 Stockholm, Sweden
[2] Karolinska Inst, Dept Clin Sci Intervent & Technol, Div Radiol, SE-14186 Stockholm, Sweden
[3] Karolinska Inst, Dept Neurobiol Hlth Sci & Soc, SE-14186 Stockholm, Sweden
[4] UCL, Inst Neurol, London WC1N 1PJ, England
基金
瑞典研究理事会;
关键词
biochemical profile; experimental spinal cord injury; magnetic resonance; multivariate data analysis; MAGNETIC-RESONANCE-SPECTROSCOPY; VIVO H-1-NMR SPECTROSCOPY; CENTRAL-NERVOUS-SYSTEM; IN-VIVO; N-ACETYLASPARTATE; MR SPECTROSCOPY; VASCULAR MECHANISMS; AXONAL DEGENERATION; REPAIR STRATEGIES; GLIAL SCAR;
D O I
10.1111/j.1460-9568.2010.07562.x
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
A variety of tests of sensorimotor function are used to characterize outcome after experimental spinal cord injury (SCI). These tests typically do not provide information about chemical and metabolic processes in the injured CNS. Here, we used 1H-magnetic resonance spectroscopy (MRS) to monitor long-term and short-term chemical changes in the CNS in vivo following SCI. The investigated areas were cortex, thalamus/striatum and the spinal cord distal to injury. In cortex, glutamate (Glu) decreased 1 day after SCI and slowly returned towards normal levels. The combined glutamine (Gln) and Glu signal was similarly decreased in cortex, but increased in the distal spinal cord, suggesting opposite changes of the Glu/Gln metabolites in cortex and distal spinal cord. In lumbar spinal cord, a marked increase of myo-inositol was found 3 days, 14 days and 4 months after SCI. Changes in metabolite concentrations in the spinal cord were also found for choline and N-acetylaspartate. No significant changes in metabolite concentrations were found in thalamus/striatum. Multivariate data analysis allowed separation between rats with SCI and controls for spectra acquired in cortex and spinal cord, but not in thalamus/striatum. Our findings suggest MRS could become a helpful tool to monitor spatial and temporal alterations of metabolic conditions in vivo in the brain and spinal cord after SCI. We provide evidence for dynamic temporal changes at both ends of the neuraxis, cortex cerebri and distal spinal cord, while deep brain areas appear less affected.
引用
收藏
页码:678 / 688
页数:11
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