Kato K, Ohsaka A, Matsushita K, Yoshikawa K
Biochem Biophys Res Commun. 1987 Apr 14;144(1):53-8. doi: 10.1016/s0006-291x(87)80474-6.
We now report a mouse model system of brain tumor for 31P-NMR spectroscopic study of in vivo cerebral metabolism. In vivo 31P-NMR (109 MHz) spectra were taken on the 9th day by the Faraday shield method of the brain of mice (3-week-old) transplanted intracerebrally with mKS X A tumor cells. In tumor-bearing mice, the amount of creatine phosphate decreased markedly and that of inorganic phosphate plus sugar phosphate increased accordingly. Furthermore, the broadening and splitting of individual signals were also noted with tumor-bearing mice; this is interpreted as indicating a variety of changes in chemical shift occurring in the brain of the animals due to heterogeneous distribution of pH. Binding or detaching of divalent cations to and from phosphometabolites may also be responsible for these changes.
我们现在报告一种脑肿瘤小鼠模型系统,用于对体内脑代谢进行31P核磁共振波谱研究。在第9天,通过法拉第屏蔽法对脑内移植了mKS X A肿瘤细胞的3周龄小鼠的大脑进行体内31P核磁共振(109兆赫)波谱分析。在荷瘤小鼠中,磷酸肌酸的量显著减少,无机磷酸和糖磷酸的量相应增加。此外,还观察到荷瘤小鼠个体信号的变宽和分裂;这被解释为表明由于pH值的不均匀分布,动物大脑中发生了各种化学位移变化。二价阳离子与磷酸代谢物的结合或解离也可能是这些变化的原因。