Abstract
Nuclear magnetic resonance (NMR) is capable of producing anatomical and biochemical data on the brain. Hydrogen-1 [11, 15] exists in abundance in the human body, differs in concentration from one tissue to another, and can be readily detected. Many investigators have therefore used it in tomography [8, 9, 12, 21], and the technique has reached a stage of practical application. However, since only limited biochemical data are available for 1H, the application of 13C, 19F, 31P, and others is being tried. Using 31P-NMR, changes in phosphocreatine, adenosine triphosphate (ATP), sugar phosphates and inorganic phosphate can be determined, but it takes 30-60 min to produce an image. Therefore, 31P-NMR is inadequate for tomography at present. Thus, our aim is to obtain the local spectra of 31P-NMR [1, 13, 26] in vivo in a specified region, utilizing 1H-NMR-CT (computed tomography) as guide, and to establish a biochemical diagnosis of ischemic lesions in the brain. For this purpose, we conducted a fundamental study, in which alterations in phosphorus metabolism were investigated by 31P-NMR spectrometry of the rat ischemic brain and the hypoxic brain, as shown in the sections “In Vitro Study” and “In Vivo Study.” In addition, we are now working on 31P-MRI as shown in the section headed “MRI of 31P”. These works will be mentioned in this order.
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Kogure, K., Ohtomo, H., Matsui, S., Kohno, H. (1985). Aims on Phosphorus-31 Magnetic Resonance Imaging. In: Heiss, WD. (eds) Functional Mapping of the Brain in Vascular Disorders. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-70720-9_3
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DOI: https://doi.org/10.1007/978-3-642-70720-9_3
Publisher Name: Springer, Berlin, Heidelberg
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