Skip to main content
Log in

Sodium-23 magnetic resonance brain imaging

  • Published:
Neuroradiology Aims and scope Submit manuscript

Summary

This is a review of recent work in23Na MR imaging. The main emphasis of recent papers has been pulse sequences that, with appropriate postprocessing, give images of the fast, slow, and intermediate components of T2 decay. The assignment of compartmental designation to the T2 component remains a problem except for homogeneous structures easily identifiable anatomically (ventricles, superior sagittal sinus, globe of the eye). Compartmental distribution of sodium is described. The predominance of the interstitial and plasma compartment, the invisibility of part of the intracellular sodium, and the difficulty in imaging the very fast T2 component of visible intracellular sodium make the usual Na spin-echo image essentially an image of the interstitial and plasma space. Use of super paramagnetic iron oxide coupled to dextran as a contrast medium may help to identify the plasma compartment. Because the usual Na MR images are essentially interstitial and plasma images, our own interest is in observing functional changes in these compartments. Another proposed application is the detection of the very fast T2 component in brain tumors to aid in defining tumor grade and extent.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Hilal SK, Maudsley AA, Simon HE, Perman WH, Bonn J, Mawad ME, Silver AJ, Ganti SR, Sane P, Chien IC (1983) Invivo NMR imaging of tissue sodium in the intact cat before and after acute cerebral stroke. AJNR 4:245–249

    Google Scholar 

  2. Hilal SK, Maudsley AA, Ra JB, Simon HE, Roschmann P, Wittekoek S, Cho ZH, Mun IK (1985) In vivo NMR imaging of sodium-23 in the human head. J Comput Assist Tomogr 9: 1–7

    Google Scholar 

  3. Perman WH, Turski P, Houston L, Glover GH, Hayes CE (1986) Methodology of in vivo human sodium NMR imaging at 1.5 Tesla. Radiology 160:811–820

    Google Scholar 

  4. Burstein D, Fossel ET (1987) Intracellular sodium and lithium NMR relaxation times in the perfused frog heart. Magn Reson Med 4:261–273

    Google Scholar 

  5. Hilal SK, Ra JB, Oh CH, Mun IK, Einstein SG, Roschmann P (1987) Sodium imaging. In: Stark DD, Bradley WG (eds) Magnetic resonance imaging. Mosby, St. Louis, pp 715–731

    Google Scholar 

  6. Turski PA, Perman WH, Houston L, Winkler SS (1988) Clinical and experimental sodium magnetic resonance imaging. Radiol Clin North Am 26:861–871

    Google Scholar 

  7. Siesjö BK, Deshpande JK (1987) Electrolyte shifts between brain and plasma in hypoglycemic coma. J Cereb Blood Flow Metab 7:789–793

    Google Scholar 

  8. Young W, Rappaport ZH, Chalif DH, Flamm ES (1987) Regional brain sodium, potassium, and water changes in the rat middle cerebral artery occlusion model of ischemia. Stroke 18: 751–759

    Google Scholar 

  9. Levin VA, Fenstermacher JD, Patlak CS (1970) Sucrose and inulin space measurements of the cerebral cortex in four mammalian species. Am J Physiol 219:1528–1533

    Google Scholar 

  10. Pelligrino DA, Musch TI, Dempsey JA (1981) Interregional differences in brain intracellular pH and water compartmentation during acute normoxic and hypoxic hypocapnia in the anesthetized dog. Brain Res 214:387–404

    Google Scholar 

  11. Weiss HR, Buchweitz E, Murtha TJ, Auletta M (1982) Quantitative regional determination of morphometric indices of the total and perfused capillary network in the rat brain. Circ Res 51: 494–503

    Google Scholar 

  12. Sakai AK, Nakazawa K, Tazaki Y, Ishii K, Hino H, Igarashi H, Kanda K (1985) Regional cerebral blood volume and hematocrit measured in normal human volunteers by single photon emission computed tomography. J Cereb Blood Flow Metab 5:207–213

    Google Scholar 

  13. Perman WH, Thomasson DM, Bernstein MA, Turski P (1989) Multiple short echo 2.5 ms quantitation of in vivo sodium T2 relaxation. Magn Reson Med 9:153–160

    Google Scholar 

  14. Ra JB, Hilal SK, Oh CH (1989) An algorithm for magnetic resonance imaging of the short T2 fraction of sodium using the FID signal. J Comput Assist Tomogr 13:1–8

    Google Scholar 

  15. Winkler SS, Thomasson DM, Sherwood K, Perman WH (1989) RegionalT 2 and sodium concentration estimates in the normal human brain by sodium-23 MRI at 1.5 T. J Comput Assit Tomogr 13:561–566

    Google Scholar 

  16. Hilal SK, Oh CH, Mun IK, Johnson G (1989) Grading of gliomas by sodium MRI (abstract). Proc Soc Magn Reson Med, Berkeley, CA, p 83

  17. Gupta RK, Gupta P (1982) Direct observation of resolved resonances from intra and extracellular sodium-23 in NMR studies of intact cells and tissues using dysprosium (III) tripolyphosphate as paramagnetic shift reagent. J Magn Reson 4:344–350

    Google Scholar 

  18. Summers RM, Joseph PM, Renshaw PF, Kundel HL (1988) Dextran magnetite: a contrast agent for sodium-23 MRI. Magn Reson Med 8:427–439

    Google Scholar 

  19. Bogdan A, Lancaster L, Kundel H (1989) Sodium MRI of extravascular lung water using coated magnetite particles (abstract). Proc Soc Magn Reson Med, Berkeley, CA, p 663

  20. Stark DD, Weissleder R, Elizondo G, Hahn PF, Saini S, Todd LE, Wittenberg J, Ferrucci JT (1988) Superparamagnetic iron oxide: clinical application as a contrast agent for MR imaging of the liver. Radiology 168:297–301

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported in part by the Department of Veterans Affairs Medical Research Service

Rights and permissions

Reprints and permissions

About this article

Cite this article

Winkler, S.S. Sodium-23 magnetic resonance brain imaging. Neuroradiology 32, 416–420 (1990). https://doi.org/10.1007/BF00588475

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00588475

Key words

Navigation