Extracellular space diffusion analysis in the infant and adult rat striatum using magnetic resonance imaging

International Journal of Developmental Neuroscience

Volumn 53, Issue , 2016, Pages 1-7

  Yang, Shuangfeng ^a   Wang, Yan ^a   Li, Kai ^b   Tang, Xiaolu ^a   Zhang, Kuo ^c   Shi, Chunyan ^d,e   Han, Hongbin ^d,e   Peng, Yun ^a  

^a CAPITAL MEDICAL UNIVERSITY   (China)

^b Beijing Jishuitan Hospital   (China)

^c PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

^d PEKING UNIVERSITY THIRD HOSPITAL   (China)

^e Key Lab of Magnetic Resonance Imaging Device and Technique   (China)

Author keywords

Development; Diffusion; Extracellular space; Gd DTPA; Magnetic resonance imaging

Indexed keywords

GADOLINIUM PENTETATE MEGLUMINE; GADOLINIUM PENTETATE; NERVE CELL ADHESION MOLECULE; NERVE PROTEIN; REELIN PROTEIN; SCLEROPROTEIN; SERINE PROTEINASE; TENASCIN;

ADULT; ANIMAL TISSUE; ARTICLE; AXON; CELL TRANSPORT; CLEARANCE; CONTROLLED STUDY; CORPUS STRIATUM; DIFFUSION; DIFFUSION COEFFICIENT; EXTRACELLULAR SPACE; GLIA CELL; INFANT; MALE; METABOLITE; NERVE CELL; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEAR MAGNETIC RESONANCE SCANNER; PERINATAL PERIOD; PRIORITY JOURNAL; RAT; AGE; ANIMAL; CYTOLOGY; DIAGNOSTIC IMAGING; DIET RESTRICTION; GROWTH, DEVELOPMENT AND AGING; METABOLISM; NEWBORN; SPRAGUE DAWLEY RAT; TIME FACTOR; WATER DEPRIVATION;

AGE FACTORS; ANIMALS; ANIMALS, NEWBORN; CELL ADHESION MOLECULES, NEURONAL; CORPUS STRIATUM; EXTRACELLULAR MATRIX PROTEINS; EXTRACELLULAR SPACE; FASTING; GADOLINIUM DTPA; MAGNETIC RESONANCE IMAGING; MALE; NERVE TISSUE PROTEINS; RATS; RATS, SPRAGUE-DAWLEY; SERINE ENDOPEPTIDASES; TENASCIN; TIME FACTORS; WATER DEPRIVATION;

EID: 84976260650     PISSN: 07365748     EISSN: 1873474X     Source Type: Journal    
DOI: 10.1016/j.ijdevneu.2016.05.009     Document Type: Article

References (38)

1. Abbott, N.J., Evidence for bulk flow of brain interstitial fluid: significance for physiology and pathology. Neurochem. Int. 45:4 (2004), 545–552.
2. Badaut, J., Ashwal, S., Adami, A., et al. Brain water mobility decreases after astrocytic aquaporin-4 inhibition using RNA interference. J. Cereb. Blood Flow Metab. 31:3 (2011), 819–831.
3. Binder, D.K., Papadopoulos, M.C., Haggie, P.M., et al. In vivo measurement of brain extracellular space diffusion by cortical surface photobleaching. J. Neurosci. 24:37 (2004), 8049–8056.
4. Bondareff, W., Pysh, J.J., Distribution of the extracellular space during postnatal maturation of rat cerebral cortex. Anat. Rec. 160:4 (1968), 773–780.
5. Caley, D.W., Maxwell, D.S., Development of the blood vessels and extracellular spaces during postnatal maturation of rat cerebral cortex. J. Comp. Neurol. 138:1 (1970), 31–47.
6. Carare, R.O., Bernardes-Silva, M., Newman, T.A., et al. Solutes, but not cells, drain from the brain parenchyma along basement membranes of capillaries and arteries: significance for cerebral amyloid angiopathy and neuroimmunology. Neuropathol. Appl. Neurobiol. 34:2 (2008), 131–144.
7. Celio, M.R., Spreafico, R., De Biasi, S., et al. Perineuronal nets: past and present. Trends Neurosci. 21:12 (1998), 510–515.
8. D'Arcangelo, G., Miao, G.G., Chen, S.C., et al. A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature 374:6524 (1995), 719–723.
9. Erickson, H.P., Tenascin-C, tenascin-R and tenascin-X: a family of talented proteins in search of functions. Curr. Opin. Cell Biol. 5:5 (1993), 869–876.
10. Evers, M.R., Salmen, B., Bukalo, O., et al. Impairment of L-type Ca2+ channel-dependent forms of hippocampal synaptic plasticity in mice deficient in the extracellular matrix glycoprotein tenascin-C. J. Neurosci. 22:16 (2002), 7177–7194.
11. Fenstermacher, J., Kaye, T., Drug diffusion within the brain. Ann N. Y. Acad. Sci. 531 (1988), 29–39.
12. Han, H., Shi, C., Fu, Y., et al. A novel MRI tracer-based method for measuring water diffusion in the extracellular space of the rat brain. IEEE J. Biomed. Health Inform. 18:3 (2014), 978–983.
13. Hartfuss, E., Forster, E., Bock, H.H., et al. Reelin signaling directly affects radial glia morphology and biochemical maturation. Development 130:19 (2003), 4597–4609.
14. Iliff, J.J., Wang, M., Liao, Y., et al. A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid beta. Sci. Transl. Med., 4(147), 2012, 47ra111.
15. Jankovski, A., Sotelo, C., Subventricular zone-olfactory bulb migratory pathway in the adult mouse: cellular composition and specificity as determined by heterochronic and heterotopic transplantation. J. Comp. Neurol. 371:3 (1996), 376–396.
16. Jones, P.L., Jones, F.S., Tenascin-C in development and disease: gene regulation and cell function. Matrix Biol. 19:7 (2000), 581–596.
17. Kunwar, S., Chang, S., Westphal, M., et al. Phase III randomized trial of CED of IL13-PE38QQR vs Gliadel wafers for recurrent glioblastoma. Neuro Oncol. 12:8 (2010), 871–881.
18. Lau LW, C.R., Keough, M.B., et al. Pathophysiology of the brain extracellular matrix: a new target for remyelination. Nat. Rev. Neurosci. 14:10 (2013), 722–729.
19. Lehmenkuhler, A., Sykova, E., Svoboda, J., et al. Extracellular space parameters in the rat neocortex and subcortical white matter during postnatal development determined by diffusion analysis. Neuroscience 55:2 (1993), 339–351.
20. Li, K., Han, H., Zhu, K., et al. Real-time magnetic resonance imaging visualization and quantitative assessment of diffusion in the cerebral extracellular space of C6 glioma-bearing rats. Neurosci. Lett. 543 (2013), 84–89.
21. Liu, B.B.X., Zhou, F., et al. Mutual information based three-dimensional registration of rat brain magnetic resonance imaging time-series. Comput. Electr. Eng. 39:5 (2013), 1473–1484.
22. Lonser, R.R., Sarntinoranont, M., Morrison, P.F., et al. Convection-enhanced delivery to the central nervous system. J. Neurosurg. 122:3 (2015), 697–706.
23. Louveau, A., Smirnov, I., Keyes, T.J., et al. Structural and functional features of central nervous system lymphatic vessels. Nature 523:7560 (2015), 337–341.
24. Michel, G., Tonon, T., Scornet, D., et al. The cell wall polysaccharide metabolism of the brown alga Ectocarpus siliculosus Insights into the evolution of extracellular matrix polysaccharides in Eukaryotes. New Phytol. 188:1 (2010), 82–97.
25. Nicholson, C., Sykova, E., Extracellular space structure revealed by diffusion analysis. Trends Neurosci. 21:5 (1998), 207–215.
26. Nicholson, C., Chen, K.C., Hrabetova, S., et al. Diffusion of molecules in brain extracellular space: theory and experiment. Prog. Brain Res. 125 (2000), 129–154.
27. Nicholson, C., Kamali-Zare, P., Tao, L., Brain extracellular space as a diffusion barrier. Comput. Vis. Sci. 14:7 (2011), 309–325.
28. Nugent, L.J., Jain, R.K., Extravascular diffusion in normal and neoplastic tissues. Cancer Res. 44:1 (1984), 238–244.
29. Saghatelyan, A.K., Dityatev, A., Schmidt, S., et al. Reduced perisomatic inhibition: increased excitatory transmission, and impaired long-term potentiation in mice deficient for the extracellular matrix glycoprotein tenascin-R. Mol. Cell. Neurosci. 17:1 (2001), 226–240.
30. Sandvig, A.B.M., Barrett, L.B., et al. Myelin-, reactive glia-, and scar-derived CNS axon growth inhibitors: expression, receptor signaling, and correlation with axon regeneration. Glia 46:3 (2004), 225–251.
31. Sykova, E., Nicholson, C., Diffusion in brain extracellular space. Physiol. Rev. 88:4 (2008), 1277–1340.
32. Sykova, E., Extracellular space volume and geometry of the rat brain after ischemia and central injury. Adv. Neurol. 73 (1997), 121–135.
33. Sykova, E., Extrasynaptic volume transmission and diffusion parameters of the extracellular space. Neuroscience 129:4 (2004), 861–876.
34. Thorne, R.G., Nicholson, C., In vivo diffusion analysis with quantum dots and dextrans predicts the width of brain extracellular space. Proc. Natl. Acad. Sci. U. S. A. 103:14 (2006), 5567–5572.
35. Xiao, F., Hrabetova, S., Enlarged extracellular space of aquaporin-4-deficient mice does not enhance diffusion of Alexa Fluor 488 or dextran polymers. Neuroscience 161:1 (2009), 39–45.
36. Xie, L., Kang, H., Xu, Q., et al. Sleep drives metabolite clearance from the adult brain. Science 342:6156 (2013), 373–377.
37. Xu, F., Han, H., Zhang, H., et al. Quantification of Gd-DTPA concentration in neuroimaging using T(1)3D MP-RAGE sequence at 3.0T. Magn. Reson. Imaging 29:6 (2011), 827–834.
38. Zuo, L.L.K., Han, H., Comparative analysis by magnetic resonance imaging of extracellular space diffusion and interstitial fluid flow in the rat striatum and thalamus. Appl. Magn. Reson. 46:6 (2015), 623–632.