Baslow, M. H. 2000. Canavan's spongiform leukodystrophy: A clinical anatomy of a genetic metabolic CNS disease—An analytical review. J. Mol. Neurosci. 15:61–69.
Google Scholar
Moreno, A., Ross, B. D., and Bluml, S. 2001. Direct determination of the N-acetyl-L-aspartate synthesis rate in the human brain by 13C MRS and [1-13C] glucose infusion. J. Neurochem. 77:347–350.
Google Scholar
Baslow, M. H. 2002. Evidence supporting a role for N-acetyl-L-aspartate as a molecular water pump in myelinated neurons in the central nervous system: An analytical review. Neurochem. Int. 40:295–300.
Google Scholar
Baslow, M. H. and Resnik, T. R. 1997. Canavan disease: Analysis of the nature of the metabolic lesions responsible for development of the observed clinical symptoms. J. Mol. Neurosci. 9:109–126.
Google Scholar
Kitada, K., Akimitsu, T., Shigematsu, Y., Kondo, A., Maihara, T., Yokoi, N., Kuramoto, T., Sasa, M., and Serikawa, T. 2000. Accumulation of N-acetyl-L-aspartate in the brain of the tremor rat, a mutant exhibiting absence-like seizure and spongiform degeneration in the central nervous system. J. Neurochem. 74: 2512–2519.
Google Scholar
Tahmaz, F. E., Sam, S., Hoganson, G. E., and Quan, F. 2001. A partial deletion of the aspartoacylase gene is the cause of Canavan disease in a family from Mexico. J. Med. Genet. 38:E9.2(online).
Google Scholar
Matalon, R., Rady, P. L., Platt, K. A., Skinner, H. B., Quast M. J., Campbell, G. A. et al. 2000. Knock-out mouse for Canavan disease: A model for gene transfer to the central nervous system. J. Gene Med. 2:165–175.
Google Scholar
Martin, E., Capone, A., Schneider, J., Hennig, J., and Thiel, T. 2001. Absence of N-acetylaspartate in the human brain: Impact on neurospectroscopy? Ann. Neurol. 49:518–521.
Google Scholar
Baslow, M. H. 1997. A review of phylogenetic and metabolic relationships between the acylamino acids, N-acetyl-L-aspartic acid and N-acetyl-L-histidine in the vertebrate nervous system. J. Neurochem. 68:1335–1344.
Google Scholar
Choi, I.-Y. and Gruetter, R. 2001. In vivo 13C NMR measurement of total brain glycogen concentrations in the conscious rat. Proc. Intl. Soc. Mag. Reson. Med. 9:210.
Google Scholar
Tsai, G. and Coyle, J. T. 1995. N-Acetylaspartate in neuropsychiatric disorders. Prog. Neurobiol. 46:531–540.
Google Scholar
Jung, R. E., Brooks, W. M., Yeo, R. A., Chiulli, S. J., Weers, D. C., and Sibbitt, L. 1999. Biochemical markers of intelligence: A proton MR spectroscopy study of normal human brain. Proc. R. Soc. Lond. B, 266:1375–1379.
Google Scholar
Jung, R. E., Yeo, R. A., Chiulli, S. J., Sibbitt, L., and Brooks, W. M. 2000. Myths of neuropsychology: Intelligence, neurometabolism and cognitive ability. Clin. Neuropsychol. 14:535–545.
Google Scholar
Nicholson, C. and Sykova, E. 1998. Extracellular space structure revealed by diffusion analysis. Trends Neurosci. 21:207–215.
Google Scholar
Pfeuffer, J., Tkac, I., and Gruetter, R. 2000. Extracellular-intracellular distribution of glucose and lactate in the rat brain assessed noninvasively by diffusion-weighted 1H nuclear magnetic resonance spectroscopy in vivo. J. Cereb. Blood Flow Metab. 20:736–746.
Google Scholar
Sager, T. N., Fink-Jensen, A., and Hansen, A. J. 1997. Transient elevation of interstitial N-acetylasparate in reversible global brain ischemia. J. Neurochem. 68:675–682.
Google Scholar
Goldstein, F. B. 1976. Amidohydrolases of brain: Enzymatic hydrolysis of N-acetyl-L-asparatate and other N-acyl-L-amino acids. J. Neurochem. 26:45–49.
Google Scholar
Sager, T. N., Thomsen, C., Valsborg, J. S., Laursen, H., and Hansen, A. J. 1999. Astroglia contain a specific transport mechanism for N-acetyl-L-aspartate. J. Neurochem. 73:807–811.
Google Scholar
Signoretti, S., Marmarou, A., Tavazzi, B., Lazzarino, G., Beaurnont, A., and Vagnozzi, R. 2001. N-Acetylaspartate reduction as a measure on injury severity and mitochondrial dysfunction following diffuse traumatic injury. J. Neurotrauma 18:977–991.
Google Scholar
Bhakoo, K. K., Craig, T. J., and Styles, P. 2001. Developmental and regional distribution of aspartoacylase in rat brain. J. Neurochem. 79:211–220.
Google Scholar
Huang, W., Wang, H., Kekuda, R., Fei, Y., Friedrich, A., Wang, J., et al. 2000. Transport of N-acetyasparate by Na+-dependent high-affinity dicarboxylate transporter NaDC3 and its relevance to the expression of the transporter in the brain. J. Pharmacol. Exp. Therapeut. 295:392–403.
Google Scholar
Baslow, M. H., Suckow, R., Sapirstein, V., and Hungund, B. L. 1999. Expression of aspartoacylase activity in cultured rat macroglial cells is limited to oligodendrocytes. J. Mol. Neurosci. 13:47–53.
Google Scholar
Baslow, M. H., Suckow, R. F., Berg, M. J., Marks, N., Saito, M., and Bhakoo, K. K. 2001. Differential expression of carnosine, homocarnosine and N-acetyl-L-histidine hydrolytic activities in cultured rat macroglial cells. J. Mol. Neurosci. 17:87–95.
Google Scholar
Chakraborty, G., Mekala, P., Yahya, D., Wu, G., and Ledeen, R. W. 2001. Intraneural N-acetylaspartate supplies acetyl groups for myelin lipid synthesis: Evidence for myelin-associated aspartoacylase. J. Neurochem. 78:736–745.
Google Scholar
Kunnecke, B., Cerdannn, S., and Seelig, J. 1993. Cerebral metabolism of [1,2-13C2] glucose and [U-13C4] 3-hydroxybutyrate in rat brain as detected by 13C NMR spectroscopy. NMR Biomed. 6:264–277.
Google Scholar
Warringa, R. A. J., Hoeben, R. C., Koper, J. W., Sykes, J. E. C., van Golde, L. M. G., and Lopes-Cardozo, M. 1987. Hydrocortisone stimulates the development of oligodendrocytes in primary glial cultures and affects glucose metabolism and lipid synthesis in these cultures. Dev. Br. Res. 34:79–86.
Google Scholar
van der Pal, R. H. M., Koper, J. W., van Golde, L. M. G., and Lopes-Cardozo, M. 1988. Effects of insulin-like growth factor (IGF-I) on oligodendrocyte-enriched glial cultures. J. Neurosci. Res. 19:483–490.
Google Scholar
Sonnewald, U., Akiho, H., Koshiya, K., and Iwai, A. 1998. Effect of orotic acid on the metabolism of cerebral cortical astrocytes during hypoxia and reoxygenation: An NMR spectroscopy study. J. Neurosci. Res. 51:103–108.
Google Scholar
Lear, J. L. and Ackermann, R. F. 1990. Evaluation of radio-labeled acetate and fluoracetate as potential tracers of cerebral oxidative metabolism. Metab. Br. Dis. 5:45–56.
Google Scholar
Birken, D. L. and Oldendorf, W. H. 1989. N-acetyl-L-aspartic acid: A literature review of a compound prominent in H-NMR spectroscopic studies of brain. Neurosci. Biobehav. Rev. 13: 23–31.
Google Scholar
Burlina, A. P., Ferrari, V., Facci, L., Skaper, S. D., and Burlina, A. B. 1997. Mast cells contain large quantities of the secretagogue-sensitive N-acetylasparate. J. Neurochem. 69:1314–1317.
Google Scholar
Baslow, M. H. and Yamada, S. 1997. Identification of N-acetylaspartate in the lens of the vertebrate eye: A new model for the investigation of the function of N-acetylated amino acids in vertebrates. Exp. Eye Res. 64:283–286.
Google Scholar
Pouwels, P. J. W., Brockkmann, K., Kruse, B., Wilken, B., Wick, M., Hanefeld, F., and Frahm, J. 1999. Regional age dependence of human brain metabolites from infancy to adulthood as detected by quantitative localized proton MRS. Pediatr. Res. 46:474–485.
Google Scholar
Baslow, M. H. 2000. Functions of N-acetyl-L-aspartate and N-acetyl-L-aspartylglutamate in the vertebrate brain: Role in glial cell-specific signaling. J. Neurochem. 75:453–459.
Google Scholar
Davies, S. E. C., Gotoh, M., Richards, D. A., and Obrenovitch, T. P. 1998. Hypoosmolarity induces an increase in extracellular N-acetylaspartate concentration in the rat striatum. Neurochem. Res. 23:1021–1025.
Google Scholar
Attwell, D. and Laughlin, S. B. 2001. An energy budget for signaling in the grey matter of the brain. J. Cereb. Blood Flow Metab. 21:1133–1145.
Google Scholar
Le Bihan, D., Turner, R., and Douek, P. 1993. Is water diffusion restricted in human brain white matter? An echo-planar NMR imaging study. Neuroreport 4:887–890.
Google Scholar
Mackert, B. M., Staub, F., Baethmann, A., and Kempski, O. 1996. Anoxia in vitro does not induce neuronal swelling or death. J. Neurol. Sci. 139:39–47.
Google Scholar
Baslow, M. H. 1998. Function of the N-acetyl-L-histidine system in the vertebrate eye: Evidence in support of a role as a molecular water pump. J. Mol. Neurosci. 10:193–208.
Google Scholar
Baslow, M. H. 1999. The existence of molecular water pumps in the nervous system: A review of the evidence. Neurochem. Int. 34:77–90.
Google Scholar
Meinild, A.-K., Klaerke, D. A., Loo, D. D. F., Wright, E. M., and Zeuthen, T. 1998. The human Na+-glucose cotransporter is a molecular water pump. J. Physiol. 508: 15–21.
Google Scholar
Ma cA ulay, N., Gether, U., Klaerke, D. A., and Zeuthen, T. 2001. Water transport by the human Na+-coupled glutamate cotransporter expressed in Xenopus oocytes. J. Physiol. 530:367–378.
Google Scholar
Zeuthen, T. 2000 Molecular water pumps. Rev. Physiol. Biochem. Pharmacol. 141:97–151.
Google Scholar
Zeuthen, T. 2002. General models for water transport across leaky epithelia. Int. Rev. Cytol. 215:285–317.
Google Scholar
Zeuthen, T., Meinild, A.-K., Loo, D. D. F., Wright, E. M., and Klaerke, D. A. 2001. Isotonic transport by the Na+-glucose cotransporter SGLT1 from humans and rabbit. J. Physiol. 531: 631–644.
Google Scholar
Zeuthen, T. and Ma cA ulay, N. 2002. Cotransporters as molecular water pumps. Int. Rev. Cytol. 215:259–284.
Google Scholar
Nissenson, A. R., Levin, M. L., Klawans, H. L., and Nausieda, P. L. 1977. Neurological sequelae of end stage renal disease (ESRD). J. Chron. Dis. 30: 705–733.
Google Scholar
Wells, T. 1998. Vesicular osmometers, vasopressin secretion and aquaporin-4: A new mechanism for osmoreception? Mol. and Cell. Endocrinol. 136:103–107.
Google Scholar
Neely, J. D., Christensen, B. M., Nielsen, S., and Agre, P. 1999. Heterotetrameric composition of aquaporin-4 water channels. Biochemistry 38:11156–11163.
Google Scholar
Nicchia, G. P., Frigerl, A., Liuzzi, G. M., Santacroce, M. P., Nico, B., Procino, G., Quondamatteo, F., Herken, R., Roncali, L., and Svelto, M. 2000. Aquaporin-4-containing astrocytes sustain a temperature-and mercury-insensitive swelling in vitro. Glia 31:29–38.
Google Scholar
Niermann, H., Amiry-Moghaddam, M., Holthoff, K., Witte, O. W., and Ottersen, O. P. 2001. A novel role of vasopressin in the brain: Modulation of activity-dependent water flux in the neocortex. J. Neurosci. 21:3045–3051.
Google Scholar
Zhu, X.-H. and Chen, W. 2001. Observed BOLD effects on cerebral metabolite resonances in human visual cortex during visual stimulation: A functional 1H MRS study at 4 T. Magn. Reson. Med. 46:841–847.
Google Scholar
Mayeux, V., Pons, F., Baldy-Moulinier, M., and Valmier, J. 1996. Early postnatal muscle contractile activity regulates the carbonic anhydrase phenotype of proprioceptive neurons in young and mature mice: Evidence for a critical period in development. Neuroscience 71:787–795.
Google Scholar
Cammer, W., Zhang, H., and Cammer, M. 1993. Glial cell abnormalities in the CNS of the carbonic anhydrase II deficient mutant mouse. J. Neurolog. Sci. 118:1–9.
Google Scholar
Sapirstein, V. S., Durrie, R., Nolan, C. E., and Marks, N. 1993. Identification of membrane-bound carbonic anhydrase in white matter coated vesicles: The fate of carbonic anhydrase and other white matter coated vesicle proteins in triethyl tin-induced leukoencephalopathy. J. Neurosci. Res. 35:83–91.
Google Scholar
Fischer, I., Durrie, R., and Sapirstein, V. S. 1994. Plasmolipin: The other myelin proteolipid—A review of studies of its structure, expression, and function. Neurochem. Res. 19:959–966.
Google Scholar
Thiel, T., Ensenauer, R., Lehnert, W., Hennig, J., and Martin, E. 2001. Detection and monitoring of neurometabolic diseases using in vivo magnetic resonance spectroscopy. Neurochem. News Newslett. 1:125–128.
Google Scholar