Abstract
The lactate accumulated during late gestation is actively oxidized within the first hours of extrauterine life (Medina et al., 1980; Persson and Tunell, 1971), indicating that neonatal tissues actively utilize blood lactate. It is noteworthy that gluconeogenesis is not yet induced in these circumstances (Fernandez et al., 1983; Medina et al., 1980), in agreement with the idea that lactate is utilized directly as a source of energy and carbon skeletons by some neonatal tissues (see: Medina et al., 1992). Since lactate removal takes place at a very high rate, it is likely that several tissues would be involved in lactate utilization. Thus, it has been reported that neonatal lung (Patterson et al., 1986), heart (Fernandez, E. and Medina, J. M., unpublished results), and liver (Almeida et al., 1992) utilize lactate for energy production and/or lipogenic purposes. However, special attention has been paid to lactate utilization by the brain, probably because this organ must continue its development even under the starvation that occurs during the presuckling period. Lactate utilization by the brain has been reported in fetal (Bolanos and Medina, 1993), early newborn (Arizmendi and Medina, 1983; Fernández and Medina, 1986; Vicario et al., 1991; Vicario and Medina, 1992) and suckling rats (Dombrowski et al., 1989; Itoh and Quastel, 1970), in newborn dogs (Hellmann et al., 1982) and in glucose-6-phosphatase-deficient human babies (Fernandes et al., 1984).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Almeida, A., Bolanos, J.P., and Medina, J.M. (1992) Ketogenesis from lactate in rat liver during the perinatal period. Pediatr. Res. 31: 415–418.
Amoroso, S., Schmid-Antomarchi, H., Fosset, M., and Lazdunski, M. (1990) Glucose, sulfonylureas, and neurotransmitter release: role of ATP-sensitive K+ channels. Science 247: 852–854.
Arizmendi, C. and Medina, J.M. (1983) Lactate as an oxidizable sustrate for rat brain in vivo during perinatal period. Biochem. J. 214: 633–635.
Bell, J.E., Hume, R., Busuttil, A., and Burchell, A. (1993) Immunocytochemical detection of the microsomal glucose-6-phosphate in human brain astrocytes. Neuropathol Appl. Neurobiol 19: 429–435.
Bennett, M.V.L. (1977) Electrical transmission: a functional analysis and comparison with chemical transmission. In:Cellular biology of neurons, Handbook of Physiology, The nervous system. E. Kandel, ed., Williams and Wilkins, Baltimore, Vol. 1, pp. 357–416.
Bennett, M.V.L., Barrio, T.A., Bargiello, T.A., Spray, D.C., Hertzberg, E., and Sáez, J.C. (1991) Gap junctions: new tools, new answers, new questions. Neuron 6: 305–32
Bock, A., Tegtmeier, F., Hansen, A., and Holler, M. (1993) Lactate and postischemic recovery of energy metabolism and electrical activity in the isolated perfused rat brain. J. Neurosurg. Anesthesiol. 5: 94–10
Bolanos, J.P. and Medina, J.M. (1993) Lipogenesis from lactate in fetal rat brain during late gestation. Pediatr. Res. 33: 66–71.
Brookes, N. and Yarowssy, P.J. (1985) Determinants of deoxyglucose uptake in cultured astrocytes: the role of the sodium pump. J. Neurochem. 44: 473–479.
Bruzzone, R., White, T.W., and Paul, D.L. (1996) Connections with connexins: The molecular basis of direct intercellular signalling. Europ. J. Biochem. (in press).
Cremer, J.E. (1982) Substrate utilization and brain development. J. Cer. Blood Flow Metab. 2: 394–407.
Dombrowski, G.J., Swiatek, K.R., and Chao, K.L. (1989) Lactate, 3-hydroxybutyrate and glucose as substrates for the early postnatal rat brain. Neurochem Res 14: 667–675.
Dringen, R., Gebhardt, R., and Hamprecht, B. (1993) Glycogen in astrocytes, possible function as lactate supply for neighboring cells. Brain Res. 62: 208–214.
El-Fouly, M.H., Trosko, J.E., and Chang, C.-C. (1987) A rapid and simple technique to study gap junctional intercellular communication. Exp. Cell Res.\168: 422–430.
Enkvist, M.O.K. and McCarthy, K.D. (1994) Astroglial gap junction communication is increased by treatment with either glutamate or high K+ concentration. J. Neurochem. 62: 489–495.
Fernandes, J., Berger, R., and Smit, G.P.A. (1984) Lactate as a cerebral metabolic fuel for glucose-6-phosphate deficient children. Pediatr. Res. 18: 335–339.
Fernández, E. and Medina, J.M. (1986) Lactate utilization by the neonatal rat brain in vitro. Competition with glucose and 3-hydroxybutyrate. Biochem. J. 234: 489–492.
Fernández, E., Valcarce, C, Cuezva, J.M., and Medina, J.M. (1983) Postnatal hypoglycæmia and gluconeogenesis in the newborn rat. Delayed onset of gluconeogenesis in prematurely delivered newborns. Biochem. J. 214: 525–532.
Fuxe, K., Tinner, B., Staines, W., Hemsen, A., Hersh, L., and Lundberg, J. (1991) Demonstration and nature of endothelin-3-like immunoreactivity in somatostatin and choline acetyltransferase-immunoreactive nerve cells of the neostriatum of the rat. Neurosci. Lett. 123: 107–111.
Giaume, C., Cordier, J., and Glowinski, X (1992) Endothelins inhibit junctional permeability in cultured mouse astrocytes. Eur. J. Neurosc. 4: 877–881.
Giaume, C., Marin, P., Cordier, J., Glowinski, J., and Premont, J. (1991) Adrenergic regulation of intercellular communications between cultured striatal astrocytes from the mouse. Proc. Natl. Acad. Sci. USA 88: 5577–5581.
Giaume, C. and McCarthy, K.D. (1996) Control of gap-junctional communication in astrocytic networks. T.I.N.S. 19: 319–325.
Giaume, C., Tabernero, A., and Medina, J.M. (1997) Metabolic trafficking through astrocytic gap junctions. Glia 21: 114–123.
Granda, B., Tabernero, A., Sánchez-Abarca, L.I., and Medina, J.M. (1998) The K-ATP channel regulates the effect of Ca2+ on gap junction permeability in cultured astrocytes. FEBS Letters En prensa.
Hellmann, J., Vanucci, R.C., and Nardis, E. (1982) Blood-brain barrier permeability to lactic acid in the newborn dog: lactate as a cerebral metabolic fuel. Pediatr. Res. 16: 40–44.
Itoh, T. and Quastel, J.H. (1970) Acetoacetate metabolism in infant and adult rat brain in vitro. Biochem. J. 116: 641–655.
Izumi, Y., Benz, A., Zorumski, G, and Olney, J. (1994) Effects of lactate and pyruvate on glucose deprivation in rat hippocampal slices. Neuroreport 5: 617–620.
Kawai, N., Yamamoto, T, Yamamoto, H., Mc Carron, R.M., and Spatz, M. (1994) Endothelin stimulates ATPase activity in brain capillary endothelium. J. Physiol. 480: P17–P17.
Klaunig, J.E. and Ruch, R.J. (1990) Role of inhibition of intercellular communication in carcinogenesis. Lab. Invest. 62: 135–146.
Lavado, E., Sanchez-Abarca, L.I., Tabernero, A., Bolaños, J.P., and Medina, J.M. (1997) Oleic acid inhibits gap junction permeability and increases glucose uptake in cultured rat astrocytes. J. Neurochem. 69: 721–728.
Loewenstein, W. (1981) Junctional intercellular communication: the cell-to-cell membrane channel. Physiol. Rev. 61: 829–913.
Mac Cumber, M.W., Ross, C.A., and Snyder, S.H. (1990) Endothelin in brain: receptors, mitogenesis and biosynthesis in glial cells. Proc. Natl. Acad. Sei. USA 87: 2359–2363.
Maran, A., Cranston, I., Lomas, J., Macdonald, I., and Amiel, S. (1994) Protection by lactate of cerebral function during hypoglycaemia. Lancet 343: 16–20.
Medina, J.M., Cuezva, J.M., and Mayor, F. (1980) Non-gluconeogenic fate of lactate during the early neonatal period in the rat. FEBS Lett. 114: 132–134.
Medina, J.M., Vicario, C., Juanes, M., and Fernández, E. (1992) R. Knopp, ed., CRC Press, Boca Raton, FL, Vol. pp. 233–258
Naus, C.C.G, Bechberger, J.F, Caveney, S., and Wilson, J.X. (1991) Expression of gap junction genes in astrocytes and C6 glioma cells. Neurosci. Lett. 126: 33–36.
Neyton, J. and Trautman, A. (1985) Single-channel currents of an intercellular junction. Nature 317: 331–335.
Nicolino, M. (1997) Hyperinsulinisme du nourrisson: le roôle-cle des canaux K+. Med. Sci. 13: 276–277.
Niki, I. and Ashcroft, S.J. (1993) Characterization and solubilization of the sulphonylurea receptor in rat brain. Neuropharmacology 32: 951–957.
Patterson, C.E., Konini, M.V., Selig, W.M., Owens, C.M., and Rohades, R. (1986) Integrated substrate utilization by perinatal lung. Exp. Lung Res. 10: 71–86.
Pellerin, L. and Magistretti, P. (1994) Glutamate uptake into astrocytes stimulates aerobic glycolysis: a mechanism coupling neuronal activity to glucose utilization. Proc. Natl. Acad. Sei. USA 91: 10625–10629.
Peracchia, C., Lazrak, A., and Peracchia, L.L. (1994) Molecular models of channel interaction and gating in gap junctions. In: Handbook of membrane channels. C Peracchia, ed., Academic Press, Vol. pp. 361–377.
Persson, B. and Tunell, R. (1971) Influence of environmental temperature and acidosis on lipid mobilization in the human infant during the first two hours after birth. Acta Pædiatr. Scand. 60: 385–398.
Rose, C.R. and Ransom, B.R. (1997) Gap junction equalize intracellular Na+ concentration in astrocytes. Glia 20: 299–307.
Schousboe, A., Westergaard, N., and Hertz, L. (1993) Neuronal-Astrocytic Interactions in Glutamate Metabolism. Biochem. Soc. Trans. 21: 49–53.
Schurr, A., West, C.A., and Rigor, B.M. (1988) Lactate-supported synaptic function in the rat hippocampal slice preparation. Science 240: 1326–1328.
Sonnewald, U., Westergaard, N., Krane, J., Unsgard, G., Petersen, S.B., and Schousboe, A. (1991) First direct demonstration of preferential release of citrate from astrocytes using <C-13> NMR spectroscopy of cultured neurons and astrocytes. Neurosci. Lett. 128: 235–239.
Tabernero, A., Bolanos, J.P., and Medina, J.M. (1993) Lipogenesis from lactate in rat neurons and astrocytes in primary culture. Biochem. J. 294: 635–638.
Tabernero, A., Giaume, C., and Medina, J.M. (1996a) Endothelin-1 regulates glucose utilization in cultured rat astrocytes by controlling intercellular communication through gap junctions. Glia 16: 187–195.
Tabernero, A., Vicario, C, and Medina, J.M. (1996b) Lactate spares glucose as a metabolic fuel in neurons and astrocytes from primary culture. Neurosci. Res. 26: 369–376.
Takahashi, S., Driscoll, F., Law, M.J., and Sokoloff, L. (1995) Role of sodium and potasium ions in regulation of glucose metabolism in cultured astroglia. Proc. Natl. Acad. Sci. USA 92: 4616–4620.
Venance, L., Stella, N., Glowinski, I, and Giaume, C. (1997) Mechanism involved in initiation and propagation of receptor-induced intercellular calcium signalling in cultured rat astrocytes. J. Neurosci. 17: 1981–1992.
Vera, B., Sanchez-Abarca, L.I., Bolanos, J.R, and Medina, J.M. (1996) Inhibition of astrocyte gap junctional communication by ATP depletion is reversed by calcium sequestration. FEBS letters 392: 225–228.
Vicario, C., Arizmendi, C., Malloch, J.G., Clark, J.B., and Medina, J.M. (1991) Lactate utilization by isolated cells from early neonatal rat brain. J. Neurochem. 57: 1700–1707.
Vicario, C. and Medina, J.M. (1992) Metabolism of lactate in the rat brain during the early neonatal period. J. Neurochem. 58: 32–40.
Vicario, C., Tabernero, A., and Medina, J.M. (1993) Regulation of lactate metabolism by albumin in rat neurons and astrocytes from primary culture. Pediatr. Res. 34: 709–715.
Virsolvy-Vergine, A., Salazar, G., Sillard, R., Denoroy, L., Mutt, V., and Bataille, D. (1996) Endosulfine, endogenous ligand for the sulphonylurea receptor. Diabetologia 39: 135–141.
Westergaard, N., Sonnewald, U., and Schousboe, A. (1994) Release of alpha-ketoglutarate, malate, and succinate from cultured astrocytes: possible role in amino acid neurotransmitter homeostasis. Neurosci. Lett. 176: 105–109.
Xia, Y., Eisenman, D., and Haddad, G.G. (1993) Sulphonylurea receptor in rat brain: effect of chronic hypoxia during development. Pediatr. Res. 34: 634–641.
Yoshimoto, S., Ishizaki, Y., Kurihara, H., Sasaki, T, Yoshizumi, M., Yanagisawa, M., Yazaki, Y., Masaki, T., Takakura, K., and Murota-S (1990) Cerebral microvessel endothelium is producing endothelin. Brain. Res. 508: 283–285.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1999 Springer Science+Business Media New York
About this chapter
Cite this chapter
Medina, J.M., Tabernero, A., Giaume, C. (1999). Metabolic Coupling and the Role Played By Astrocytes in Energy Distribution and Homeostasis. In: Matsas, R., Tsacopoulos, M. (eds) The Functional Roles of Glial Cells in Health and Disease. Advances in Experimental Medicine and Biology, vol 468. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-4685-6_28
Download citation
DOI: https://doi.org/10.1007/978-1-4615-4685-6_28
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4613-7121-2
Online ISBN: 978-1-4615-4685-6
eBook Packages: Springer Book Archive