Astrocyte-neuron interaction during one-trial aversive learning in the neonate chick

Neuroscience and Biobehavioral Reviews

Volumn 20, Issue 3, 1996, Pages 537-551

  Hertz, Leif ^a   Gibbs, Marie E ^b   O'Dowd, Brona S ^b   Sedman, Garry L ^b   Robinson, Stephen R ^c   Syková, Eva ^d   Hajek, Ivan ^d   Heritz, Elna ^a   Liang, Peng ^a   Rong, Huang ^a   Kim, T Ng ^b  

^a UNIVERSITY OF SASKATCHEWAN   (Canada)

^b LA TROBE UNIVERSITY   (Australia)

^c INSTITUTE OF EXPERIMENTAL MEDICINE   (Czech Republic)

^d NONE

Author keywords

Astrocyte; Energy metabolism; Fluoroacetate; Glial cell; Glutamate; Glutamine; Glycogen; Glycolysis; Learning; Memory; Methionine sulfoximine; Neuropil; Noradrenaline; Potassium ion

Indexed keywords

ASTROCYTE; AVERSIVE BEHAVIOR; CELL INTERACTION; CHICKEN; GLIA CELL; GLYCOLYSIS; LEARNING; MEMORY; NONHUMAN; PRIORITY JOURNAL; REVIEW;

EID: 0029810057     PISSN: 01497634     EISSN: None     Source Type: Journal    
DOI: 10.1016/0149-7634(95)00020-8     Document Type: Article

References (96)

1. Albers, B.; Bray, D.; Lewis, J.; Raff, M.; Roberts, K.; Watson, J. D. Molecular biology of the cell, 2nd edn. New York: Garland Publishing; 1989.
2. Barres B.A. New roles for glia. J. Neurosci. 11:1991;3684-3695.
3. Benveniste H., Drejer J., Schousboe A., Diemer N.H. Elevation of the extracellular concentrations of glutamate and aspartate in rat hippocampus during transient cerebral ischemia monitored by intracranial microdialysis. J. Neurochem. 43:1984;1369-1374.
4. Chen Y., McNeill J.R., Hajek I., Hertz L. Effect of vasopressin on brain swelling at the cellular level - Do astrocytes exhibit a furosemide-vasopressin-sensitive mechanism for volume regulation? Can. J. Physiol. Pharmacol. 70:1992;S219-S222.
5. IC receptor in glia cells. Brain Res. Bull. 38:1995;153-159.
6. Cornell-Bell A.H., Finkbeiner S.M., Cooper M.S., Smith S.J. Glutamate induces calcium waves in cultured astrocytes: Long-range glial signalling. Science. 247:1990;470-473.
7. Crowe S.F., Ng K.T., Gibbs M.E. Forebrain noradrenaline concentration following weakly reinforced training. Pharmacol. Biochem. Behav. 40:1991;173-176.
8. Cserr H.F., Bundgaard M. The neural microenvironment: A comparative view. Ann. N.Y. Acad. Sci. 481:1986;1-6.
9. 14C] lactate into the glycogen of cultured mouse astroglial cells. Evidence for gluconeogenesis in brain cells. Biol. Chem. Hoppe Sayler. 374:1993;343-347.
10. Engelsen B., Fonnum F. The effect of methionine sulfoximine, an inhibitor of glutamine synthetase, on the levels of amino acids in the intact and decorticated rat neostriatum. Brain Res. 388:1985;165-168.
11. Gibbs M.E. Behavioural and pharmacological unravelling of memory formation. Neurochem. Res. 16:1991;715-736.
12. Gibbs M.E., Ng K.T. Psychobiology of memory: Towards a model of memory formation. Biobehav. Rev. 1:1977;113-136.
13. Gibbs, M.E.; O'Dowd, B.S.; Hertz, L.; Robinson, S.R.; Sedman, G.L.; Ng, K.T. Inhibition of glutamine synthetase activity prevents memory consolidation. Brain Res. in press.
14. Grab D., Reisert I., Pilgrim C. Volumendichte und spezifische Oberflächen neuronaler und glioser Gewebselemente in verschiedenen Regionen des Rattenhirns. Verhandl. Anat. Gesellsch. 77:1983;255-256.
15. +-ATPase (EC 3.6.1.3) of bulk isolated glial cells, perikarya and synaptosomes from rabbit brain cortex. Brain Res. 165:1979;87-103.
16. +-ATPase activity in cultured mouse neurons and astrocytes. Neurochem. Int. in press.
17. +-ATPase activity in young chicks after taste stimulation. Brain Res. Bull. 33:1994;87-91.
18. Hamprecht, B. Energy metabolism. In: Kettenmann, H.; Ransom, B., eds. Glial cells. in press.
19. Hansson E., Ronnback L. Regulation of glutamate and GABA transport by adrenoceptors in primary astroglial cell cultures. Life Sci. 44:1988;27-34.
20. Hassel B., Sonnewald U., Unsgard G., Fonnum F. NMR spectroscopy of cultured astrocytes: Effects of glutamine and the gliotoxin fluorocitrate. J. Neurochem. 62:1994;2187-2194.
21. Henn, F.A. Separation of neuronal and glial cells and subcellular constituents. In: Fedoroff, S.; Hertz, L., eds. Advances in cellular neurobiology, vol. 1. New York: Academic Press; 1980:373-403.
22. + concentration. Brain Res. 43:1972;437-443.
23. Herreras O., Somjen G.G. Propagation of spreading depression among dendrites and somata of the same cell population. Brain Res. 610:1993;276-282.
24. + in hippocampus of anesthetized rats. Brain Res. 610:1993;283-294.
25. Hertz L. Is Alzheimer's disease an anterograde degeneration, originating in the brainstem, and disrupting metabolic interactions between neurons and glial cells? Brain Res. Rev. 14:1989;335-353.
26. Hertz L. Autonomic control of neuronal-astrocytic interactions, regulating metabolic activities and ion fluxes in the CNS. Brain Res. Bull. 29:1992;303-313.
27. Hertz L., Drejer J., Schousboe A. Energy metabolism in glutamatergic neurons, GABAergic neurons and astrocytes in primary culture. Neurochem. Res. 13:1988;605-610.
28. Hertz, L.; Hertz, T. Neuronal-glial interactions. In: Bittar, E.E.; Bittar, N., eds. Principles of medical biology. Greenwich: JAI Press. in press.
29. Hertz, L.; O'Dowd, B.; Ocherashvili, E. Glial cells. In: Ramachandran, V. S., ed. Encyclopedia of human behavior, vol. 2. Orlando, FL: Academic Press; 1994:429-439.
30. Hertz L., Peng L. Effects of monoamine transmitters on neurons and astrocytes: Correlation between energy metabolism and intracellular messengers. Prog. Brain Res. 93:1992;283-301.
31. Hertz L., Peng L., Hertz E., Juurlink B.H.J., Yu P.H. Development of monoamine axidase activity and monoamine effects on glutamate release in cerebellar neurons and astrocytes. Neurochem. Res. 10:1989;1039-1096.
32. Hertz, L.; Peng, L.; Westergaard, N.; Yudkoff, M.; Schousboe, A. Neuronal-astrocytic interactions in metabolism of transmitter amino acids of the glutamate family. In: Schousboe, A.; Diemer, N. N.; Kofod, H., eds. Drug research related to neuroactive amino acids. Copenhagen: Munksgaard, 1992:30-50.
33. Hoffmann E.K. Introduction III: Cell swelling and volume regulation. Can. J. Physiol. Pharmacol. 70:1992;S310-S313.
34. Huang R., Peng L., Chen Y., Hajek I., Zhao S., Hertz L. Signalling effect of elevated potassium concentrations and monoamines on brain energy metabolism at the cellular level. Dev. Neurosci. 16:1994;1-15.
35. Huang R., Shuaib A., Hertz L. Glutamate uptake and glutamate content in primary cultures of mouse astrocytes during anoxia, substrate deprivation and simulated ischemia under normothermic and hypothermic conditions. Brain Res. 618:1993;346-351.
36. Huguenard J.R., Hamill O.P., Prince D.A. Sodium channels in dendrites of rat cortical pyramidal neurons. Proc. Natl Acad. Sci. U.S.A. 86:1989;2475-2477.
37. Hyden H. Behavior, neural function and RNA. Prog. Nucl. Acid. Res. 6:1967;187-218.
38. + channel in glioma cells but not neuroblastoma cells in culture. Biochem. Biophys. Res. Commun. 109:1982;100-105.
39. Kadekaro M., Crane A.M., Sokoloff L. Differential effects of electrical stimulation of sciatic nerve on metabolic activity in spinal cord and dorsal root ganglion in the rat. Proc. Natl Acad. Sci. U.S.A. 82:1985;6010-6013.
40. Kaufman E.E., Driscoll B.F. Carbon dioxide fixation in neuronal and astroglial cells in culture. J. Neurochem. 58:1992;258-262.
41. Kauppinen R.A., Enkvist K., Holopainen I., Akerman K.E. Glucose deprivation depolarizes plasma membrane of cultured astrocytes and collapses transmembrane potassium and glutamate gradients. Neuroscience. 26:1988;283-289.
42. Keyser D.O., Pelmar T.C. Synaptic transmission in the hippocampus: Critical role for glial cells. Glia. 10:1994;237-243.
43. Kimelberg, H.K., ed. Glial cell receptors. New York: Raven Press; 1988.
44. Laming P.R. Do glia contribute to behaviour? A neuromodulatory review. Comp. Biochem. Physiol. 94A:1989;555-568.
45. Lee K.M., Rosa M.G.P., Schmid L.M., Robinson S.R. Ocular dominance shifts in cat visual cortex following selective blockade of glial glutamine in the retina. Proc. Austr. Neurosci. Soc. 5:1994;165.
46. 2 presynaptic receptors mediate inhibition of glutamate release from cerebellar mossy fibre terminals. Eur. J. Pharmacol. 202:1991;185-190.
47. +-ATPase in the rat brain. Neurochem. Int. 21:1992;119-127.
48. Murphy S., Pearce B. Functional receptors for neurotransmitters on glial cells. Neurosci. 22:1987;381-394.
49. Ng, K.T.; Gibbs, M.E. Stages of memory formation: A review. In: Andrew, R. J., ed. Neural and behavioural plasticity: The use of the domestic chick as a model. Oxford: Oxford University Press; 1991:351-269.
50. Ng K.T., Gibbs M.E., Crowe S.F., Sedman G.L., Hua F., Zhao W., O'Dowd B., Rickard N., Gibbs C.L., Sykov E., Svoboda J., Jendelova P. Molecular mechanisms of memory formation. Mol. Neurobiol. 5:1992;333-350.
51. Ng K.T., Gibbs M.E., Gibbs C.L., Sedman G., Svoboda J., Jendelova P., O'Dowd B., Rickard N., Crowe S.F. Ion involvement in memory formation: The potential role of astrocytes. Prog. Brain Res. 94:1992;109-115.
52. Ng, K.T.; Rickard, N.S.; O'Dowd, B.S.; Zhao, W.-Q.; Gibbs, M.E.; Sedman, G.L.; Robinson, S.R.; Hertz, L. Complex roles of glutamate in the Gibbs-Ng model of one-trial aversive learning in the new-born chick. Brain Res. Bull.; in press.
53. Norenberg M.D., Martinez-Hernandez A. Fine structural localization of glutamine synthetase in astrocytes of rat brain. Brain Res. 161:1979;303-310.
54. O'Dowd, B.S. Metabolic activity in astrocytes essential for the consolidation of one-trial passive avoidance memory in the day-old chick. Ph.D. Thesis, La Trobe University; 1995.
55. O'Dowd B.S., Barrington J., Ng K.T., Hertz E., Hertz L. Glycogenolytic response of primary chick and mouse cultures of astrocytes to noradrenaline across development. Dev. Brain Res. 88:1995;220-223.
56. O'Dowd B.S., Gibbs M.E., Ng K.T., Hertz E., Hertz L. Astrocytic glycogenolysis energizes memory processes in neonate chicks. Dev. Brain Res. 78:1994;137-141.
57. O'Dowd B.S., Gibbs M.E., Sedman G.L., Ng K.T. Astrocytes implicated in the energizing of intermediate memory processes in neonate chicks. Cogn. Brain Res. 2:1994;93-102.
58. O'Grady S.M., Palfrey H.C., Field M. Characteristics and functions of Na-K-Cl cotransport in epithelial tissues. Cell Physiol. 22:1987;C177-C192.
59. Palay, S.L.; Chan-Palay, V. Cerebellar cortex: Cytology and organization. New York: Springer; 1974.
60. Peng, L. Metabolic trafficking between neurons and astrocytes. Ph.D. Thesis, University of Saskatchewan; 1994.
61. Peng L., Hertz L. Potassium-induced stimulation of oxidative metabolism of glucose in cultures of normal cerebellar granule cells but not in corresponding cells with dendritic degeneration. Brain Res. 629:1993;331-334.
62. Peng L.A., Schousboe A., Hertz L. Utilization of alpha-ketoglutarate as a precursor for transmitter glutamate in cultured cerebellar granule cells. Neurochem. Res. 16:1991;29-34.
63. + concentration stimulates oxidative metabolism in a glutamatergic neuronal culture and glycolysis in cultured astrocytes but has little effect in a GABAergic neuronal culture. Brain Res. 63:1994;168-172.
64. Peters, A.; Palay, S.L.; Webster, H. deF. The fine structure of the nervous system. Neurons and their supporting cells, 3rd edn. New York: Oxford University Press; 1991:1-494.
65. Pope, A. Neuroglia: Quantitative aspects. In: Schoffeniels, E.; Franck, G.; Hertz, L., Tower, D.B., eds. Dynamic properties of glia cells. Oxford: Pergamon Press; 1978:13-20.
66. Pow D.V., Robinson S.R. Glutamate in some retinal neurons is derived solely from glia. J. Neurosci. 60:1994;355-366.
67. Rauen T., Jeserich G., Danbolt N.G., Kanner B.I. Comparative analysis of sodium-dependent L-glutamate transport of synaptosomal and astroglial membrane vesicles from mouse cortex. FEBS Lett. 312:1992;15-20.
68. Rickard, N.S. Glutamate receptor-mediated processing in memory consolidation in the day-old chick. Ph.D. Thesis, LaTrobe University; 1995.
69. Rickard N.S., Poot A.C., Gibbs M.E., Ng K.T. Both non-MNDA and NMDA glutamate receptors are necessary for memory consolidation in the day-old chick. Behav. Neurol. Biol. 62:1994;33-40.
70. Roitbak, A.I. Glia and its role in nervous activity (in Russian). Moscow: Nauka; 1993:1-392.
71. Rosenthal K., Sick T.J. Glycolytic and oxidative metabolic contributions to potassium ion transport in rat cerebral cortex. Can. J. Physiol. Pharmacol. 70:1992;165-169.
72. Schousboe A., Westergaard N., Sonnewald U., Petersen S.B., Yu A.C.H., Hertz L. Regulatory role of astrocytes for neuronal biosynthesis and homeostasis of glutamate and GABA. Prog. Brain Res. 94:1992;199-212.
73. Sedman G., O'Dowd B., Rickard N., Gibbs M.E., Ng K.T. Brain metabolic activity associated with long-term memory consolidation. Mol. Neurobiol. 5:1992;351-354.
74. Smith S.J. Do astrocytes process neural information? Prog. Brain Res. 94:1992;119-136.
75. Sochocka E., Juurlink B.H., Code W.E., Hertz V., Peng L., Hertz L. Cell death in primary cultures of mouse neurons and astrocytes during exposure to and `recovery' from hypoxia, substrate deprivation and simulated ischemia. Brain Res. 638:1994;21-28.
76. Sokoloff, L. The brain as a chemical machine. In: Yu, A.C.H.; Hertz, L.; Norenberg, M.D.; Sykova, E.; Waxman, S.G., eds. Progress in brain research, vol. 94. Amsterdam: Elsevier, 1992:19-33.
77. 13C-glucose metabolism in neocortical astrocytes: Evidence for mitochondrial heterogeneity. Dev. Neurosci. 15:1993;351-357.
78. Sorg O., Magistretti P.J. Characterisation of the glycogenolysis elicited by vasoactive intestinal peptide, noradrenaline and adenosine in cultures of mouse cerebral cortex astrocytes. Brain Res. 563:1991;227-233.
79. Stone E.A., Ariano M.A. Are glial cells targets of the central noradrenergic system? A review of the evidence. Brain Res. 14:1989;297-309.
80. Stuart G.J., Sakmann B. Active propagation of somatic action potentials into neocortical pyramidal cell dendrites. Nature. 367:1994;69-72.
81. Subbarao K.V., Hertz L. Effects of adrenergic agonists on glycogenolysis in primary cultures of astrocytes. Brain Res. 536:1990;220-226.
82. Swanson R.A., Graham S.H. Fluorocitrate and fluoroacetate effects on astrocyte metabolism in vitro. Brain Res. 664:1994;94-100.
83. Sweadner K.J. Overlapping and diverse distribution of Na-K ATPase isozymes in neurons and glia. Can. J. Physiol. Pharmacol. 70:1992;S255-S259.
84. +-ATPase. In: Kettenmann, H.; Ransom, B., eds. Glial cells. In press.
85. + accumulation in the central nervous system. Prog. Biophys. Mol. Biol. 42:1983;135-189.
86. Syková, E. Ionic and volume changes in the microenvironment of nerve and receptor cells. In: Autrum, H.; Ottoson, D.; Perl, E. R.; Schmidt, R. F.; Shimazu, H.; Willis, W. D., eds. Progress in sensory physiology, vol. 13. New York: Springer; 1992:1-162.
87. Syková E., Jendelova P., Svoboda J., Sedman G., Ng K.T. Activity-related rise in extracellular potassium concentration in the brain of 1-3-day-old chicks. Brain Res. Bull. 24:1990;569-575.
88. Walz W. Role of Na/K/Cl cotransport in astrocytes. Can. J. Physiol. Pharmacol. 70:1992;S260-S262.
89. Walz W., Hertz L. Functional interactions between neurons and astrocytes. II. Potassium homeostasis at the cellular level. Prog. Neurobiol. 20:1983;133-183.
90. Westergaard N., Sonnewald U., Schousboe A. Release of α-KG, malate and succinate from cultured astrocytes: Possible role in amino acid neurotransmitter homeostasis. Neurosci. Lett. 176:1994;105-109.
91. Westergaard N., Varming T., Peng L., Sonnewald U., Hertz L., Schousboe A. Uptake, release, and metabolism of alanine in neurons and astrocytes in primary cultures. J. Neurosci. Res. 35:1993;540-545.
92. White H.S., Chow S.Y.C., Yen-Chow Y.C., Woodbury D.M. Effects of potassium on the ion content of mouse astrocytes and neurons. Can. J. Physiol. Pharmacol. 70:1992;S263-S268.
93. Wolff, J.R. Quantitative aspects of astroglia. VIth Int. Congress Neuropathol. 727-733; 1970.
94. Yudkoff M., Nissim I., Hertz L., Pleasure D., Erecinska M. Nitrogen metabolism: Neuronal-astroglial relationships. Prog. Brain Res. 94:1992;213-224.
95. Zetterstrom T., Vernet L., Ungerstedt U., Tossman U., Johzom B., Fredholm B.B. Purine levels in the intact rat brain. Studies with an implanted perfused hollow fibre. Neurosci. Lett. 29:1982;111-115.
96. Zhao W.-Q., Ng K.T., Sedman G.L. Passive avoidance learning induced change in GAP43 phosphorylation in day-old chicks. Brain Res. Bull. 36:1994;11-17.