Modulation of AMPA receptor subunits GluR1 and GluR2/3 in the rat cerebellum in an experimental hepatic encephalopathy model

Brain Research

Volumn 778, Issue 2, 1997, Pages 346-353

  Suarez I ^a   Bodega, G ^a   Fernandez B ^b  

^a UNIVERSITY OF ALCALÁ   (Spain)

^b UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

Author keywords

AMPA receptor; Bergmann glial cell; Portocaval anastomosis; Purkinje neuron

Indexed keywords

AMPA RECEPTOR;

ANIMAL MODEL; ARTICLE; CELL INTERACTION; CEREBELLUM; HEPATIC ENCEPHALOPATHY; IMMUNOREACTIVITY; NONHUMAN; PATHOPHYSIOLOGY; PORTOCAVAL SHUNT; PRIORITY JOURNAL; PURKINJE CELL; RAT;

ANIMALS; DISEASE MODELS, ANIMAL; GLUTAMIC ACID; HEPATIC ENCEPHALOPATHY; IMMUNOHISTOCHEMISTRY; MALE; NEUROGLIA; PORTACAVAL SHUNT, SURGICAL; PURKINJE CELLS; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, AMPA;

EID: 0031578874     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(97)01089-5     Document Type: Article

References (62)

1. Attwell D., Barbour B., Szathowski M. Nonvesicular release of neurotransmitter. Neuron. 11:1993;401-407.
2. Baude A., Nusser Z., Latawiec D., McIlhinney R.A.J., Somogyi P. Synaptic and nonsynaptic localization of the GluR1 subunit of the AMPA-type excitatory amino acid receptor in the rat cerebellum. J. Neurosci. 14:1994;2830-2843.
3. Bergmann M., Fox P.A., Grabs D., Post A., Schilling K. Expression and subcellular distribution of glutamate receptor subunits 2/3 in the developing cerebellar cortex. J. Neurosci. Res. 43:1996;78-86.
4. Bodega G., Suárez I., Arilla E., Rubio M., Fernández B. Heterogeneous astroglial response in the rat spinal cord to long-term portacaval shunt. An immunohistochemical study. Glia. 4:1991;400-407.
5. Butterworth R.F., Le O., Lavoie J., Szerb J.C. Effect of portacaval anastomosis on electrically stimulated release of glutamate from rat hippocampal slices. J. Neurochem. 56:1991;1481-1484.
6. Butterworth R.F. Portal-systemic encephalopathy: a disorder of neuron-astrocytic metabolic trafficking. Dev. Neurosci. 15:1993;313-319.
7. Cornell-Bell A.H., Finkbeiner S.M., Cooper M.S., Smith S.J. Glutamate induces calcium waves in cultured astrocytes: long-range glial signaling. Science. 247:1990;470-473.
8. Choi D.W. Glutamate neurotoxicity and diseases of the nervous system. Neuron. 1:1988;623-634.
9. D.W. Choi, D.M. Hartley, Calcium and glutamate-induced cortical neuronal death, In: S.G. Waxman (Ed.), Molecular and Cellular Approaches to the Treatment of Neurological Disease, Raven Press, New York, 1993, pp. 23-34.
10. Ferrant M., Cull-Candy S.G. Excitatory amino acid receptor-channels in Purkinje cells in thin cerebellar slices. Proc. R. Soc. Lond. (Biol). 244:1991;179-184.
11. Funovics J.M., Cummings M.G., Shuman L., James J.H., Fisher J.E. An improved non-suture method for porto-caval anastomosis in the rat. Surgery. 77:1975;661-664.
12. Garthwaite G., Williams G.D., Garthwaite J. Glutamate toxicity: an experimental and theoretical analysis. Eur. J. Neurosci. 4:1992;353-360.
13. Garthwaite J., Beaumont P.S. Excitatory amino acid receptors in the parallel fibre pathway in rat cerebellar slices. Neurosci. Lett. 107:1989;151-156.
14. Garthwaite J., Brodbelt A.R. Glutamate as the principal mossy fibre transmitter in rat cerebellum: pharmacological evidence. Eur. J. Neurosci. 2:1989;177-180.
15. Garyfallou V.T., Kohama S.G., Urbanski H.F. Distribution of NMDA and AMPA receptors in the cerebellar cortex of rhesus macaques. Brain Res. 716:1996;22-28.
16. Gasic G.P., Hollmann M. Molecular neurobiology of glutamate receptors. Annu. Rev. Physiol. 54:1992;507-536.
17. 2+ influx into astrocytes. Proc. Natl. Acad. Sci. USA. 87:1990;3454-3458.
18. Grandes P., Ortega F., Streit P. Glutamate-immunoreactive climbing fibres in the cerebellar cortex of the rat. Histochemistry. 101:1994;427-437.
19. Hamberger A., Nystrom B. Extra- and intracellular amino acids in the hippocampus during development of hepatic encephalopathy. Neurochem. Res. 9:1984;1181-1192.
20. Hampson D.R., Huang X.P., Oberdorfer M.D., Goh J.W., Auyeung A., Wenthold R.J. Localization of AMPA receptors in the hippocampus and cerebellum of the rat using an anti-receptor monoclonal antibody. Neuroscience. 50:1992;11-22.
21. Hansson E., Rönnbäck L. Astrocytes in glutamate neurotransmission. FASEB J. 9:1995;343-350.
22. 2+ permeability of KA-AMPA-gated glutamate receptor channels depends on subunit composition. Science. 252:1991;851-853.
23. Horowitz M.E., Schafer D.F., Molnar P., Jones E.A., Blasberg R.G., Patlak C.S., Waggoner J. Increased blood-brain transfer in a rabbit model of acute liver failure. Gastroenterology. 84:1983;1003-1011.
24. Hösli E., Hösli L. Receptors for neurotransmitters on astrocytes in the mammalian central nervous system. Prog. Neurobiol. 40:1990;477-506.
25. Jensen A.M., Chiu S.Y. Fluorescence measurements of changes in intracellular calcium induced by excitatory amino acids in cultured cortical astrocytes. J. Neurosci. 10:1990;1165-1175.
26. Keinänen K., Wisden W., Sommer B., Werner P., Herb A., Verdoorn T.A., Sakmann B., Seeburg P.H. A family of AMPA-selective glutamate receptors. Science. 249:1990;556-560.
27. Laursen H., Diemer N.H. Morphometry of astrocyte and oligodendrocyte ultrastructure after portacaval anastomosis in the rat. Acta Neuropathol. 51:1980;65-70.
28. Le Jeune H., Cécyre D., Rowe W., Meaney M.J., Quirion R. Ionotropic glutamate receptor subtypes in the aged memory-impaired and unimpaired long evans rat. Neuroscience. 74:1996;349-363.
29. Leranth C., Szeidemann Z., Hsu M., Buzsák G. AMPA receptors in the rat and primate hippocampus: a possible absence of GluR2/3 subunits in most interneurones. Neuroscience. 70:1996;631-652.
30. Livingstone A.S., Potvin M., Goresky C.A., Finlayson M.H., Hinchey E.J. Changes in the blood-brain barrier in hepatic coma after hepatectomy in the rat. Gastroenterology. 73:1977;697-704.
31. Lynd-Balta E., Pilcher W.H., Joseph S.A. Distribution of AMPA receptor subunits in the hippocampal formation of temporal lobe epilepsy patients. Neuroscience. 72:1996;15-29.
32. 3H]glutamate uptake in a rat model of chronic hepatic encephalopathy. Neurochem. Int. 28:1996;89-93.
33. Martin L.J., Blackstone C.D., Leveym A.I., Huganir R.L., Price D.L. AMPA glutamate receptor subunits are differentially distributed in rat brain. Neuroscience. 53:1993;327-358.
34. Matute C., Gutierrez-Igarza C., Miledi R. Glutamate receptors in astrocytic end-feet. NeuroReport. 5:1994;1205-1208.
35. Meeldrum B., Garthwaite J. Excitatory amino acid neurotoxicity and neurodegenerative disease. Trends Pharmacol. Sci. 11:1990;379-387.
36. Monaghan D.T., Bridges R.J., Cotman C.W. The excitatory amino acid receptors: their classes, pharmacology, and distintc properties in the function of the central nervous system. Annu. Rev. Pharmacol. Toxicol. 29:1989;365-402.
37. Murphy S., Pearse B. Functional receptors for neurotransmitters on astroglial cells. Neuroscience. 22:1987;381-394.
38. Nagelhus E.A., Lehmann A., Ottersen O.P. Neuronal and glial handling of glutamate and glutamine during hypoosmotic stress: a biochemical and quantitative immunocytochemical analysis using the rat cerebellum as a model. Neuroscience. 72:1996;743-755.
39. Nakanishi S. Molecular diversity of glutamate receptors and implications for brain function. Science. 258:1992;597-603.
40. Norenberg M.D. The role of astrocytes in hepatic encephalopathy. Neurochem. Pathol. 6:1987;13-33.
41. J.W. Olney (1978) Neurotoxicity of excitatory amino acids, In: E.G. McGeer, J.W. Olney, P.L. McGeer (Eds.), Kainic Acid as a Tool in Neurobiology, Raven Press, New York, pp. 37-70.
42. Ottersen O.P. Neurotransmitters in the cerebellum. Rev. Neurol. (Paris). 149:1983;627-636.
43. Petralia R.S., Wenthold R.J. Light and electron immunocytochemical localization of AMPA-selective glutamate receptors in the rat brain. J. Comp. Neurol. 318:1992;329-354.
44. Pilbeam M., Anderson R.McD., Bhathal P.S. The brain in experimental portal systemic encephalopathy. I. Morphological changes in three animal models. J. Pathol. 140:1983;331-345.
45. 2+]. Glia. 13:1995;101-112.
46. Rao V.L.R., Murthy Ch.R.K. Hyparammonaemic alterations in the uptake and release of glutamate and aspartate by rat cerebellar preparations. Neurosci. Lett. 130:1991;49-52.
47. Rogers S.W., Hughes T.E., Hollmann M., Gasic G.P., Deneris E.S., Heinemann S. The characterization and localization of the glutamate receptor subunit GluR1 in the rat brain. J. Neurosci. 11:1991;2713-2724.
48. Rosenberg P.A. Accumulation of extracellular glutamate and neuronal death in astrocyte-poor cortical cultures exposed to glutamine. Glia. 4:1991;91-100.
49. Rothman S.M., Olney J.W. Glutamate and the pathophysiology of hypoxic-ischemic brain damage. Ann. Neurol. 19:1986;105-111.
50. Ryo Y., Miyawaki A., Furuichi T., Mikoshiba K. Expression of the metabotropic glutamate receptor mGluR1α and the ionotropic glutamate receptor GluR1 in the brain during the postnatal development of normal mouse and in the cerebellum from mutant mice. J. Neurosci. Res. 36:1993;19-32.
51. Sandberg M., Butcher S.P., Hagberg H. Extracellular overflow of neuroactive amino acids during severe insulin-induced hypoglycemia: in vivo dialysis of the rat hippocampus. J. Neurochem. 47:1986;178-184.
52. Sandoval M.E., Cotman C.W. Evaluation of glutamate as a neurotransmitter of cerebellar parallel fibers. Neuroscience. 3:1978;199-206.
53. Schmidt W., Wolf G., Grüngreiff K., Meier M., Reum T. Hepatic encephalopathy influences high-affinity uptake of transmitter glutamate and aspartate into hippocampal formation. Metab. Brain Dis. 5:1990;19-31.
54. Sher P.K., Hu S. Increased glutamate uptake and glutamine synthetase activity in neuronal cell cultures surviving chronic hypoxia. Glia. 3:1990;350-357.
55. Somogyi P., Halasy K., Somogyi J., Storm-Mathisen J., Ottersen O.P. Quantification of immunogold labelling reveals enrichment of glutamate in mossy and parallel fibre terminals in cat cerebellum. Neuroscience. 19:1986;1045-1050.
56. Stollberg J., Berg D.K. Neuronal acetylcholine receptors: fate of surface and internal pools in cell culture. J. Neurosci. 7:1987;1809-1815.
57. Suárez I., Bodega G., Arilla E., Rubio M., Villalba R.M., Fernández B. Different response of astrocytes and Bergmann glial cells to portacaval shunt. An immunohistochemical study in the rat cerebellum. Glia. 6:1992;172-179.
58. Suárez I., Bodega G., Arilla E., Fernández B. Region-selective glutamine synthetase expression in the rat central nervous system following portocaval anastomosis. Neuropathol. Appl. Neurobiol. 23:1997;254-261.
59. Takahashi H., Koehler R.C., Brusilow S.W., Traystman R.J. Inhibition of brain glutamine accumulation prevents cerebral edema in hyperammonemic rats. Am. J. Physiol. 261:1991;H825-H829.
60. Takayama C., Nakagawa S., Watanabe M., Mishina M., Inoue Y. Light- and electron-microscopic localization of the glutamate receptor channel δ2 subunit in the mouse Purkinje cell. Neurosci. Lett. 188:1995;89-92.
61. Tang C.M., Orkand R.K. Glutamate depolarization of glial cells in Necturus optic nerve. Neurosci. Lett. 63:1986;300-304.
62. G.L. Westbrook, Glutamate receptors and excitotoxicity, in: S.G. Waxman (Ed.), Molecular and Cellular Approaches to the Treatment of Neurological Disease, Raven Press, New York, 1993, pp. 35-50.