GluR2/3, NMDAE1 and GABAA receptors in Creutzfeldt-Jakob disease

Acta Neuropathologica

Volumn 106, Issue 4, 2003, Pages 311-318

  Ferrer, I ^a,b   Puig, B ^a,b  

^a HOSPITAL UNIVERSITARI DE BELLVITGE   (Spain)

^b UNIVERSITY OF BARCELONA   (Spain)

Author keywords

amino 3 hydro 5methyl 4 isoxazole propionic acid; aminobutyric acid receptors; Creutzfeldt Jakob disease; Glutamate receptors; N methyl D aspartate

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR; 4 AMINOBUTYRIC ACID A RECEPTOR ALPHA 1; AMPA RECEPTOR; GLUTAMATE RECEPTOR; IONOTROPIC RECEPTOR; METHIONINE; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR 2A; NEUROTRANSMITTER RECEPTOR; PRION PROTEIN; UNCLASSIFIED DRUG; GLUTAMATE RECEPTOR IONOTROPIC, AMPA 2; GLUTAMATE RECEPTOR IONOTROPIC, AMPA 3;

ADULT; AGED; ARTICLE; BRAIN CORTEX; BRAIN DEGENERATION; CELL LOSS; CENTRAL NERVOUS SYSTEM; CEREBELLUM CORTEX; CLINICAL ARTICLE; CODON; CONTROLLED STUDY; CORRELATION ANALYSIS; CREUTZFELDT JAKOB DISEASE; DENTATE GYRUS; ENTORHINAL CORTEX; FEMALE; FRONTAL LOBE; GRANULAR CELL; HIPPOCAMPUS; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; IMMUNOREACTIVITY; MALE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PURKINJE CELL; SYNAPTIC TRANSMISSION; BRAIN; CASE CONTROL STUDY; COMPARATIVE STUDY; METABOLISM; METHODOLOGY; MIDDLE AGED; PATHOLOGY; PRION;

AGED; BRAIN; CASE-CONTROL STUDIES; CREUTZFELDT-JAKOB SYNDROME; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MIDDLE AGED; PRIONS; RECEPTORS, AMPA; RECEPTORS, GABA-A; RECEPTORS, N-METHYL-D-ASPARTATE;

EID: 0142125765     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00401-003-0732-z     Document Type: Article

References (36)

1. Aguglia U, Oliveri RL, Gambardella A, Talerico G, Zappia M, De Sarro GB, Quattrone A (1996) Functional preservation of nezodiazepine receptors of the primary somatosensory cortex in Creutzfeldt-Jakob disease: a pharmacologic-evoked potential study. Clin Neuropharmacol 19:87-91
2. A receptors: classification on the basis of subunit structure and receptor function. Pharmacol Rev 50:291-313
3. Belichenko PV, Brown D, Jeffrey M, Fraser JR (2000) Dendritic and synaptic alterations of hippocampal pyramidal neurones in scrapie-infected mice. Neuropathol Appl Neurobiol 26:143-149
4. Bignami A, Parry HB (1972) Electron microscopic studies on the brain of sheep with natural scrapie. II. The small nerve processes in neuronal degeneration. Brain 95:487-494
5. Borges K, Digledine R (1998) AMPA receptors: molecular and functional diversity. Prog Brain Res 116:153-170
6. Brown D, Halliday W, Jeffrey M, Fraser J (1997) Visualising scrapie infected and normal neurons in the murine hippocampus using Golgi impregnation and confocal imaging of intracellular dye. J Cell Pathol 2:131-136
7. Brown DR, Herms JW, Schmidt B, Kretzschmar HA (1997) PrP and β amyloid fragments activate different neurotoxic mechanisms in cultured mouse cells. Eur J Neurosci 9:1162-1169
8. Catalá I, Ferrer I, Galofré E, Fábregues I (1988) Decreased numbers of dendritic spines on cortical pyramidal neurons in dementia. A quantitative Golgi study in biopsy samples. Hum Neurobiol 6:255-259
9. Chou SM, Payne WN, Gibbs CJ, Gajdusek DC (1980) Transmission and scanning electron microscopy of spongiform change in Creutzfeldt-Jakob disease. Brain 103:885-904
10. Collinge J, Whittington MA, Sidle KCL, Smith J, Palmer MS, Clarke AR, Jeffreys JGR (1994) Prion protein is necessary for normal synaptic function. Nature 370:295-297
11. Dingledine R, Borges K, Bowie D, Traynelis SF (1999) The glutamate receptor ion channels. Pharmacol Rev 51:7-61
12. Ferrer I, Costa F, Grau Veciana JM (1981) Creutzfeldt-Jakob disease: a Golgi study. Neuropathol Appl Neurobiol 7:237-242
13. Ferrer I, Casas R, Rivera R (1993) Parvalbumin-immunoreactive cortical neurons in Creutzfeldt-Jakob disease. Ann Neurol 34:864-866
14. Gonatas NK, Terry RD, Weiss M (1965) Electron microscopic study in two cases of Jakob-Creutzfeldt disease. J Neuropathol Exp Neurol 24:575-598
15. Güentchev M, Hainfellner JA, Trabattoni GR, Budka H (1997) Distribution of parvalbumin-immunoreactive neurons in brain correlates with hippocampal and temporal cortical pathology in Creutzfeldt-Jakob disease. J Neuropathol Exp Neurol 56:1119-1124
16. Güentchev M, Groschup MH, Kodek R, Liberski PP, Budka H (1998) Severe, early and selective loss of a subpopulation of GABAergic inhibitory neurons in experimental transmissible spongiform encephalopathies. Brain Pathol 8:615-623
17. Hogan RN, Baringer JR, Prusiner SB (1987) Scrapie infection diminishes spines and increases varicosities of dendrites in hamsters: a quantitative Golgi study. J Neuropathol Exp Neurol 46:461-473
18. Hollmann M, Heinemann S (1994) Cloned glutamate receptors. Annu Rev Neurosci 17:31-108
19. Ito Y, Amano T, Shimizu T, Hashimoto J, Kubo A, Fukuuchi Y (1998) Single-photon emission computed tomography image of benzodiazepine receptors in a patient with Creutzfeldt-Jakob disease. Intern Med 37:896-900
20. A receptors: no physical association? NeuroReport 7:77-80
21. A-receptor subtypes: clinical efficiency and selectivity of benzodiazepine site ligands. Ann Med 29:275-282
22. Lampert PW, Gajdusek DC, Gibbs CJ Jr (1971) Experimental spongiform encephalopathy (Creutzfeldt-Jakob disease) in chimpanzees. Electron microscopical studies. J Neuropathol Exp Neurol 30:20-32
23. Landis DNMD, Williams RS, Masters CL (1981) Golgi and electron microscopic studies of spongiform encephalopathies. Neurology 31:538-549
24. Liberski P, Yanigahira R, Asher DM, Gibbs CJ, Gajdusek DC (1990) Reevaluation of the ultrastructural pathology of experimental Creutzfeldt-Jakob disease. Brain 113:121-137
25. A receptor channels. Annu Rev Neurosci 17:569-602
26. Machado-Salas JP (1986) Dendritic and axonal spherules in the neocortex of a patient with Creutzfeldt-Jakob disease (CJD): Golgi and electron-microscopical investigation-neurobiological significance. Clin Neuropathol 5:176-184
27. Marin O, Vial JD (1964) Neuropathological and ultrastructural findings in two cases of subacute spongiform encephalopathy. Acta Neuropathol 4:218-229
28. Sc)-induced toxicity in rat cortical cell cultures. Eur J Pharmacol 246:261-267
29. Nakanishi S, Nakajima Y, Masu M, Ueda Y, Ankara K, Watanaabe D, Yamaguchi S, Kawabata S, Okada M (1998) Glutamate receptors: brain function and signal transduction. Brain Res Rev 26:230-235
30. Olney JW, Ishimaru MJ (1999) Excitotoxic cell death. In: Koliatsos VE, Ratan RR (eds) Cell death and diseases of the nervous system. Humana Press, Totowa, pp 197-218
31. Ozawa S, Kamiya H, Tsuzuki K (1998) Glutamate receptors in the mammalian central nervous system. Prog Neurobiol 54: 581-618
32. Scallet AC, Ye X (1997) Excitotoxic mechanisms of neurodegeneration in transmissible spongiform encephalopathies. Ann NY Acad Sci 15:194-205
33. Schoepfer R, Monyer H, Sommer B, Wisden W, Sprengel R, Kuner T, Lomeli H, Herb A, Kohler M, Burnashev N, Gunther W, Ruppersberg P, Seeburg P (1994) Molecular biology of glutamate receptors. Prog Neurobiol 42:353-357
34. Tateishi J, Sato Y, Ohta M (1983) Creutzfeldt-Jakob disease in humans and laboratory animals. Prog Neuropathol 5:195-221
35. Wang Y, TesFaye E, Yasuda RP, Mash DC, Armstrong DM, Wolfe BB (2000) Effects of post-mortem delay on subunits of ionotropic glutamate receptors in human brain. Mol Brain Res 80:123-131
36. Yoneda Y, Kuramoto N, Kitayama T, Hinoi E (2001) Consolidation of transient ionotropic glutamate signals through nuclear transcription factors in the brain. Prog Neurobiol 63:697-719