Kainate-triggered currents in Xenopus oocytes injected with chick retinal membrane fragments: Effect of guanine nucleotides

Investigative Ophthalmology and Visual Science

Volumn 44, Issue 7, 2003, Pages 3124-3129

  Burgos, Javier S ^a   Aleu, Jordi ^b   Barat, Ana ^a   Solsona, Carles ^b   Marsal, Jordi ^b   Ramírez, Galo ^a  

^a UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

^b UNIVERSITY OF BARCELONA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

1 (4 AMINOPHENYL) 4 METHYL 7,8 METHYLENEDIOXY 5H 2,3 BENZODIAZEPINE; 2 AMINO 7 PHOSPHONOHEPTANOIC ACID; 6,7 DINITRO 2,3 QUINOXALINEDIONE; AMPA RECEPTOR; GAMMA DEXTRO GLUTAMYLAMINOMETHYLSULFONIC ACID; GUANINE NUCLEOTIDE; GUANOSINE 5' O (2 THIODIPHOSPHATE); GUANOSINE 5' O (3 THIOTRIPHOSPHATE); GUANOSINE PHOSPHATE; GUANYLYLIMIDODIPHOSPHATE; KAINIC ACID; KAINIC ACID RECEPTOR;

ANIMAL CELL; ARTICLE; CHICKEN; CONCENTRATION RESPONSE; CONTROLLED STUDY; ELECTROPHYSIOLOGY; IMMUNOFLUORESCENCE; MICROINJECTION; NONHUMAN; OOCYTE; PRIORITY JOURNAL; RETINA; RETINA MEMBRANE FRAGMENT; VOLTAGE CLAMP; XENOPUS;

ANIMALS; CELL MEMBRANE; CHICKENS; DOSE-RESPONSE RELATIONSHIP, DRUG; ELECTRIC CONDUCTIVITY; ELECTROPHYSIOLOGY; EXCITATORY AMINO ACID ANTAGONISTS; FEMALE; GLUTAMINE; GUANINE NUCLEOTIDES; KAINIC ACID; MEMBRANE POTENTIALS; MICROINJECTIONS; OOCYTES; PATCH-CLAMP TECHNIQUES; RABBITS; RECEPTORS, AMPA; RETINA; XENOPUS LAEVIS;

EID: 0037562530     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: 10.1167/iovs.02-0669     Document Type: Article

References (42)

1. Gibson BL, Reif-Lehrer L. In vitro effects of kainate on embryonic and post-hatching chick retina. Dev Brain Res. 1984;15:97-103.
2. Olney JW, Price MT, Samson L, Labruyere J. The role of specific ions in glutamate neurotoxicity. Neurosci Lett. 1986;65:65-71.
3. Zeevalk GD, Hyndman AG, Nicklas WJ. Excitatory amino acid-induced toxicity in chick retina: amino acid release, histology and effects of chloride channel blockers. J Neurochem. 1989;53:1610-1619.
4. 2+ entry via AMPA/KA receptors in the embryonic chick retina. Eur J Neurosci. 1996;8:2499-2510.
5. - and inhibitory transmitters. Mol Pharmacol. 1998;53:654-572.
6. Romano C, Chen Q, Olney JW. The intact isolated (ex-vivo) retina as a model system for the study of excitotoxicity. Prog Retinal Eye Res. 1998;17:465-483.
7. Burgos JS, Barat A, Souza DO, Ramírez G. Guanine nucleotides protect against kainate toxicity in an ex vivo chick retinal preparation. FEBS Lett. 1998;430:176-180.
8. 2+ influx in chick embryo retinal explants. Neuroreport. 2000;11:2303-2305.
9. 2O influx in chick embryonic retina. Neuroreport. 2000;11:3779-3782.
10. 2+-dependent kainate excitotoxicity in the chick embryonic neural retina ex vivo. Neuroreport. 2000;11:3855-3858.
11. Monahan JB, Hood WF, Michel J, Compton, RP. Effects of guanine nucleotides on N-methyl-D-aspartate receptor-ligand interactions. Mol Pharmacol. 1988;34:111-116.
12. Baron BN, Dudley MW, McCarty DR, Miller FP, Reynolds IJ, Schmidt CJ. Guanine nucleotides are competitive inhibitors of N-methyl-D-aspartate at its receptor site both in vitro and in vivo. J Pharmacol Exp Ther. 1989;250:162-169.
13. Budson AE, Jackson PS, Lipton SA. GDPβS antagonizes whole-cell responses to excitatory amino acids. Brain Res. 1991;548:346-348.
14. Souza DO, Ramírez G. Effect of guanine nucleotides on kainic acid binding and on adenylate cyclase in chick optic tectum and cerebellum. J Mol Neurosci. 1991;3:39-45.
15. Gorodinsky A, Paas Y, Teichberg VI. A ligand binding study of the interactions of guanine nucleotides with non-NMDA receptors. Neurochem Int. 1993;23:285-291.
16. Paas Y, Devillers-Thiéry A, Changeux J-P, Medevielle F, Teichberg VI. Identification of an extracellular motif involved in the binding of guanine nucleotides by a glutamate receptor. EMBO J. 1996;15:1548-1556.
17. Dev KK, Roberts P, Henley JM. Characterisation of the interaction between guanyl nucleotides and AMPA receptors in rat brain. Neuropharmacology. 1996;35:1583-1593.
18. Malcon C, Achaval M, Komlos F, et al. GMP protects against quinolinic acid-induced loss of NADPH-diaphorase-positive cells in the rat striatum. Neurosci Lett. 1997;225:145-148.
19. 3H]GppNHp to extracellular membrane receptors in chick cerebellum: possible involvement of kainic acid receptors. FEBS Lett. 1997;406:114-118.
20. Regner A, Ramírez G, Belló-Klein A, Souza D. Effects of guanine nucleotides on glutamate-induced chemiluminescence in rat hippocampal slices submitted to hypoxia. Neurochem Res. 1998;23:523-528.
21. - channels in Xenopus oocytes injected with Torpedo electroplaque membranes. Proc Natl Acad Sci USA. 1995;92:5224-5228.
22. Aleu J, Barat A, Burgos JS, Solsona C, Marsal J, Ramírez G. Guanine nucleotides, including GMP, antagonize kainate responses in Xenopus oocytes injected with chick cerebellar membranes. J Neurochem. 1999;72:2170-2176.
23. 2+-dependent acetylcholine release system in Xenopus oocytes microinjected with synaptic plasma membranes and synaptic vesicles. J Neurosci Res. 1996;44:106-114.
24. Dumont JN. Oogenesis in Xenopus laevis (Daudin). J Morphol 1972;136:153-180.
25. Sumikawa K, Parker I, Miledi R. Expression of neurotransmitter receptors and voltage-activated channels from brain mRNA in Xenopus oocytes. Methods Neurosci. 1989;1:30-63.
26. Harlow E, Lane D. Antibodies. A Laboratory Manual. New York: Cold Spring Harbor Laboratory; 1988.
27. Zhou N, Hammerland LG, Parks TN. γ-D-glutamylaminomethyl sulfonic acid (GAMS) distinguishes kainic acid- from AMPA-induced responses in Xenopus oocytes expressing chick brain glutamate receptors. Neuropharmacology. 1993;8:767-775.
28. Kiskin NI, Krishtal OA, Tsyndrenko AY. Excitatory amino acid receptors in hippocampal neurons: kainate fails to desensitize them. Neurosci Lett. 1986;63:225-230.
29. Barnard EA, Henley JM. The non-NMDA receptors: types, structure and molecular biology. Trends Pharmacol Sci. 1990;11:500-507.
30. Michaelis EK. Molecular biology of glutamate receptors in the central nervous system and their role in excitotoxicity, oxidative stress and aging. Prog Neurobiol. 1998;54:369-415.
31. Zhou LM, Gu ZQ, Costa AM, et al. (2S, 4R)-4-methylglutamic acid (SYM 2081): a selective, high affinity ligand for kainate receptors. J Pharmacol Exp Ther. 1997;280:422-427.
32. Rothstein JD. Excitotoxicity hypothesis. Neurology. 1996;47(suppl 4):S19-S25.
33. Fischer AJ, Seltner RL, Poon J, Stell WK. Immunocytochemical characterization of quisqualic acid- and N-methyl-D-aspartate-induced excitotoxicity in the retina of chicks. J Comp Neurol. 1998;393:1-15.
34. Ientile R, Macaione V, Teletta M, Pedale S, Torre V, Macaione S. Apoptosis and necrosis occurring in excitotoxic cell death in isolated chick embryo retina. J Neurochem. 79:71-78, 2001.
35. Fischer AJ, Seltner RL, Stell WK. N-methyl-D-aspartate-induced excitotoxicity causes myopia in hatched chicks. Can J Ophthalmol. 1997;32:373-377.
36. Dreyer EB, Zurakowski D, Schumer RA, Podos SM, Lipton SA. Elevated glutamate levels in the vitreous body of humans and monkeys with glaucoma. Arch Ophthalmol. 1996;114:299-305.
37. Massey SC, Redburn DA. Transmitter circuits in the vertebrate retina. Prog Neurobiol. 1987;28:55-96.
38. Huba R, Hofmann H-D. Transmitter-gated currents of GABAergic amacrine-like cells in chick retinal cultures. Vis Neurosci. 1991;6:303-314.
39. Ferreira IL, Duarte CB, Carvalho AP. Kainate-induced retina amacrine-like cell damage is mediated by AMPA receptors. Neuroreport. 1998;9:3471-3475.
40. 2+-permeable AMPA receptors in delayed neurodegeneration. Cold Spring Harbor Symp Quant Biol. 1996;61:373-384.
41. Klethi J, Urban PF, Mandel P. Free nucleotides in retina. FEBS Lett. 1970;8:119-121.
42. Mendieta J, Ramírez G, Gago, F. Molecular dynamics simulations of the conformational changes of the glutamate receptor ligand-binding core in the presence of glutamate and kainate. Proteins. 2001;44:460-469.