Spermine inhibits [3H]glycine binding at the NMDA receptors from plexiform layers of chick retina

Neurochemical Research

Volumn 23, Issue 11, 1998, Pages 1363-1369

  Calderón, Froylan ^a   López Colomé, Ana María ^a,b,c  

^a INSTITUTO DE FISIOLOGÍA CELULAR   (Mexico)

^b UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^c NONE   (Mexico)

Author keywords

Chick retina; Glycine; NMDA receptors; Spermine

Indexed keywords

GLYCINE; SPERMINE; TRITIUM; DIAGNOSTIC AGENT; N METHYL DEXTRO ASPARTIC ACID RECEPTOR;

ANIMAL TISSUE; ARTICLE; CHICKEN; NEUROMODULATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; RECEPTOR BINDING; RECEPTOR OCCUPANCY; RETINA; ANIMAL; DOSE RESPONSE; DRUG EFFECT; METABOLISM; SYNAPTOSOME; ULTRASTRUCTURE;

ANIMALS; CHICKENS; DOSE-RESPONSE RELATIONSHIP, DRUG; GLYCINE; RECEPTORS, N-METHYL-D-ASPARTATE; RETINA; SPERMINE; SYNAPTOSOMES; TRITIUM;

EID: 0031593807     PISSN: 03643190     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1020794421783     Document Type: Article

References (39)

1. Rock, D. M., and MacDonald, R. L. 1995. Polyamine regulation of N-methyl-D-aspartate receptor channels. Ann. Rev. Pharmacol. Toxicol. 35:463-482.
2. Seiler, N. 1981. Polyamines metabolism and function in brain. Neurochem. Int. 3:95-110.
3. Benveniste, M., and Mayer, M. L. 1993. Multiple effects of spermine on N-methyl-D-aspartic acid receptor responses of rat cultured hippocampal neurones. J. Physiol. 464:131-163.
4. 3H]MK-801 binding to the N-methyl-D-aspartate receptor-ion channel complex by L-glutamate, glycine, and polyamines. J. Neurochem. 51:830-836.
5. Williams, K., Zappia, A. M., Pritchett, D. B., Shen, Y. M., and Molinoff, P. B. 1994. Sensitivity of the N-methyl-D-aspartate receptor to polyamines is controlled by NR2 subunits. Mol. Pharmacol. 45:803-809.
6. Ransom, R. W., and Deschenes, N. L. 1990. Polyamines regulate glycine interaction with the N-methyl-D-aspartate receptor. Synapse 5:294-298.
7. Sacaan, A. I., and Johnson, K. M. 1989. Spermine enhances binding to the glycine site associated with the N-methyl-D-aspartate receptor complex. Mol. Pharmacol. 36:836-839.
8. Rock, D. M., and MacDonald, R. L. 1992. The polyamine spermine has multiple actions on N-methyl-D-aspartate receptor single channel currents in cultured cortical neurons. Mol. Pharmacol. 41: 83-88.
9. Rock, D. M., and MacDonald, R. L. 1992. Spermine and related polyamines produce a voltage-dependent reduction of N-methyl-D-aspartate receptor single-channel conductance. Mol. Pharmacol. 42:157-164.
10. Hollmann, M., and Heinemann, S. 1994. Cloned glutamate receptors. Ann. Rev. Neurosci. 17:31-108.
11. Monyer, H., Sprengel, R., Schoepfer, R., Herb, A., Higuchi, M., Lomeli, H., Burnashev, N., Sakmann, B., and Seeburg, P. H. 1992. Heteromeric NMDA receptors: molecular and functional distinction of subtypes. Science 256:1217-1221.
12. Kutsuwada, T., Kashiwabuchi, N., Mori, H., Sakimura, K., Kushiya E., Araki, K., Meguro, H., Masaki, H., Kumanishi, T., Arakawa, M., and Mishina, M. 1992. Molecular diversity of NMDA receptor channel. Nature 358:36-41.
13. Meguro, H., Mori, H., Araki, K., Kushiya, E., Kutsuwada, T., Yamazaki, M., Kumanishi, T., Arakawa, M., Sakimura, K., and Mishina, M. 1992. Functional characterization of a heteromeric NMDA receptor channel expressed from cloned cDNAs. Nature 357:70-74.
14. Ishii, T., Moriyoshi, K., Sugihara, H., Sakurada, K., Kadotani, H., Yokoi, M., Akasawa, C., Shigemoto, R., Mizuno, N., Masu, M., and Nakanishi, S. 1993. Molecular characterization of the family of the N-methyl-D-aspartate receptor subunits. J. Biol. Chem. 268: 2836-2843.
15. Nakanishi, S. 1992. Molecular diversity of glutamate receptors and implications for brain function. Science 258:597-603.
16. López-Colomé, A. M. 1986. Amino acids as excitatory transmitters in the retina. Pages 143-157, in P. J. Roberts, J. Storm-Mathisen and H. F. Bradford (eds.), Excitatory amino acids, Macmillan Press, London.
17. Brandstätter, J. H., Hartveit, E., Sassoè-Pognetto, M., and Wässle, H. 1994. Expression of NMDA and high-affinity kainate receptor subunit mRNAs in the adult rat retina. Eur. J. Neurosci. 6:1100-1112.
18. Koulen, P., Sassoe-Pognetto, M., Grunert, U., and Wässle, H. 1996. Selective clustering of GABA(A) and glycine receptors in the mammalian retina. J. Neurosci. 6:2127-2140.
19. Lombardi, G., Moroni, F., and Moroni, F. 1994. Glutamate receptor antagonists protect against ischemia-induced retinal damage. Eur. J. Pharmacol. 271:489-495.
20. Chen, J., Graham, S., Moroni, F., and Simon, R. 1993. A dose-response study of a glycine receptor antagonist in focal ischemia. J. Pharmacol. Exp. Ther. 267, 937.
21. Pellegrini-Giampietro, D., Cozzi, A., and Moroni, F. 1993. 7-Cl-Thiokynurenic acid: a glycine antagonist and free radical scavenger that reduced CA1 ischemic damage in vivo. Soc. Neurosci. Abstr. 19:1645.
22. López-Colomé, A. M., and Somohano, F. 1992. N-methyl-D-aspartate receptors in the retina: 3-[(±)-2-carboxypiperazin-4-yl]-propyl-1-phosphonic acid (CPP) binding studies. Neuropharmacology 6:577-584.
23. Boje, K. M., Skolnick, P., Raber, J., Fletcher, R. T., and Chader, G. 1992. Strychnine-insensitive glycine receptors in embryonic chick retina: characteristics and modulation of NMDA neurotoxicity. Neurochem. Int. 4:473-486.
24. López-Colomé, A. M., Salceda, R., and Pasantes-Morales, H. 1978. Potassium-stimulated release of GABA, glycine and taurine from the chick retina. Neurochem. Res. 3:431-441.
25. Lowry, O. H., Rosebrough, W. H., Farr, A. L., and Randall, R. S. 1951. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193:265-275.
26. López-Colomé, A. M., Calderón, F., and Rodriguez, A. 1995. Modulatory effects of polyamines on strychnine-insensitive glycine receptors in chick retina. Soc. Neurosci. Abstr. Vol. 21, p. 145.20.
27. Weiland, G. A., and Molinoff, P. B. 1981. Quantitative analysis of drug-receptor interactions. I. Determination of kinetic and equilibrium properties. Life Sci. 29:313-330.
28. Williams, K., Romano, C., Dichter, M. A., and Molinoff, P. B. 1991. Modulation of the NMDA receptor by polyamines. Life Sci. 48:469-498.
29. Ballas, S. K., Mohandas, N., Marton, L. J., and Shohet, S. B. 1983. Stabilization of erythrocyte membranes by polyamines. Proc. Natl. Acad. Sci. USA. 80:1942-1946.
30. 3H]spermidine in synaptic membranes of rat brain. Brain Res. 563:17-27.
31. Kashiwagi, K., Fukuchi, J., Chao, J., Igarashi, K., and Williams, K. 1996. An aspartate residue in the extracellular loop of the N-methyl-D-aspartate receptor controls sensitivity to spermine and protons. Mol. Pharmacol. 49:1131-1141.
32. Gallagher, M. J., Huang, H., Pritchett, D. B., and Lynch, D. R. 1996. Interactions between ifenprodil and the NR2B subunit of the N-methyl-D-aspartate receptor. J. Biol. Chem. 271:9603-9611.
33. Rao, T. S., Cler, J. A, Mick, S. J., Iyengar, S., and Wood, P. L. 1991. Polyamines modulate events mediated by the N-methyl-D-aspartate (NMDA) receptor complex through an ifenprodil-insensitive pathway: in vivo measurements of cyclic GMP in the cerebellum. Neuropharmacology 30:567-573.
34. 3H]MK801 binding to rat brain N-methyl-D-aspartate receptors. J. Neurochem. 56:1731-1740.
35. Williams, K. 1995. Pharmacological properties of recombinant N-methyl-D-aspartate (NMDA) receptors containing the ε4 (NR2D) subunit. Neurosci. Lett. 184:181-184.
36. Wafford, K. A., Bain, C. J., Bourdelles, B. L., Whiting, P. J., and Kemp, J. A. 1993. Preferential co-assembly of recombinant NMDA receptors composed of three different subunits. Neuroreport. 4:1347-1349.
37. Luo, J., Wang, Y., Yasuda, R. P., Dunah, A. W., and Wolfe, B. B. 1997. The majority of N-methyl-D-aspartate receptor complexes in rat cerebral cortex contain at least three different subunits (NR1/NR2A/NR2B). Mol. Pharmacol. 51:79-86.
38. Guylaine, M. D., Bennett, M. V. L., and Zukin, S. 1993. Splice variants of the N-methyl-D-aspartate receptor NR1 identify domains involved in regulation by polyamines and protein kinase C. Proc. Natl. Acad. Sci. USA. 90:6731-6735.
39. Traynelis, S. F., Hartley, M., and Heinemann, S. F. 1995. Control of proton sensitivity of the NMDA receptor by RNA splicing and polyamines. Science 268:873-876.