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. 1994 Mar 15;475(3):439–453. doi: 10.1113/jphysiol.1994.sp020084

Metabotropic glutamate response in acutely dissociated hippocampal CA1 pyramidal neurones of the rat.

T Shirasaki 1, N Harata 1, N Akaike 1
PMCID: PMC1160396  PMID: 7911830

Abstract

1. The metabotropic glutamate (mGlu) response was investigated in dissociated rat hippocampal CA1 pyramidal neurones using conventional and nystatin-perforated whole-cell modes of the patch recording configuration. 2. In the perforated patch recording configuration, the application of glutamate (Glu), quisqualate (QA), aspartate (Asp) and N-methyl-D-aspartate (NMDA) induced a slow outward current superimposed on a fast ionotropic inward current, whereas alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) and kainate (KA) induced only an ionotropic inward current at a holding potential (VH) of -20 mV. A specific agonist of the mGlu receptor (mGluR), trans-1-aminocyclopentane-1,3-dicarboxylate (tACPD), induced an outward current in approximately 80% of the neurones tested. Asp- and NMDA-induced outward currents were antagonized by D-2-amino-5-phosphonopentanoate (D-AP5) whereas Glu-, QA- and tACPD-induced outward currents were not antagonized by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), 6,7-dinitroquinoxaline-2,3-dione (DNQX) and D-AP5, indicating that the mGlu response is an outward current component. 3. L-2-Amino-3-phosphonopropionate (L-AP3) and DL-2-amino-4-phosphonobutyrate (AP4) did not block the mGlu response. 4. The relative potencies of mGlu agonists were QA > Glu > tACPD. The threshold and EC50 values of metabotropic outward currents were 10-100 times lower than those of the ionotropic inward current (iGlu response). 5. The reversal potential of the mGlu response (EmGlu) was close to EK (K+ equilibrium potential), and it shifted 59.5 mV for a tenfold change in extracellular K+ concentration. 6. In Ca(2+)-free external solution, the mGlu response was elicited by an initial application of Glu, but subsequent applications failed to induce the response. There was also an increase in the intracellular free Ca2+ concentration ([Ca2+]i) during the application of Glu and QA but not of AMPA, indicating Ca2+ release from an intracellular Ca2+ store. 7. During the activation of a Ca(2+)-dependent K+ current (IK(Ca)) by inositol trisphosphate (IP3) in the internal solution, the mGlu response was suppressed. Addition of GDP-beta-S, neomycin or heparin to the internal solution also suppressed the mGlu response, but staurosporine had no effect. The mGlu response was abolished by pretreatment with either caffeine or ryanodine, but treatment with pertussis toxin (IAP) for 6-8 h had no effect. 8. The mGlu response was suppressed by tetraethylammonium, but not by either apamin or iberiotoxin, suggesting that intermediate-conductance Ca(2+)-dependent K+ (KCa+) channels are involved.(ABSTRACT TRUNCATED AT 400 WORDS)

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Selected References

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  1. Abe T., Sugihara H., Nawa H., Shigemoto R., Mizuno N., Nakanishi S. Molecular characterization of a novel metabotropic glutamate receptor mGluR5 coupled to inositol phosphate/Ca2+ signal transduction. J Biol Chem. 1992 Jul 5;267(19):13361–13368. [PubMed] [Google Scholar]
  2. Abraham W. C., Wickens J. R. Heterosynaptic long-term depression is facilitated by blockade of inhibition in area CA1 of the hippocampus. Brain Res. 1991 Apr 19;546(2):336–340. doi: 10.1016/0006-8993(91)91498-p. [DOI] [PubMed] [Google Scholar]
  3. Adamson P., Hajimohammadreza I., Brammer M. J., Campbell I. C., Meldrum B. S. Presynaptic glutamate/quisqualate receptors: effects on synaptosomal free calcium concentrations. J Neurochem. 1990 Dec;55(6):1850–1854. doi: 10.1111/j.1471-4159.1990.tb05767.x. [DOI] [PubMed] [Google Scholar]
  4. Akaike N., Takahashi K. Tetrodotoxin-sensitive calcium-conducting channels in the rat hippocampal CA1 region. J Physiol. 1992 May;450:529–546. doi: 10.1113/jphysiol.1992.sp019141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Baskys A., Malenka R. C. Agonists at metabotropic glutamate receptors presynaptically inhibit EPSCs in neonatal rat hippocampus. J Physiol. 1991 Dec;444:687–701. doi: 10.1113/jphysiol.1991.sp018901. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Borden L. A., Farb D. H. Mechanism of gamma-aminobutyric acid/benzodiazepine receptor turnover in neuronal cells: evidence for nonlysosomal degradation. Mol Pharmacol. 1988 Sep;34(3):354–362. [PubMed] [Google Scholar]
  7. Charpak S., Gähwiler B. H., Do K. Q., Knöpfel T. Potassium conductances in hippocampal neurons blocked by excitatory amino-acid transmitters. Nature. 1990 Oct 25;347(6295):765–767. doi: 10.1038/347765a0. [DOI] [PubMed] [Google Scholar]
  8. Collingridge G. L., Lester R. A. Excitatory amino acid receptors in the vertebrate central nervous system. Pharmacol Rev. 1989 Jun;41(2):143–210. [PubMed] [Google Scholar]
  9. Desai M. A., Conn P. J. Selective activation of phosphoinositide hydrolysis by a rigid analogue of glutamate. Neurosci Lett. 1990 Feb 5;109(1-2):157–162. doi: 10.1016/0304-3940(90)90555-n. [DOI] [PubMed] [Google Scholar]
  10. Dolphin A. C., Scott R. H. Calcium channel currents and their inhibition by (-)-baclofen in rat sensory neurones: modulation by guanine nucleotides. J Physiol. 1987 May;386:1–17. doi: 10.1113/jphysiol.1987.sp016518. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dumuis A., Pin J. P., Oomagari K., Sebben M., Bockaert J. Arachidonic acid released from striatal neurons by joint stimulation of ionotropic and metabotropic quisqualate receptors. Nature. 1990 Sep 13;347(6289):182–184. doi: 10.1038/347182a0. [DOI] [PubMed] [Google Scholar]
  12. Ebihara S., Akaike N. Potassium currents operated by thyrotrophin-releasing hormone in dissociated CA1 pyramidal neurones of rat hippocampus. J Physiol. 1993 Dec;472:689–710. doi: 10.1113/jphysiol.1993.sp019967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Evans R. H., Francis A. A., Jones A. W., Smith D. A., Watkins J. C. The effects of a series of omega-phosphonic alpha-carboxylic amino acids on electrically evoked and excitant amino acid-induced responses in isolated spinal cord preparations. Br J Pharmacol. 1982 Jan;75(1):65–75. doi: 10.1111/j.1476-5381.1982.tb08758.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Fagni L., Bossu J. L., Bockaert J. Activation of a Large-conductance Ca2+-Dependent K+ Channel by Stimulation of Glutamate Phosphoinositide-coupled Receptors in Cultured Cerebellar Granule Cells. Eur J Neurosci. 1991;3(8):778–789. doi: 10.1111/j.1460-9568.1991.tb01674.x. [DOI] [PubMed] [Google Scholar]
  15. Goh J. W., Pennefather P. S. A pertussis toxin-sensitive G protein in hippocampal long-term potentiation. Science. 1989 May 26;244(4907):980–983. doi: 10.1126/science.2543072. [DOI] [PubMed] [Google Scholar]
  16. Grynkiewicz G., Poenie M., Tsien R. Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem. 1985 Mar 25;260(6):3440–3450. [PubMed] [Google Scholar]
  17. Henley J. M., Johnston G. A. Vintage amino acid meeting describes new tools for amino acid research, subtypes of metabotropic receptors. Trends Pharmacol Sci. 1991 Oct;12(10):357–359. doi: 10.1016/0165-6147(91)90600-w. [DOI] [PubMed] [Google Scholar]
  18. Henzi V., MacDermott A. B. Characteristics and function of Ca(2+)- and inositol 1,4,5-trisphosphate-releasable stores of Ca2+ in neurons. Neuroscience. 1992;46(2):251–273. doi: 10.1016/0306-4522(92)90049-8. [DOI] [PubMed] [Google Scholar]
  19. Hoch W., Betz H., Becker C. M. Primary cultures of mouse spinal cord express the neonatal isoform of the inhibitory glycine receptor. Neuron. 1989 Sep;3(3):339–348. doi: 10.1016/0896-6273(89)90258-4. [DOI] [PubMed] [Google Scholar]
  20. Houamed K. M., Kuijper J. L., Gilbert T. L., Haldeman B. A., O'Hara P. J., Mulvihill E. R., Almers W., Hagen F. S. Cloning, expression, and gene structure of a G protein-coupled glutamate receptor from rat brain. Science. 1991 May 31;252(5010):1318–1321. doi: 10.1126/science.1656524. [DOI] [PubMed] [Google Scholar]
  21. Hu G. Y., Hvalby O., Walaas S. I., Albert K. A., Skjeflo P., Andersen P., Greengard P. Protein kinase C injection into hippocampal pyramidal cells elicits features of long term potentiation. 1987 Jul 30-Aug 5Nature. 328(6129):426–429. doi: 10.1038/328426a0. [DOI] [PubMed] [Google Scholar]
  22. Irving A. J., Collingridge G. L., Schofield J. G. Interactions between Ca2+ mobilizing mechanisms in cultured rat cerebellar granule cells. J Physiol. 1992 Oct;456:667–680. doi: 10.1113/jphysiol.1992.sp019360. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Izumi Y., Clifford D. B., Zorumski C. F. 2-Amino-3-phosphonopropionate blocks the induction and maintenance of long-term potentiation in rat hippocampal slices. Neurosci Lett. 1991 Jan 28;122(2):187–190. doi: 10.1016/0304-3940(91)90854-m. [DOI] [PubMed] [Google Scholar]
  24. Kelso S. R., Nelson T. E., Leonard J. P. Protein kinase C-mediated enhancement of NMDA currents by metabotropic glutamate receptors in Xenopus oocytes. J Physiol. 1992 Apr;449:705–718. doi: 10.1113/jphysiol.1992.sp019110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Kessler M., Baudry M., Lynch G. Use of cystine to distinguish glutamate binding from glutamate sequestration. Neurosci Lett. 1987 Oct 16;81(1-2):221–226. doi: 10.1016/0304-3940(87)91002-0. [DOI] [PubMed] [Google Scholar]
  26. Lester R. A., Jahr C. E. Quisqualate receptor-mediated depression of calcium currents in hippocampal neurons. Neuron. 1990 May;4(5):741–749. doi: 10.1016/0896-6273(90)90200-y. [DOI] [PubMed] [Google Scholar]
  27. Masu M., Tanabe Y., Tsuchida K., Shigemoto R., Nakanishi S. Sequence and expression of a metabotropic glutamate receptor. Nature. 1991 Feb 28;349(6312):760–765. doi: 10.1038/349760a0. [DOI] [PubMed] [Google Scholar]
  28. McGuinness N., Anwyl R., Rowan M. The effects of trans-ACPD on long-term potentiation in the rat hippocampal slice. Neuroreport. 1991 Nov;2(11):688–690. doi: 10.1097/00001756-199111000-00014. [DOI] [PubMed] [Google Scholar]
  29. Murphy S. N., Miller R. J. A glutamate receptor regulates Ca2+ mobilization in hippocampal neurons. Proc Natl Acad Sci U S A. 1988 Nov;85(22):8737–8741. doi: 10.1073/pnas.85.22.8737. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Murphy S. N., Miller R. J. Two distinct quisqualate receptors regulate Ca2+ homeostasis in hippocampal neurons in vitro. Mol Pharmacol. 1989 May;35(5):671–680. [PubMed] [Google Scholar]
  31. Nakanishi S. Molecular diversity of glutamate receptors and implications for brain function. Science. 1992 Oct 23;258(5082):597–603. doi: 10.1126/science.1329206. [DOI] [PubMed] [Google Scholar]
  32. Nicoletti F., Wroblewski J. T., Fadda E., Costa E. Pertussis toxin inhibits signal transduction at a specific metabolotropic glutamate receptor in primary cultures of cerebellar granule cells. Neuropharmacology. 1988 Jun;27(6):551–556. doi: 10.1016/0028-3908(88)90174-8. [DOI] [PubMed] [Google Scholar]
  33. Nicoletti F., Wroblewski J. T., Novelli A., Alho H., Guidotti A., Costa E. The activation of inositol phospholipid metabolism as a signal-transducing system for excitatory amino acids in primary cultures of cerebellar granule cells. J Neurosci. 1986 Jul;6(7):1905–1911. doi: 10.1523/JNEUROSCI.06-07-01905.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Novelli A., Nicoletti F., Wroblewski J. T., Alho H., Costa E., Guidotti A. Excitatory amino acid receptors coupled with guanylate cyclase in primary cultures of cerebellar granule cells. J Neurosci. 1987 Jan;7(1):40–47. doi: 10.1523/JNEUROSCI.07-01-00040.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Reymann K. G., Davies S. N., Matthies H., Kase H., Collingridge G. L. Activation of a K-252b-Sensitive Protein Kinase is Necessary for a Post-Synaptic Phase of Long-Term Potentiation in Area CA1 of Rat Hippocampus. Eur J Neurosci. 1990;2(6):481–486. doi: 10.1111/j.1460-9568.1990.tb00439.x. [DOI] [PubMed] [Google Scholar]
  36. Reymann K. G., Matthies H. 2-Amino-4-phosphonobutyrate selectively eliminates late phases of long-term potentiation in rat hippocampus. Neurosci Lett. 1989 Mar 27;98(2):166–171. doi: 10.1016/0304-3940(89)90504-1. [DOI] [PubMed] [Google Scholar]
  37. Schoepp D. D., Johnson B. G. Comparison of excitatory amino acid-stimulated phosphoinositide hydrolysis and N-[3H]acetylaspartylglutamate binding in rat brain: selective inhibition of phosphoinositide hydrolysis by 2-amino-3-phosphonopropionate. J Neurochem. 1989 Jul;53(1):273–278. doi: 10.1111/j.1471-4159.1989.tb07324.x. [DOI] [PubMed] [Google Scholar]
  38. Schoepp D. D., Johnson B. G., Monn J. A. Inhibition of cyclic AMP formation by a selective metabotropic glutamate receptor agonist. J Neurochem. 1992 Mar;58(3):1184–1186. doi: 10.1111/j.1471-4159.1992.tb09381.x. [DOI] [PubMed] [Google Scholar]
  39. Shirasaki T., Klee M. R., Nakaye T., Akaike N. Differential blockade of bicuculline and strychnine on GABA- and glycine-induced responses in dissociated rat hippocampal pyramidal cells. Brain Res. 1991 Oct 4;561(1):77–83. doi: 10.1016/0006-8993(91)90751-g. [DOI] [PubMed] [Google Scholar]
  40. Shirasaki T., Munakata M., Akaike N. Heterogeneous distribution and developmental change of metabotropic glutamate receptors in rat hippocampal CA1 pyramidal neurons. Neurosci Lett. 1993 Jul 23;157(2):191–194. doi: 10.1016/0304-3940(93)90734-3. [DOI] [PubMed] [Google Scholar]
  41. Shirasaki T., Nakagawa T., Wakamori M., Tateishi N., Fukuda A., Murase K., Akaike N. Glycine-insensitive desensitization of N-methyl-D-aspartate receptors in acutely isolated mammalian central neurons. Neurosci Lett. 1990 Jan 1;108(1-2):93–98. doi: 10.1016/0304-3940(90)90712-i. [DOI] [PubMed] [Google Scholar]
  42. Sladeczek F., Récasens M., Bockaert J. A new mechanism for glutamate receptor action: phosphoinositide hydrolysis. Trends Neurosci. 1988 Dec;11(12):545–549. doi: 10.1016/0166-2236(88)90183-x. [DOI] [PubMed] [Google Scholar]
  43. Stanton P. K., Chattarji S., Sejnowski T. J. 2-Amino-3-phosphonopropionic acid, an inhibitor of glutamate-stimulated phosphoinositide turnover, blocks induction of homosynaptic long-term depression, but not potentiation, in rat hippocampus. Neurosci Lett. 1991 Jun 10;127(1):61–66. doi: 10.1016/0304-3940(91)90895-z. [DOI] [PubMed] [Google Scholar]
  44. Sugiyama H., Ito I., Hirono C. A new type of glutamate receptor linked to inositol phospholipid metabolism. Nature. 1987 Feb 5;325(6104):531–533. doi: 10.1038/325531a0. [DOI] [PubMed] [Google Scholar]
  45. Tamaoki T., Nomoto H., Takahashi I., Kato Y., Morimoto M., Tomita F. Staurosporine, a potent inhibitor of phospholipid/Ca++dependent protein kinase. Biochem Biophys Res Commun. 1986 Mar 13;135(2):397–402. doi: 10.1016/0006-291x(86)90008-2. [DOI] [PubMed] [Google Scholar]
  46. Tanabe S., Ito I., Sugiyama H. Possible heterogeneity of metabotropic glutamate receptors induced in Xenopus oocytes by rat brain mRNA. Neurosci Res. 1991 Feb;10(1):71–77. doi: 10.1016/0168-0102(91)90021-p. [DOI] [PubMed] [Google Scholar]
  47. Tanabe Y., Masu M., Ishii T., Shigemoto R., Nakanishi S. A family of metabotropic glutamate receptors. Neuron. 1992 Jan;8(1):169–179. doi: 10.1016/0896-6273(92)90118-w. [DOI] [PubMed] [Google Scholar]
  48. Trombley P. Q., Westbrook G. L. L-AP4 inhibits calcium currents and synaptic transmission via a G-protein-coupled glutamate receptor. J Neurosci. 1992 Jun;12(6):2043–2050. doi: 10.1523/JNEUROSCI.12-06-02043.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Wakamori M., Hidaka H., Akaike N. Hyperpolarizing muscarinic responses of freshly dissociated rat hippocampal CA1 neurones. J Physiol. 1993 Apr;463:585–604. doi: 10.1113/jphysiol.1993.sp019612. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Yamamoto C., Yamashita H., Chujo T. Inhibition and excitation induced by glutamic acid on cerebellar interneurons. Jpn J Physiol. 1977;27(2):225–234. doi: 10.2170/jjphysiol.27.225. [DOI] [PubMed] [Google Scholar]
  51. Zheng F., Gallagher J. P. Metabotropic glutamate receptor agonists potentiate a slow afterdepolarization in CNS neurons. Neuroreport. 1992 Jul;3(7):622–624. doi: 10.1097/00001756-199207000-00020. [DOI] [PubMed] [Google Scholar]

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