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. 1994 Jan 1;474(1):27–33. doi: 10.1113/jphysiol.1994.sp019999

Reduction of resting K+ current by metabotropic glutamate and muscarinic receptors in rat CA3 cells: mediation by G-proteins.

N C Guérineau 1, B H Gähwiler 1, U Gerber 1
PMCID: PMC1160292  PMID: 8014895

Abstract

1. Effects of 1S,3R-1-aminocyclopentane-1,3-dicarboxylate (1S,3R-ACPD) acting at metabotropic glutamate receptors (mGluRs), and methacholine (MCh), acting at cholinergic muscarinic receptors, were investigated in CA3 neurones in hippocampal slice cultures using the patch-clamp technique. 2. Both 1S,3R-ACPD (10 microM) and MCh (0.5 microM) activated an inward current associated with a decrease in membrane conductance. The current was observed when the slow calcium-dependent after-hyperpolarizing current (IAHP) and the voltage-dependent current (IM) were not activated, reversed close to the reversal potential for K+ (EK) (Erev = -92.8 +/- 10.7 and -89.2 +/- 8.6 mV for 1S,3R-ACPD and MCh, respectively), varied linearly with membrane potential, and thus corresponds to a leak K+ current. 3. The decrease in K+ conductance elicited with 1S,3R-ACPD (50 microM) was substantially reduced (> 70%) with bath application of (RS)-alpha-methyl-4-carboxyphenylglycine (MCPG, 1 mM), a selective mGluR antagonist and was not mimicked by the enantiomer 1R,3S-ACPD (100 microM). 4. The effects of 1S,3R-ACPD and MCh were mediated by activation of G-proteins since no inward current could be elicited in GDP beta S-loaded cells (500 microM). When cells were dialysed with GTP (100 microM) or GTP gamma S (250 microM), however, the amplitude of the current was significantly enhanced. 5. These findings provide evidence that G-proteins couple the activation of mGluRs and muscarinic receptors to a decrease in leak K+ conductance.

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Selected References

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  1. Andrade R., Malenka R. C., Nicoll R. A. A G protein couples serotonin and GABAB receptors to the same channels in hippocampus. Science. 1986 Dec 5;234(4781):1261–1265. doi: 10.1126/science.2430334. [DOI] [PubMed] [Google Scholar]
  2. Bashir Z. I., Bortolotto Z. A., Davies C. H., Berretta N., Irving A. J., Seal A. J., Henley J. M., Jane D. E., Watkins J. C., Collingridge G. L. Induction of LTP in the hippocampus needs synaptic activation of glutamate metabotropic receptors. Nature. 1993 May 27;363(6427):347–350. doi: 10.1038/363347a0. [DOI] [PubMed] [Google Scholar]
  3. Benson D. M., Blitzer R. D., Landau E. M. An analysis of the depolarization produced in guinea-pig hippocampus by cholinergic receptor stimulation. J Physiol. 1988 Oct;404:479–496. doi: 10.1113/jphysiol.1988.sp017301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. 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]
  5. Desai M. A., Smith T. S., Conn P. J. Multiple metabotropic glutamate receptors regulate hippocampal function. Synapse. 1992 Nov;12(3):206–213. doi: 10.1002/syn.890120305. [DOI] [PubMed] [Google Scholar]
  6. Dodd J., Dingledine R., Kelly J. S. The excitatory action of acetylcholine on hippocampal neurones of the guinea pig and rat maintained in vitro. Brain Res. 1981 Feb 23;207(1):109–127. doi: 10.1016/0006-8993(81)90682-x. [DOI] [PubMed] [Google Scholar]
  7. Dutar P., Nicoll R. A. Classification of muscarinic responses in hippocampus in terms of receptor subtypes and second-messenger systems: electrophysiological studies in vitro. J Neurosci. 1988 Nov;8(11):4214–4224. doi: 10.1523/JNEUROSCI.08-11-04214.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Eaton S. A., Jane D. E., Jones P. L., Porter R. H., Pook P. C., Sunter D. C., Udvarhelyi P. M., Roberts P. J., Salt T. E., Watkins J. C. Competitive antagonism at metabotropic glutamate receptors by (S)-4-carboxyphenylglycine and (RS)-alpha-methyl-4-carboxyphenylglycine. Eur J Pharmacol. 1993 Jan 15;244(2):195–197. doi: 10.1016/0922-4106(93)90028-8. [DOI] [PubMed] [Google Scholar]
  9. Eckstein F., Cassel D., Levkovitz H., Lowe M., Selinger Z. Guanosine 5'-O-(2-thiodiphosphate). An inhibitor of adenylate cyclase stimulation by guanine nucleotides and fluoride ions. J Biol Chem. 1979 Oct 10;254(19):9829–9834. [PubMed] [Google Scholar]
  10. Gerber U., Sim J. A., Gähwiler B. H. Reduction of Potassium Conductances Mediated by Metabotropic Glutamate Receptors in Rat CA3 Pyramidal Cells Does Not Require Protein Kinase C or Protein Kinase A. Eur J Neurosci. 1992;4(9):792–797. doi: 10.1111/j.1460-9568.1992.tb00189.x. [DOI] [PubMed] [Google Scholar]
  11. Gilman A. G. G proteins and dual control of adenylate cyclase. Cell. 1984 Mar;36(3):577–579. doi: 10.1016/0092-8674(84)90336-2. [DOI] [PubMed] [Google Scholar]
  12. Gähwiler B. H. Organotypic monolayer cultures of nervous tissue. J Neurosci Methods. 1981 Dec;4(4):329–342. doi: 10.1016/0165-0270(81)90003-0. [DOI] [PubMed] [Google Scholar]
  13. Halliwell J. V., Adams P. R. Voltage-clamp analysis of muscarinic excitation in hippocampal neurons. Brain Res. 1982 Oct 28;250(1):71–92. doi: 10.1016/0006-8993(82)90954-4. [DOI] [PubMed] [Google Scholar]
  14. Irving A. J., Schofield J. G., Watkins J. C., Sunter D. C., Collingridge G. L. 1S,3R-ACPD stimulates and L-AP3 blocks Ca2+ mobilization in rat cerebellar neurons. Eur J Pharmacol. 1990 Sep 21;186(2-3):363–365. doi: 10.1016/0014-2999(90)90462-f. [DOI] [PubMed] [Google Scholar]
  15. Lancaster B., Adams P. R. Calcium-dependent current generating the afterhyperpolarization of hippocampal neurons. J Neurophysiol. 1986 Jun;55(6):1268–1282. doi: 10.1152/jn.1986.55.6.1268. [DOI] [PubMed] [Google Scholar]
  16. Madison D. V., Lancaster B., Nicoll R. A. Voltage clamp analysis of cholinergic action in the hippocampus. J Neurosci. 1987 Mar;7(3):733–741. doi: 10.1523/JNEUROSCI.07-03-00733.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Madison D. V., Nicoll R. A. Actions of noradrenaline recorded intracellularly in rat hippocampal CA1 pyramidal neurones, in vitro. J Physiol. 1986 Mar;372:221–244. doi: 10.1113/jphysiol.1986.sp016006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Manzoni O., Prezeau L., Rassendren F. A., Sladeczek F., Curry K., Bockaert J. Both enantiomers of 1-aminocyclopentyl-1,3-dicarboxylate are full agonists of metabotropic glutamate receptors coupled to phospholipase C. Mol Pharmacol. 1992 Aug;42(2):322–327. [PubMed] [Google Scholar]
  19. McCormick D. A., von Krosigk M. Corticothalamic activation modulates thalamic firing through glutamate "metabotropic" receptors. Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):2774–2778. doi: 10.1073/pnas.89.7.2774. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Nicoll R. A., Malenka R. C., Kauer J. A. Functional comparison of neurotransmitter receptor subtypes in mammalian central nervous system. Physiol Rev. 1990 Apr;70(2):513–565. doi: 10.1152/physrev.1990.70.2.513. [DOI] [PubMed] [Google Scholar]
  21. Palmer E., Monaghan D. T., Cotman C. W. Trans-ACPD, a selective agonist of the phosphoinositide-coupled excitatory amino acid receptor. Eur J Pharmacol. 1989 Aug 3;166(3):585–587. doi: 10.1016/0014-2999(89)90383-x. [DOI] [PubMed] [Google Scholar]
  22. Schoepp D. D., Conn P. J. Metabotropic glutamate receptors in brain function and pathology. Trends Pharmacol Sci. 1993 Jan;14(1):13–20. doi: 10.1016/0165-6147(93)90107-u. [DOI] [PubMed] [Google Scholar]
  23. Simmons M. A., Mather R. J. Selectivity of the effects of guanosine-5'-O-(2-thiodiphosphate) on agonist inhibition of the M-current in amphibian sympathetic neurons. J Neurosci. 1991 Jul;11(7):2130–2134. doi: 10.1523/JNEUROSCI.11-07-02130.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Stratton K. R., Worley P. F., Baraban J. M. Pharmacological characterization of phosphoinositide-linked glutamate receptor excitation of hippocampal neurons. Eur J Pharmacol. 1990 Sep 21;186(2-3):357–361. doi: 10.1016/0014-2999(90)90461-e. [DOI] [PubMed] [Google Scholar]

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