Abstract
1. A study has been made of the modulation of calcium-activated potassium channels in cultured neurones of avian ciliary ganglia by sodium nitroprusside and L-arginine. 2. Sodium nitroprusside (100 microM) reduced the net outward current by 22 +/- 1% at 4.8 ms (mean +/- s.e. mean) and 25 +/- 1% at 350 ms during a test depolarization to +40 mV from a holding potential of -40 mV. The outward current remained reduced for the duration of the recording following a single application of sodium nitroprusside. These effects did not occur if the influx of calcium ions was first blocked with Cd2+ (500 microM). Application of ferrocyanide (100 microM) reduced the net outward current by only 6 +/- 3% at 350 ms during a test depolarization to +40 mV. 3. L-Arginine (270 microM) reduced the net outward current on average by 19 +/- 2% at 4.8 ms and 22 +/- 2% at 350 ms during a test depolarization to +40 mV. The current remained in this reduced state for the duration of the recording following a single application of L-arginine. These effects were reduced to 11 +/- 1% at 4.8 ms and 11 +/- 2% at 350 ms in the presence of N omega-nitro-L-arginine methyl ester (L-NAME, 100 microM). 4. In order to alleviate the dependence of calcium-activated potassium channels (Ik(Ca)) on the inward flux of calcium ions, the patch-clamp pipettes were filled with a solution containing 100 microM CaCl2, and the Ca2+ in the bathing solution was replaced with EGTA.(ABSTRACT TRUNCATED AT 250 WORDS)
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- Bennett M. R., Burnstock G., Holman M. Transmission from intramural inhibitory nerves to the smooth muscle of the guinea-pig taenia coli. J Physiol. 1966 Feb;182(3):541–558. doi: 10.1113/jphysiol.1966.sp007836. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bennett M. R., Ho S. Adenosine modulation of potassium currents in preganglionic nerve terminals of avian ciliary ganglia. Neurosci Lett. 1992 Mar 16;137(1):41–44. doi: 10.1016/0304-3940(92)90293-g. [DOI] [PubMed] [Google Scholar]
- Bennett M. R., Ho S. Probabilistic secretion of quanta from nerve terminals in avian ciliary ganglia modulated by adenosine. J Physiol. 1991;440:513–527. doi: 10.1113/jphysiol.1991.sp018722. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bennett M. R., Kerr R., Khurana G. Adenosine modulation of calcium currents in postganglionic neurones of avian cultured ciliary ganglia. Br J Pharmacol. 1992 May;106(1):25–32. doi: 10.1111/j.1476-5381.1992.tb14287.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bennett M. R., Kerr R., Nichol K. Adenosine modulation of potassium currents in postganglionic neurones of cultured avian ciliary ganglia. Br J Pharmacol. 1991 Oct;104(2):459–465. doi: 10.1111/j.1476-5381.1991.tb12451.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bredt D. S., Snyder S. H. Nitric oxide, a novel neuronal messenger. Neuron. 1992 Jan;8(1):3–11. doi: 10.1016/0896-6273(92)90104-l. [DOI] [PubMed] [Google Scholar]
- Böhme G. A., Bon C., Stutzmann J. M., Doble A., Blanchard J. C. Possible involvement of nitric oxide in long-term potentiation. Eur J Pharmacol. 1991 Jul 9;199(3):379–381. doi: 10.1016/0014-2999(91)90505-k. [DOI] [PubMed] [Google Scholar]
- Clapp L. H., Gurney A. M. Modulation of calcium movements by nitroprusside in isolated vascular smooth muscle cells. Pflugers Arch. 1991 Jun;418(5):462–470. doi: 10.1007/BF00497774. [DOI] [PubMed] [Google Scholar]
- Cornwell T. L., Lincoln T. M. Regulation of intracellular Ca2+ levels in cultured vascular smooth muscle cells. Reduction of Ca2+ by atriopeptin and 8-bromo-cyclic GMP is mediated by cyclic GMP-dependent protein kinase. J Biol Chem. 1989 Jan 15;264(2):1146–1155. [PubMed] [Google Scholar]
- DE LORENZO A. J. The fine structure of synapses in the ciliary ganglion of the chick. J Biophys Biochem Cytol. 1960 Feb;7:31–36. doi: 10.1083/jcb.7.1.31. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dreyer F. Peptide toxins and potassium channels. Rev Physiol Biochem Pharmacol. 1990;115:93–136. [PubMed] [Google Scholar]
- Dryer S. E., Dourado M. M., Wisgirda M. E. Characteristics of multiple Ca(2+)-activated K+ channels in acutely dissociated chick ciliary-ganglion neurones. J Physiol. 1991 Nov;443:601–627. doi: 10.1113/jphysiol.1991.sp018854. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fenwick E. M., Marty A., Neher E. A patch-clamp study of bovine chromaffin cells and of their sensitivity to acetylcholine. J Physiol. 1982 Oct;331:577–597. doi: 10.1113/jphysiol.1982.sp014393. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fletcher G. H., Chiappinelli V. A. An inward rectifier is present in presynaptic nerve terminals in the chick ciliary ganglion. Brain Res. 1992 Mar 13;575(1):103–112. doi: 10.1016/0006-8993(92)90429-d. [DOI] [PubMed] [Google Scholar]
- Fox A. P., Nowycky M. C., Tsien R. W. Kinetic and pharmacological properties distinguishing three types of calcium currents in chick sensory neurones. J Physiol. 1987 Dec;394:149–172. doi: 10.1113/jphysiol.1987.sp016864. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gola M., Ducreux C., Chagneux H. Ca2(+)-activated K+ current involvement in neuronal function revealed by in situ single-channel analysis in Helix neurones. J Physiol. 1990 Jan;420:73–109. doi: 10.1113/jphysiol.1990.sp017902. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
- Kaang B. K., Pfaffinger P. J., Grant S. G., Kandel E. R., Furukawa Y. Overexpression of an Aplysia shaker K+ channel gene modifies the electrical properties and synaptic efficacy of identified Aplysia neurons. Proc Natl Acad Sci U S A. 1992 Feb 1;89(3):1133–1137. doi: 10.1073/pnas.89.3.1133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kawai T., Watanabe M. Blockade of Ca-activated K conductance by apamin in rat sympathetic neurones. Br J Pharmacol. 1986 Jan;87(1):225–232. doi: 10.1111/j.1476-5381.1986.tb10175.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Khurana G., Bennett M. R. Nitric oxide and arachidonic acid modulation of calcium currents in postganglionic neurones of avian cultured ciliary ganglia. Br J Pharmacol. 1993 Jun;109(2):480–485. doi: 10.1111/j.1476-5381.1993.tb13594.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klein M., Camardo J., Kandel E. R. Serotonin modulates a specific potassium current in the sensory neurons that show presynaptic facilitation in Aplysia. Proc Natl Acad Sci U S A. 1982 Sep;79(18):5713–5717. doi: 10.1073/pnas.79.18.5713. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kuba K., Kumamoto E. Long-term potentiations in vertebrate synapses: a variety of cascades with common subprocesses. Prog Neurobiol. 1990;34(3):197–269. doi: 10.1016/0301-0082(90)90012-6. [DOI] [PubMed] [Google Scholar]
- 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]
- Lancaster B., Pennefather P. Potassium currents evoked by brief depolarizations in bull-frog sympathetic ganglion cells. J Physiol. 1987 Jun;387:519–548. doi: 10.1113/jphysiol.1987.sp016587. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Latorre R., Oberhauser A., Labarca P., Alvarez O. Varieties of calcium-activated potassium channels. Annu Rev Physiol. 1989;51:385–399. doi: 10.1146/annurev.ph.51.030189.002125. [DOI] [PubMed] [Google Scholar]
- Magliola L., Jones A. W. Sodium nitroprusside alters Ca2+ flux components and Ca2(+)-dependent fluxes of K+ and Cl- in rat aorta. J Physiol. 1990 Feb;421:411–424. doi: 10.1113/jphysiol.1990.sp017952. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marsh S. J., Brown D. A. Potassium currents contributing to action potential repolarization in dissociated cultured rat superior cervical sympathetic neurones. Neurosci Lett. 1991 Dec 9;133(2):298–302. doi: 10.1016/0304-3940(91)90593-i. [DOI] [PubMed] [Google Scholar]
- Nelson T. J., Collin C., Alkon D. L. Isolation of a G protein that is modified by learning and reduces potassium currents in Hermissenda. Science. 1990 Mar 23;247(4949 Pt 1):1479–1483. doi: 10.1126/science.247.4949.1479. [DOI] [PubMed] [Google Scholar]
- Roberts W. M., Jacobs R. A., Hudspeth A. J. Colocalization of ion channels involved in frequency selectivity and synaptic transmission at presynaptic active zones of hair cells. J Neurosci. 1990 Nov;10(11):3664–3684. doi: 10.1523/JNEUROSCI.10-11-03664.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stanley E. F. Single calcium channels on a cholinergic presynaptic nerve terminal. Neuron. 1991 Oct;7(4):585–591. doi: 10.1016/0896-6273(91)90371-6. [DOI] [PubMed] [Google Scholar]
- Storm J. F. Action potential repolarization and a fast after-hyperpolarization in rat hippocampal pyramidal cells. J Physiol. 1987 Apr;385:733–759. doi: 10.1113/jphysiol.1987.sp016517. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tanaka K., Minota S., Kuba K., Koyano K., Abe T. Differential effects of apamin on Ca2+-dependent K+ currents in bullfrog sympathetic ganglion cells. Neurosci Lett. 1986 Sep 12;69(3):233–238. doi: 10.1016/0304-3940(86)90485-4. [DOI] [PubMed] [Google Scholar]
- White R. E., Schonbrunn A., Armstrong D. L. Somatostatin stimulates Ca(2+)-activated K+ channels through protein dephosphorylation. Nature. 1991 Jun 13;351(6327):570–573. doi: 10.1038/351570a0. [DOI] [PubMed] [Google Scholar]
- Yoshida A., Oda M., Ikemoto Y. Kinetics of the Ca(2+)-activated K+ channel in rat hippocampal neurons. Jpn J Physiol. 1991;41(2):297–315. doi: 10.2170/jjphysiol.41.297. [DOI] [PubMed] [Google Scholar]