JN Journal of Applied Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 61: 32-44, 1989;
0022-3077/89 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Walsh, J. P.
Right arrow Articles by Byrne, J. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Walsh, J. P.
Right arrow Articles by Byrne, J. H.

Journal of Neurophysiology, Vol 61, Issue 1 32-44, Copyright © 1989 by APS


ARTICLES

Modulation of a steady-state Ca2+-activated, K+ current in tail sensory neurons of Aplysia: role of serotonin and cAMP

J. P. Walsh and J. H. Byrne
Department of Neurobiology and Anatomy, University of Texas Medical School, Houston 77225.

1. The modulation of membrane currents by serotonin (5-HT) was studied in isolated clusters of tail sensory neurons. Serotonin was applied by micropressure ejection onto the somata of sensory neurons voltage-clamped at fixed holding potentials. The range of holding potentials tested in this study was selected to produce a steady-state Ca2+-activated K+ current (IK,Ca). Serotonin induced an inward shift in the holding current associated with a decrease in slope conductance. 2. Intracellular injection of adenosine 3',5'-cyclic monophosphate (cAMP) mimicked the response to 5-HT and induced an inward current associated with a decrease in slope conductance. The responses to 5-HT and cAMP had similar voltage dependencies and both responses were due to an apparent decrease in K+ current. Responses to cAMP were markedly reduced when generated at the peak of a response to 5-HT. The nonsummation of the maximal current responses indicated that 5-HT and cAMP utilize a common, saturable mechanism. 3. In contrast to the consistent decrease in steady-state K+ conductance elicited by cAMP, injection of guanosine 3',5'-cyclic monophosphate (cGMP) produced variable responses. In most cells, cGMP induced outward shifts in holding current that were associated with an increase in slope conductance. 4. Several lines of evidence indicated that IK,Ca contributed to the holding current at the level of membrane potentials that were examined. Inward shifts in holding current associated with a decrease in slope conductance were produced in the presence of agents that block Ca2+ channels, such as Co2+, Cd2+ or Ni2+ and by replacement of extracellular Ca2+ with Ba2+. Reducing the concentration of cytoplasmic Ca2+ through intracellular injection of EGTA had similar effects. Furthermore, inward shifts in holding current were produced by 5 mM tetraethylammonium chloride (TEA), which is known to block IK,Ca in neurons of Aplysia. This concentration of TEA also attenuated the outward current produced in response to direct intracellular injection of Ca2+. 5. Serotonin appears to modulate the IK,Ca that contributes to the steady-state holding current. The same manipulations that block the steady-state IK,Ca (see above) also attenuated the response to 5-HT. Furthermore, K+ currents activated by intracellular injection of Ca2+ were attenuated by 5-HT. 6. These results indicate that the changes in holding current produced by 5-HT are mediated, at least in part, by cAMP. In addition, it appears that 5-HT modulates a steady-state calcium-activated K+ current in addition to the previously described S-current (40, 58) and delayed K+ current (8, 9).(ABSTRACT TRUNCATED AT 250 WORDS)


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
B. Dumitriu, J. E. Cohen, Q. Wan, A. M. Negroiu, and T. W. Abrams
Serotonin Receptor Antagonists Discriminate Between PKA- and PKC-Mediated Plasticity in Aplysia Sensory Neurons
J Neurophysiol, April 1, 2006; 95(4): 2713 - 2720.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. W. Jacklet and D. G. Tieman
Nitric Oxide and Histamine Induce Neuronal Excitability by Blocking Background Currents in Neuron MCC of Aplysia
J Neurophysiol, February 1, 2004; 91(2): 656 - 665.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
J. T. Birmingham and D. L. Tauck
Neuromodulation in invertebrate sensory systems: from biophysics to behavior
J. Exp. Biol., October 15, 2003; 206(20): 3541 - 3546.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
N. Buttner and S. A. Siegelbaum
Antagonistic Modulation of a Hyperpolarization-Activated Cl- Current in Aplysia Sensory Neurons by SCPB and FMRFamide
J Neurophysiol, August 1, 2003; 90(2): 586 - 598.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. R. McDearmid, V. Brezina, and K. R. Weiss
AMRP Peptides Modulate a Novel K+ Current in Pleural Sensory Neurons of Aplysia
J Neurophysiol, July 1, 2002; 88(1): 323 - 332.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. R. Mercer and J. G. Hildebrand
Developmental Changes in the Density of Ionic Currents in Antennal-Lobe Neurons of the Sphinx Moth, Manduca sexta
J Neurophysiol, June 1, 2002; 87(6): 2664 - 2675.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. A. Ungless, X. Gasull, and E. T. Walters
Long-Term Alteration of S-Type Potassium Current and Passive Membrane Properties in Aplysia Sensory Neurons Following Axotomy
J Neurophysiol, May 1, 2002; 87(5): 2408 - 2420.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. L. Purcell and T. J. Carew
Modulation of Excitability in Aplysia Tail Sensory Neurons by Tyrosine Kinases
J Neurophysiol, June 1, 2001; 85(6): 2398 - 2411.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. A. Baxter, C. C. Canavier, J. W. Clark Jr., and J. H. Byrne
Computational Model of the Serotonergic Modulation of Sensory Neurons in Aplysia
J Neurophysiol, December 1, 1999; 82(6): 2914 - 2935.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
P. Kloppenburg, D. Ferns, and A. R. Mercer
Serotonin Enhances Central Olfactory Neuron Responses to Female Sex Pheromone in the Male Sphinx Moth Manduca sexta
J. Neurosci., October 1, 1999; 19(19): 8172 - 8181.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
S. Sugita, D. A. Baxter, and J. H. Byrne
Modulation of a cAMP/Protein Kinase A Cascade by Protein Kinase C in Sensory Neurons of Aplysia
J. Neurosci., October 1, 1997; 17(19): 7237 - 7244.
[Abstract] [Full Text] [PDF]


Home page
Learn. Mem.Home page
G A Clark, R D Hawkins, and E R Kandel
Activity-dependent enhancement of presynaptic facilitation provides a cellular mechanism for the temporal specificity of classical conditioning in Aplysia.
Learn. Mem., January 1, 1994; 1(4): 243 - 257.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online