JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 63: 303-318, 1990;
0022-3077/90 $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 Bell, C. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bell, C. C.

Journal of Neurophysiology, Vol 63, Issue 2 303-318, Copyright © 1990 by APS


ARTICLES

Mormyromast electroreceptor organs and their afferent fibers in mormyrid fish. II. Intra-axonal recordings show initial stages of central processing

C. C. Bell
Robert S. Dow Neurological Sciences Institute, Good Samaritan Hospital and Medical Center, Portland, Oregon 97210.

1. Physiologically and morphologically identified primary afferent fibers from mormyromast electroreceptor organs were recorded intracellularly. The fiber recordings were made from the nerve root of the posterior lateral line nerve, where the fibers enter the brain, and from the electrosensory lateral line lobe (ELL), near the central terminals of the fibers. 2. The intracellular recordings reveal a variety of potentials, synaptic and nonsynaptic, in addition to the large orthodromic action potentials from the periphery. The goal of the present study was to describe and interpret these various potentials in mormyromast afferent fibers as a first step in understanding the processing of electrosensory information in ELL. 3. Three types of synaptic potentials were recorded inside mormyromast afferent fibers: 1) electric organ corollary discharge (EOCD) excitatory postsynaptic potentials (EPSPs), driven by the motor command that elicits the electric organ discharge (EOD); 2) EPSPs evoked by electrosensory stimulation of electroreceptors in the skin near the electroreceptor from which the recorded fiber originates or by direct stimulation of an electrosensory nerve; and 3) inhibitory postsynaptic potentials (IPSPs) evoked by electrosensory stimulation of more distant electroreceptors. These synaptic potentials can be attributed to synaptic input to postsynaptic cells in ELL that is observed inside the afferent fibers because of electrical synapses between the fibers and the postsynaptic cells. 4. The peripherally evoked EPSPs could frequently be shown to be unitary. The unitary EPSPs were identical to the orthodromic spikes in originating from a single electroreceptor, in threshold, and in latency shift with increasing stimulus intensity. These similarities suggest that the unitary EPSPs are electrotonic EPSPs caused by impulses in other mormyromast afferent fibers that terminate on some of the same postsynaptic cells as the recorded fiber. The peripherally evoked IPSPs had a longer latency than the EPSPs or orthodromic spikes, requiring the presence of an inhibitory interneuron. 5. The peripherally evoked EPSPs, both unitary and nonunitary, show absolute refractory periods of 3-8 ms, followed by relative refractory periods of approximately 8 ms, when tested with two identical stimuli to a nerve. These refractory periods are interpreted as because of refractoriness in the fine preterminal branches of the axonal arbor. 6. A depolarizing afterpotential is commonly associated with the orthodromic spike and probably results from the successful propagation of the spike into the entire terminal arbor. The depolarizing afterpotential has a refractory period that is similar to that of the peripherally evoked EPSPs and that is also interpreted as refractoriness in the fine preterminal branches.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Exp. Biol.Home page
R. Pusch, G. von der Emde, M. Hollmann, J. Bacelo, S. Nobel, K. Grant, and J. Engelmann
Active sensing in a mormyrid fish: electric images and peripheral modifications of the signal carrier give evidence of dual foveation
J. Exp. Biol., March 15, 2008; 211(6): 921 - 934.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
N. B. Sawtell and A. Williams
Transformations of Electrosensory Encoding Associated with an Adaptive Filter
J. Neurosci., February 13, 2008; 28(7): 1598 - 1612.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. Zhang, V. Z. Han, J. Meek, and C. C. Bell
Granular Cells of the Mormyrid Electrosensory Lobe and Postsynaptic Control Over Presynaptic Spike Occurrence and Amplitude Through an Electrical Synapse
J Neurophysiol, March 1, 2007; 97(3): 2191 - 2203.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
N. B. Sawtell, A. Williams, P. D. Roberts, G. von der Emde, and C. C. Bell
Effects of sensing behavior on a latency code.
J. Neurosci., August 9, 2006; 26(32): 8221 - 8234.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. Engelmann, J. Bacelo, E. van den Burg, and K. Grant
Sensory and Motor Effects of Etomidate Anesthesia
J Neurophysiol, February 1, 2006; 95(2): 1231 - 1243.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
N. B. Sawtell, C. Mohr, and C. C. Bell
Recurrent Feedback in the Mormyrid Electrosensory System: Cells of the Preeminential and Lateral Toral Nuclei
J Neurophysiol, April 1, 2005; 93(4): 2090 - 2103.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
L. Gomez, R. Budelli, K. Grant, and A. A. Caputi
Pre-receptor profile of sensory images and primary afferent neuronal representation in the mormyrid electrosensory system
J. Exp. Biol., June 15, 2004; 207(14): 2443 - 2453.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. Mohr, P. D. Roberts, and C. C. Bell
The Mormyromast Region of the Mormyrid Electrosensory Lobe. I. Responses to Corollary Discharge and Electrosensory Stimuli
J Neurophysiol, August 1, 2003; 90(2): 1193 - 1210.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. Mohr, P. D. Roberts, and C. C. Bell
The Mormyromast Region of the Mormyrid Electrosensory Lobe. II. Responses to Input From Central Sources
J Neurophysiol, August 1, 2003; 90(2): 1211 - 1223.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
V. Z. Han, K. Grant, and C. C. Bell
Rapid Activation of GABAergic Interneurons and Possible Calcium Independent GABA Release in the Mormyrid Electrosensory Lobe
J Neurophysiol, March 1, 2000; 83(3): 1592 - 1604.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
J Meek, K Grant, and C Bell
Structural organization of the mormyrid electrosensory lateral line lobe
J. Exp. Biol., January 5, 1999; 202(10): 1291 - 1300.
[Abstract] [PDF]


Home page
J. Neurosci.Home page
M. Kawasaki and Y.-X. Guo
Parallel Projection of Amplitude and Phase Information from the Hindbrain to the Midbrain of the African Electric Fish Gymnarchus niloticus
J. Neurosci., September 15, 1998; 18(18): 7599 - 7611.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
K. Grant, Y. Sugawara, L. Gomez, V. Z. Han, and C. C. Bell
The Mormyrid Electrosensory Lobe In Vitro: Physiology and Pharmacology of Cells and Circuits
J. Neurosci., August 1, 1998; 18(15): 6009 - 6025.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
C. C. Bell, A. Caputi, and K. Grant
Physiology and Plasticity of Morphologically Identified Cells in the Mormyrid Electrosensory Lobe
J. Neurosci., August 15, 1997; 17(16): 6409 - 6423.
[Abstract] [Full Text] [PDF]




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