DEVELOPMENT AND EPILEPTOGENIC AGENTS MODULATE AN IDENTIFIED ELECTRICAL SYNAPSE

Author(s):  
S.G. Rayport
Keyword(s):  
2009 ◽  
Vol 101 (5) ◽  
pp. 2339-2347 ◽  
Author(s):  
Margaret Lin Veruki ◽  
Espen Hartveit

Gap junction channels constitute specialized intercellular contacts that can serve as electrical synapses. In the rod pathway of the retina, electrical synapses between AII amacrine cells express connexin 36 (Cx36) and electrical synapses between AII amacrines and on-cone bipolar cells express Cx36 on the amacrine side and Cx36 or Cx45 on the bipolar side. For physiological investigations of the properties and functions of these electrical synapses, it is highly desirable to have access to potent pharmacological blockers with selective and reversible action. Here we use dual whole cell voltage-clamp recordings of pairs of AII amacrine cells and pairs of AII amacrine and on-cone bipolar cells in rat retinal slices to directly measure the junctional conductance ( Gj) between electrically coupled cells and to study the effect of the drug meclofenamic acid (MFA) on Gj. Consistent with previous tracer coupling studies, we found that MFA reversibly blocked the electrical synapse currents in a concentration-dependent manner, with complete block at 100 μM. Whereas MFA evoked a detectable decrease in Gj within minutes of application, the time to complete block of Gj was considerably longer, typically 20–40 min. After washout, Gj recovered to 20–90% of the control level, but the time to maximum recovery was typically >1 h. These results suggest that MFA can be a useful drug to investigate the physiological functions of electrical synapses in the rod pathway, but that the slow kinetics of block and reversal might compromise interpretation of the results and that explicit monitoring of Gj is desirable.


1986 ◽  
Vol 125 (1) ◽  
pp. 245-269 ◽  
Author(s):  
W. J. Heitler ◽  
K. Fraser

The anatomy and physiology of the segmental giant (SG) neurone of the fourth abdominal ganglion of the hermit crab is described. The SG has an apparently blindending axon in the first root and a small cell body in the anterior ipsilateral ventral quadrant of the ganglion. There is a large ipsilateral neuropile arborization with prominent dendrites lined up along the course of the ipsilateral giant fibre (GF). The SG receives 1:1 input from the ipsilateral GF via an electrical synapse which is usually rectifying. SG activation produces a large EPSP in all ipsilateral and some contralateral fast flexor excitor (FF) motor neurones. The major input to FFs resulting from GF activation appears to be mediated via the SG. It also produces a small EPSP in ipsilateral and contralateral motor giant neurones. The properties of the hermit crab SG are compared to those of the crayfish SG, and the implications of the SG for the possible evolutionary paths of the giant fibre system are discussed.


2021 ◽  
Author(s):  
Wolfgang Stein ◽  
Margaret DeMaegd ◽  
Lena Yolanda Braun ◽  
Andrés G Vidal-Gadea ◽  
Allison L Harris ◽  
...  

Like their chemical counterparts, electrical synapses show complex dynamics such as rectification and voltage dependence that interact with other electrical processes in neurons. The consequences arising from these interactions for the electrical behavior of the synapse, and the dynamics they create, remain largely unexplored. Using a voltage-dependent electrical synapse between a descending modulatory projection neuron (MCN1) and a motor neuron (LG) in the crustacean stomatogastric ganglion, we find that the influence of the hyperpolarization-activated inward current (Ih) is critical to the function of the electrical synapse. When we blocked Ih with CsCl, the voltage dependence of the electrical synapse shifted by 18.7 mV to more hyperpolarized voltages, placing the dynamic range of the electrical synapse outside of the range of voltages used by the LG motor neuron (-60.2 mV to -44.9 mV). With dual electrode current- and voltage-clamp recordings, we demonstrate that this voltage shift is due to a sustained effect of Ih on the presynaptic MCN1 axon terminal membrane potential. Ih-induced depolarization of the axon terminal membrane potential increased the electrical postsynaptic potentials and currents. With Ih present, the axon terminal resting membrane potential depolarized, shifting the dynamic range of the electrical synapse towards the functional range of the motor neuron. We thus demonstrate that the function of an electrical synapse is critically influenced by a voltage-dependent ionic current (Ih).


2014 ◽  
Vol 29 ◽  
pp. 64-72 ◽  
Author(s):  
John O’Brien
Keyword(s):  

Author(s):  
Kaijun Wu ◽  
Tao Li ◽  
Mingjun Yan

Based on the study of the synchronization of two electric synapse-coupled Sherman neuron systems, this paper analyzes the rich discharge behavior of Sherman neurons through the peak-to-peak interval bifurcation diagram, which determines the parameter values for the study of the electrical synapse coupling Sherman neuron system synchronization. By using the synchronization difference and the correlation coefficient value, this paper analyzes the synchronous transition process of the two electrical synapse-coupled Sherman neuron systems with the change of coupling intensity and studies the bifurcation behavior of neurons in the two electrical synapse-coupled Sherman neuron systems. The experimental results show the transition process of two electrical synapse-coupled Sherman neurons from nonsynchronized, peak-independent cluster synchronization to fully synchronized. In addition, we study the synchronization process of the ring-connected electrical synapse-coupled Sherman neuron system. The experimental results show that the two electrical synapse-coupled Sherman neuron systems show a similar synchronous transition process.


1983 ◽  
Vol 49 (6) ◽  
pp. 1517-1538 ◽  
Author(s):  
M. P. Kovac ◽  
W. J. Davis ◽  
E. M. Matera ◽  
R. P. Croll

Neurons presynaptic to the phasic paracerebral feeding command interneurons (PCP's; Ref. 55) of Pleurobranchaea were located in the isolated central nervous system (CNS) and studied anatomically by lucifer yellow injection and physiologically by current injection and intracellular recording in normal and ion-substituted seawater during quiescence and fictive feeding. The present paper describes excitatory inputs to PCP's, while the accompanying paper (54) reports inhibitory inputs. Monosynaptic excitors (MSEs) are a group of at least three monopolar neurons per hemiganglion. Two have similar dendritic structures and functional effects. Each MSE monosynaptically excites the PCP's and fires action-potential bursts in phase with PCP bursts during fictive feeding. The class I electrotonic neuron (ETI) is a single, identified monopolar neuron per hemiganglion with a sparse dendritic arborization and no descending axon in the cerebrobuccal connective (CBC). The ETI is coupled with PCP's only by means of a non-rectifying electrical synapse. Paradoxically, ETI receives opposite synaptic inputs from PCP's and fires in antiphase with PCP's during fictive feeding. Class II electrotonic neurons (ETII's) are a group of at least two identified multipolar neurons per hemiganglion with indistinguishable dendritic architectures and similar but distinguishable functional effects. Each cell is coupled with PCP's by means of a nonrectifying electrical synapse. One of the ETII's also delivers graded, long-latency poly-synaptic chemical inputs to PCP's. ETII's have descending axons in the CBC, elicit fictive feeding when depolarized, and fire cyclically and in phase with PCP's during fictive feeding. Polysynaptic excitors (PSEs) are a group of at least two identified monopolar neurons per hemiganglion with similar elaborate dendritic fields and functional effects. Each cell excites PCP's by a long-latency, relatively nongraded polysynaptic pathway. PSEs also have descending axons in the ipsilateral CBC, elicit fictive feeding when depolarized, and fire in phase with PCP's during fictive feeding. PSEs and ETII's are here recognized as subclasses of neurons previously identified as paracerebral neurons. They are inhibited by the same neurons that supply recurrent inhibition to PCP's (47), share excitatory inputs with PCP's, and exhibit a similar "command" capacity. This study thus documents redundancy and functional specialization within a command system controlling a relatively complex rhythmic motor behavior.


Synapse ◽  
2005 ◽  
Vol 56 (3) ◽  
pp. 154-165 ◽  
Author(s):  
Joshua P. Neunuebel ◽  
Mark J. Zoran

2007 ◽  
Vol 97 (3) ◽  
pp. 2191-2203 ◽  
Author(s):  
Jianmei Zhang ◽  
Victor Z. Han ◽  
Johannes Meek ◽  
Curtis C. Bell

Primary afferent fibers from the electroreceptors of mormyrid electric fish use a latency code to signal the intensity of electrical current evoked by the fish's own electric organ discharge (EOD). The afferent fibers terminate centrally in the deep and superficial granular layers of the electrosensory lobe with morphologically mixed chemical–electrical synapses. The granular cells in these layers seem to decode afferent latency through an interaction between primary afferent input and a corollary discharge input associated with the EOD motor command. We studied the physiology of deep and superficial granular cells in a slice preparation with whole cell patch recording and electrical stimulation of afferent fibers. Afferent stimulation evoked large all-or-none electrical excitatory postsynaptic potentials (EPSPs) and large all or none GABAergic inhibitory postsynaptic potentials (IPSPs) in both superficial and deep granular cells. The amplitudes of the electrical EPSPs depended on postsynaptic membrane potential, with maximum amplitudes at membrane potentials between −65 and −110 mV. Hyperpolarization beyond this level resulted in either the abrupt disappearance of EPSPs, a step-like reduction to a smaller EPSP, or a graded reduction in EPSP amplitude. Depolarization to membrane potentials lower than that yielding a maximum caused a linear decrease in EPSP amplitude, with EPSP amplitude reaching 0 mV at potentials between −55 and −40 mV. We suggest that the dependence of EPSP size on postsynaptic membrane potential is caused by close linkage of pre- and postsynaptic membrane potentials through a high-conductance gap junction. We also suggest that this dependence may result in functionally important nonlinear interactions between synaptic inputs.


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