Role for electrical synapses in shaping the output of coupled peptidergic neurons from Lymnaea
| Autor: | Guan Z. Zhu, Neil S. Magoski, Christopher C. Beekharry |
|---|---|
| Rok vydání: | 2014 |
| Předmět: |
Periodicity
Patch-Clamp Techniques Action Potentials Lymnaea stagnalis 03 medical and health sciences Bursting 0302 clinical medicine Electrical Synapses medicine Animals Electrical synapse Molecular Biology 030304 developmental biology Lymnaea Meclofenamic Acid Neurons 0303 health sciences biology Quinine General Neuroscience Gap junction Brain Niflumic Acid Hyperpolarization (biology) biology.organism_classification Isoquinolines 3. Good health Ganglia Invertebrate Coupling (electronics) medicine.anatomical_structure Nitrobenzoates Carbenoxolone Glycyrrhetinic Acid Neurology (clinical) Neuroscience 030217 neurology & neurosurgery Developmental Biology Central Nervous System Agents |
| Zdroj: | Brain research. 1603 |
| ISSN: | 1872-6240 |
| Popis: | Electrically coupled neurons communicate through channel assemblies called gap junctions, which mediate the transfer of current from one cell to another. Electrical synapses ensure spike synchronization and reliable transmission, which influences bursting patterns and firing frequency. The present study concerns an electrically coupled two-neuron network in the gastropod mollusc, Lymnaea stagnalis. The neurons, designated Visceral Dorsal 1 (VD1) and Right Parietal Dorsal 2 (RPD2), are peptidergic, innervate aspects of the cardio-respiratory system, and show strong coupling, such that they fire synchronously. Using dual sharp-electrode current-clamp recording and morphological staining in isolated brain preparations, the hypothesis that the electrical synapse is necessary for accurate network output was tested. We found that both cells make extensive projections within and out of the brain, including across the visceral-parietal connective, which links VD1 and RPD2. Cutting this connective uncoupled the neurons and disrupted the firing rate and pattern of RPD2 more than VD1, consistent with VD1 being the master and RPD2 the follower. The electrical synapse was inhibited by select gap junction blockers, with niflumic acid and 5-nitro-2-(3-phenylpropylamino) benzoic acid decreasing the VD1→RPD2 and RPD2→VD1 coupling coefficients, whereas carbenoxolone, α-glycyrrhetinic acid, meclofenamic acid, and quinine were ineffective. There was little-to-no impact on VD1↔RPD2 firing synchrony or frequency when coupling was reduced pharmacologically. However, in the presence of gap junction blockers, suppressing the activity of VD1 by prolonged hyperpolarization revealed a distinct, low-frequency firing pattern in RPD2. This suggests that strong electrical coupling is key to maintaining a synchronous output and proper firing rate. |
| Databáze: | OpenAIRE |
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