GABAergic Excitatory Synapses and Electrical Coupling Sustain Prolonged Discharges in the Prey Capture Neural Network of Clione limacina

• Published in: The Journal of Neuroscience
• Main Author: Norekian, Tigran P.
• Format: Text
• Language: English
• Published: Society for Neuroscience 1999
• Subjects: Article; Clione limacina
• Online Access: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782174/; http://www.ncbi.nlm.nih.gov/pubmed/10024370; https://doi.org/10.1523/JNEUROSCI.19-05-01863.1999

Afterdischarges represent a prominent characteristic of the neural network that controls prey capture reactions in the carnivorous molluscClione limacina. Their main functional implication is transformation of a brief sensory input from a prey into a lasting prey capture response. The present study, which focuses on the neuronal mechanisms of afterdischarges, demonstrates that a single pair of interneurons [cerebral A interneuron (Cr-Aint)] is responsible for afterdischarge generation in the network. Cr-Aint neurons are electrically coupled to all other neurons in the network and produce slow excitatory synaptic inputs to them. This excitatory transmission is found to be GABAergic, which is demonstrated by the use of GABA antagonists, uptake inhibitors, and double-labeling experiments showing that Cr-Aint neurons are GABA-immunoreactive. The Cr-Aint neurons organize three different pathways in the prey capture network, which provide positive feedback necessary for sustaining prolonged spike activity. The first pathway includes electrical coupling and slow chemical transmission from the Cr-Aint neurons to all other neurons in the network. The second feedback is based on excitatory reciprocal connections between contralateral interneurons. Recurrent excitation via the contralateral cell can sustain prolonged interneuron firing, which then drives the activity of all other cells in the network. The third positive feedback is represented by prominent afterdepolarizing potentials after individual spikes in the Cr-Aint neurons. Afterdepolarizations apparently represent recurrent GABAergic excitatory inputs. It is suggested here that these afterdepolarizing potentials are produced by GABAergic excitatory autapses.