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Published on: January 10, 2015
Gap junctions between striatal fast-spiking interneurons regulate spiking activity and synchronization as a function
Johannes Hjorth1, Kim T Blackwell, Jeanette Hellgren Kotaleski
1Computational Biology, School of Computer Science and Communication, Royal Institute of Technology, Albanova University Centre, 106 91 Stockholm, Sweden. hjorth@kth.se
Gap junctions in striatal fast-spiking (FS) interneurons reduce overall spiking but enhance sensitivity to synchronized inputs. This suggests FS networks act as detectors for coordinated cortical activity, impacting basal ganglia function.
Area of Science:
- Neuroscience
- Computational Neuroscience
- Cellular Electrophysiology
Background:
- Striatal fast-spiking (FS) interneurons form sparsely connected networks via gap junctions.
- Gap junctions in cortical FS interneurons promote synchronized spiking, influencing target neuron activity.
- Basal ganglia dysfunction is linked to altered neural synchrony, suggesting a role for FS interneuron coupling.
Purpose of the Study:
- To investigate the impact of gap junctions on activity and spike synchronization in striatal FS interneuron networks.
- To model the functional consequences of electrical coupling between FS interneurons in the striatum.
Main Methods:
- Developed a computational network model of striatal FS interneurons.
- Simulated corticostriatal synaptic inputs to the FS interneuron network.
- Varied gap junction conductance to assess effects on spiking and synchronization.
Main Results:
- Increased gap junction conductance moderately enhanced spike synchrony.
- The primary effect of gap junctions was a reduction in the total number of spikes.
- This spike reduction, due to electrical shunting, was less pronounced with coincident inputs.
Conclusions:
- Electrically coupled striatal FS interneurons may function as collective input detectors.
- The network is particularly sensitive to synchronized synaptic inputs from the cortex.
- Gap junctions modulate FS network activity, potentially influencing basal ganglia-related behaviors like motor control and reward learning.
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