Abstract

Background: Potassium channels have been shown to be involved in neural plasticity and learning. Kv4.2 is a subunit of the A-type potassium channel. Kv4.2 channels modulate excitability in the dendrites of pyramidal neurons in the cortex and hippocampus. Deletion of Kv4.2 results in spatial learning and conditioned fear deficits; however, previous studies have only examined deletion of Kv4.2 in aversive learning tests. Methods: For the current study, we used the Lashley maze as an appetitive learning test. We examined Kv4.2 wildtype (WT) and knockout (KO) mice in the Lashley maze over 4 days during adulthood. The first day consisted of habituating the mice to the maze. The mice then received five trials per day for the next 3 days. The number of errors and the time to the goal box was recorded for each trial. The goal box contained a weigh boat with an appetitive reward (gelatin with sugar). There was an intertrial interval of 15 minutes. Results: We found that Kv4.2 KO mice committed more errors across the trials compared to the WT mice p<0.001. There was no difference in the latency to find the goal box over the period. Discussion: Our finding that deletion of Kv4.2 resulted in more errors in the Lashley maze across 15 trials contribute to a growing body of evidence that Kv4.2 channels are significantly involved in learning and memory.

Highlights

  • Kv4.2 is a subunit of the A–type potassium channel which mediates the excitability of pyramidal neurons in the cortex and hippocampal dendrites1–3

  • Materials and methods Animals: The mice used for this study were Kv4.2 wildtype (WT) and KO adult males that were generated on the 129S6/SvEv background, which had been bred for over 10 generations

  • The Kv4.2 KO mice committed more errors across the 15 trials compared to WT mice

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Summary

Introduction

Kv4.2 is a subunit of the A–type potassium channel which mediates the excitability of pyramidal neurons in the cortex and hippocampal dendrites. When the Kv4.2 subunit is genetically deleted, the A-type current in the CA1 pyramidal cell dendrites of the hippocampus is almost entirely removed. Kv4.2 channels modulate excitability in the dendrites of pyramidal neurons in the cortex and hippocampus. Methods: For the current study, we used the Lashley maze as an appetitive learning test. The number of errors and the time to the goal box was recorded for each trial. Discussion: Our finding that deletion of Kv4.2 resulted in more errors in the Lashley maze across 15 trials contribute to a growing body of evidence that Kv4.2 channels are significantly involved in learning and memory

Methods
Results
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