Affiliation:
1. Department of Neuroscience, University of Minnesota, Minneapolis, Minnesota;
2. Department of Neurobiology and Behavior, Cornell University, Ithaca, New York; and
3. Departments of Surgery (Neurosurgery) and Anatomy and Neurobiology, Dalhousie University, Halifax, Nova Scotia, Canada
Abstract
In this study, we examined the contribution of a low-threshold calcium current [ICa(T)] to locomotor-related activity in the neonatal mouse. Specifically, the role of ICa(T)was studied during chemically induced, locomotor-like activity in the isolated whole cord and in a genetically distinct population of ventromedial spinal interneurons marked by the homeobox gene Hb9. In isolated whole spinal cords, cycle frequency was decreased in the presence of low-threshold calcium channel blockers, which suggests a role for ICa(T)in the network that produces rhythmic, locomotor-like activity. Additionally, we used Hb9 interneurons as a model to study the cellular responses to application of low-threshold calcium channel blockers. In transverse slice preparations from transgenic Hb9::enhanced green fluorescent protein neonatal mice, N-methyl-d-aspartate-induced membrane potential oscillations in identified Hb9 interneurons also slowed in frequency with application of nickel when fast, spike-mediated, synaptic transmission was blocked with TTX. Voltage-clamp and immunolabeling experiments confirmed expression of ICa(T)and channels, respectively, in Hb9 interneurons located in the ventromedial spinal cord. Taken together, these results provide support that T-type calcium currents play an important role in network-wide rhythm generation during chemically evoked, fictive locomotor activity.
Publisher
American Physiological Society
Subject
Physiology,General Neuroscience
Cited by
20 articles.
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