AI Article Synopsis

  • T-type Ca channels are believed to influence theta oscillations in the hippocampus, and the study used advanced techniques to investigate the role of Ca3.2 channels in this process.
  • The research found that Ca3.2 mice showed increased power in theta frequencies, particularly during inactive phases of the dark cycle, indicating a significant alteration in theta activity after Ca3.2 channel ablation.
  • Analysis also revealed reductions in specific genes related to synaptic function and GABA receptors, suggesting a link between these transcriptional changes and the observed alterations in theta activity.

Article Abstract

T-type Ca channels are assumed to contribute to hippocampal theta oscillations. We used implantable video-EEG radiotelemetry and qPCR to unravel the role of Ca3.2 Ca channels in hippocampal theta genesis. Frequency analysis of spontaneous long-term recordings in controls and Ca3.2 mice revealed robust increase in relative power in the theta (4-8 Hz) and theta-alpha (4-12 Hz) ranges, which was most prominent during the inactive stages of the dark cycles. Urethane injection experiments also showed enhanced type II theta activity and altered theta architecture following Ca3.2 ablation. Next, gene candidates from hippocampal transcriptome analysis of control and Ca3.2 mice were evaluated using qPCR. Dynein light chain Tctex-Type 1 (Dynlt1b) was significantly reduced in Ca3.2 mice. Furthermore, a significant reduction of GABA A receptor δ subunits and GABA B1 receptor subunits was observed in the septohippocampal GABAergic system. Our results demonstrate that ablation of Ca3.2 significantly alters type II theta activity and theta architecture. Transcriptional changes in synaptic transporter proteins and GABA receptors might be functionally linked to the electrophysiological phenotype.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806756PMC
http://dx.doi.org/10.1038/s41598-020-79763-4DOI Listing

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