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Acta Physiologica Congress

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Acta Physiologica 2010; Volume 198, Supplement 677
Joint Meeting of the Scandinavian and German Physiological Societies
3/27/2010-3/30/2010
Copenhagen, Denmark


HIPPOCAMPAL THETA OSCILLATIONS IN CAV2.3 DEFICIENT MICE
Abstract number: O-TUE-2-7

WEIERGRABER1 M, MULLER1 R, STRUCK1 H, KLOSTERKOTTER1 J, HESCHELER1 J, SCHNEIDER1 T

Hippocampal theta oscillations are key elements in various behavioral and cognitive processes. Based on the dualistic theory of theta activity, one can differentiate between atropine-sensitive and atropine-insensitive theta activity. Urethane- induced atropine-sensitive theta oscillations are driven by muscarinic signal transduction pathways with PLCb1 deletion resulting in complete abolishment of theta oscillations. Recent findings illustrate that Cav2.3 Ca2+ channels are important targets of muscarinic signalling in the hippocampus mediating plateau potential generation and epileptiform bursting. In addition, they might be involved in complex rhythm generation and maintenance in the septohippocampal network. To investigate the physiological implications of Cav2.3 Ca2+ channels in hippocampal theta oscillations we performed radiotelemetric deep, intrahippocampal (CA1) recordings in urethane (800 mg/kg ip.) and atropine (50 mg/kg ip.) treated control and Cav2.3-/- mice followed by frequency analysis of EEG data. Our results demonstrate, that Cav2.3 ablation other than PLCb1 deletion does not result in complete abolishment of urethane-induced theta- oscillation and is only partially inhibited by subsequent atropine treatment. In addition, sensory stimuli were also capable of inducing theta activity in Cav2.3-/- mice. Frequency analysis of EEG recordings further suggests that theta oscillation architecture is altered in Cav2.3 deficient mice. Our data suggest for the first time, that Cav2.3 voltage-gated gated Ca2+-channels are an important factor in septohippocampal synchronization associated with theta oscillation.

To cite this abstract, please use the following information:
Acta Physiologica 2010; Volume 198, Supplement 677 :O-TUE-2-7

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