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Acta Physiologica 2007; Volume 190, Supplement 656
The Scandinavian Physiological Society's Annual Meeting
8/10/2007-8/12/2007
Oslo, Norway
MECHANISMS AND CHOLINERGIC MODULATION OF SUBTHRESHOLD OSCILLATIONS, THETA RESONANCE, AFTER-HYPERPOLARIZATIONS (AHPS), AND BURSTING IN CA3 HIPPOCAMPAL PYRAMIDAL NEURONS
Abstract number: P16
Sharifullina1 E, Storm1 JF
1Department of Physiology, IBM and Centre of Molecular Biology and Neuroscience, University of Oslo, PB 1103 Blindern, N-0317 Oslo, Norway
Relatively little is known about subthreshold theta resonance and after-hyperpolarization (AHP) mechanisms in CA3 pyramidal neurons processes that may be important for hippocampal theta oscillatons, excitability and plasticity. Using whole cell patch clamp recordings in rat hippocampal slices, after blocking fast synaptic transmission, we found that CA3 pyramidal cells showed subthreshold (beyond 60 mV) membrane potential oscillations (MPOs, n=24) at 49 Hz, and typical M-resonance (Hu & al. 2002). Thus, injection of an oscillating current with increasing frequency (ZAP) evoked MPOs with a resonance peak in the theta range. The spontaneous MPOs and resonance were suppressed by TTX (n=7). The M-channel blocker XE 991 (10 M) partially suppressed the spontaneous MPOs and reduced their frequency, and the M-resonance and medium-duration AHP (mAHP) were blocked (n=7). Carbachol (30 M) produced a similar suppression (n=9), whereas 1 M atropine caused recovery of MPOs, as expected for muscarinic suppression of M-current-dependent processes. In contrast, H-resonance, which is mediated by HCN/h current, was observed at hyperpolarized membrane potentials (70 to 80 mV) and was not blocked by carbachol or TTX, but was suppressed by the h-channel blocker ZD7288 (10 M, n=5). These results indicate that CA3 hippocampal pyramidal cells are equipped with voltage-dependent dual mechanisms of theta resonance: M- and H-resonance, caused by M-, NaP- and h-currents, and in addition M-current-dependent mAHP and spike frequency adaptation mechanisms, similar to those found in CA1 cells. These mechanisms are likely to contribute to hippocampal theta oscillations and excitability control. [Supported by NFR/ SFF/ STORFORSK/ FUGE]
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Acta Physiologica 2007; Volume 190, Supplement 656 :P16