Regulation of Hippocampal Gamma Oscillations by Modulation of Intrinsic Neuronal Excitability

Frontiers in Neural Circuits

Neuroscience

Ecem Tütüncü¹  Florian Wildner¹  Alexander Klemz¹  Zoltan Gerevich² 

[1] Institute of Neurophysiology, Charité—Universitätsmedizin, Berlin, Germany;null;

关键词: SK channel;    BK channel;    IK channel;    KCNQ2;    KCNQ3;    Cav3;    Cav3.2;    Cav3.3;   

DOI  :  10.3389/fncir.2021.778022

 received in 2021-09-16, accepted in 2021-12-21,  发布年份 2022

来源: Frontiers

【 摘 要 】

Ion channels activated around the subthreshold membrane potential determine the likelihood of neuronal firing in response to synaptic inputs, a process described as intrinsic neuronal excitability. Long-term plasticity of chemical synaptic transmission is traditionally considered the main cellular mechanism of information storage in the brain; however, voltage- and calcium-activated channels modulating the inputs or outputs of neurons are also subjects of plastic changes and play a major role in learning and memory formation. Gamma oscillations are associated with numerous higher cognitive functions such as learning and memory, but our knowledge of their dependence on intrinsic plasticity is by far limited. Here we investigated the roles of potassium and calcium channels activated at near subthreshold membrane potentials in cholinergically induced persistent gamma oscillations measured in the CA3 area of rat hippocampal slices. Among potassium channels, which are responsible for the afterhyperpolarization in CA3 pyramidal cells, we found that blockers of SK (KCa2) and KV7.2/7.3 (KCNQ2/3), but not the BK (KCa1.1) and IK (KCa3.1) channels, increased the power of gamma oscillations. On the contrary, activators of these channels had an attenuating effect without affecting the frequency. Pharmacological blockade of the low voltage-activated T-type calcium channels (CaV3.1–3.3) reduced gamma power and increased the oscillation peak frequency. Enhancement of these channels also inhibited the peak power without altering the frequency of the oscillations. The presented data suggest that voltage- and calcium-activated ion channels involved in intrinsic excitability strongly regulate the power of hippocampal gamma oscillations. Targeting these channels could represent a valuable pharmacological strategy against cognitive impairment.

【 授权许可】

Unknown   
Copyright © 2022 Klemz, Wildner, Tütüncü and Gerevich.