Comparison of three gamma oscillations in the mouse entorhinal-hippocampal system.
Comparison of three gamma oscillations in the mouse entorhinal-hippocampal system.
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DOI:
10.1111/ejn.13831
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发表时间:
2018-10
期刊:
影响因子:
--
通讯作者:
Paulsen O
中科院分区:
文献类型:
--
作者:
Butler JL;Hay YA;Paulsen O
The entorhinal–hippocampal system is an important circuit in the brain, essential for certain cognitive tasks such as memory and navigation. Different gamma oscillations occur in this circuit, with the medial entorhinal cortex (mEC), CA3 and CA1 all generating gamma oscillations with different properties. These three gamma oscillations converge within CA1, where much work has gone into trying to isolate them from each other. Here, we compared the gamma generators in the mEC, CA3 and CA1 using optogenetically induced theta–gamma oscillations. Expressing channelrhodopsin‐2 in principal neurons in each of the three regions allowed for the induction of gamma oscillations via sinusoidal blue light stimulation at theta frequency. Recording the oscillations in CA1 in vivo, we found that CA3 stimulation induced slower gamma oscillations than CA1 stimulation, matching in vivo reports of spontaneous CA3 and CA1 gamma oscillations. In brain slices ex vivo, optogenetic stimulation of CA3 induced slower gamma oscillations than stimulation of either mEC or CA1, whose gamma oscillations were of similar frequency. All three gamma oscillations had a current sink–source pair between the perisomatic and dendritic layers of the same region. Taking advantage of this model to analyse gamma frequency mechanisms in slice, we showed using pharmacology that all three gamma oscillations were dependent on the same types of synaptic receptor, being abolished by blockade of either type A γ‐aminobutyric acid receptors or α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid/kainate receptors, and insensitive to blockade of N‐methyl‐d‐aspartate receptors. These results indicate that a fast excitatory–inhibitory feedback loop underlies the generation of gamma oscillations in all three regions.
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影响因子:
16.2
作者:
Fries P
通讯作者:
Fries P
影响因子:
3.5
作者:
Mably, Alexandra J.;Gereke, Brian J.;Colgin, Laura Lee
通讯作者:
Colgin, Laura Lee
影响因子:
5.3
作者:
Morita, Kenji;Kalra, Rita;Robinson, Hugh P. C.
通讯作者:
Robinson, Hugh P. C.
DOI:
10.1523/jneurosci.4122-11.2012
发表时间:
2012-01-11
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
Belluscio MA;Mizuseki K;Schmidt R;Kempter R;Buzsáki G
通讯作者:
Buzsáki G
DOI:
10.1111/ejn.13582
发表时间:
2017-06
期刊:
The European journal of neuroscience
影响因子:
--
作者:
Betterton RT;Broad LM;Tsaneva-Atanasova K;Mellor JR
通讯作者:
Mellor JR