Rebound burst firing in the reticular thalamus is not essential for pharmacological absence seizures in mice

Title
Rebound burst firing in the reticular thalamus is not essential for pharmacological absence seizures in mice
Authors
이승은이재광Charles Latchoumane이보영오수진MD.Zahangir Alam Saud박청담Ning Sun정은지Chien-Chang Chen최의주이창준신희섭
Issue Date
2014-08
Publisher
Proceedings of the National Academy of Sciences of the United States of America
Citation
VOL 111, NO 32, 11828-11833
Abstract
Intrinsic burst and rhythmic burst discharges (RBDs) are elicited by activation of T-type Ca2+ channels in the thalamic reticular nucleus (TRN). TRN bursts are believed to be critical for generation and maintenance of thalamocortical oscillations, leading to the spikeand- wave discharges (SWDs), which are the hallmarks of absence seizures. We observed that the RBDs were completely abolished, whereas tonic firing was significantly increased, in TRN neurons from mice in which the gene for the T-type Ca2+ channel, CaV3.3, was deleted (CaV3.3−/−). Contrary to expectations, there was an increased susceptibility to drug-induced SWDs both in CaV3.3−/− mice and in mice in which the CaV3.3 gene was silenced predominantly in the TRN. CaV3.3−/− mice also showed enhanced inhibitory synaptic drive onto TC neurons. Finally, a double knockout of both CaV3.3 and CaV3.2, which showed complete elimination of burst firing and RBDs in TRN neurons, also displayed enhanced drug-induced SWDs and absence seizures. On the other hand, tonic firing in the TRN was increased in these mice, suggesting that increased tonic firing in the TRN may be sufficient for druginduced SWD generation in the absence of burst firing. These results call into question the role of burst firing in TRN neurons in the genesis of SWDs, calling for a rethinking of the mechanism for absence seizure induction.
URI
https://pubs.kist.re.kr/handle/201004/48094
ISSN
00278424
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