4.7 Article

Closed-loop stimulation of the medial septum terminates epileptic seizures

期刊

BRAIN
卷 144, 期 3, 页码 885-908

出版社

OXFORD UNIV PRESS
DOI: 10.1093/brain/awaa450

关键词

epilepsy; closed-loop; medial septum; deep brain stimulation; optogenetics

资金

  1. KAKENHI [18KK0236, 19H03550, 19H05224]
  2. Uehara Memorial Fund
  3. Kanae Foundation for the Promotion of Medical Science
  4. Life Science Foundation of Japan
  5. Szeged Scientists Academy under the Ministry of Human Capacities, Hungary [EMMI : 13725-2/2018/INTFIN]
  6. Ministry of Human Capacities, Hungary [UNKP-18-3, 20391-3/2018/FEKUSTRAT]
  7. Momentum program II of the Hungarian Academy of Sciences
  8. National Research, Development and Innovation Office, Hungary [EFOP-3.6.116-2016-00008, KKP133871/KKP20]
  9. EU Horizon 2020 Research and Innovation Program [739593]
  10. Grants-in-Aid for Scientific Research [19H03550, 19H05224, 18KK0236] Funding Source: KAKEN

向作者/读者索取更多资源

The study demonstrates that closed-loop electrical stimulation of the medial septum can effectively terminate intrahippocampal seizures and suppress secondary generalization, emphasizing the importance of internally driven stimulus timing. By precisely activating medial septum GABAergic neurons, successful intervention in pathological oscillations was achieved, providing a new avenue for future clinical translation in other neurological and psychiatric disorders.
Temporal lobe epilepsy with distributed hippocampal seizure foci is often intractable and its secondary generalization might lead to sudden death. Early termination through spatially extensive hippocampal intervention is not feasible directly, because of the large size and irregular shape of the hippocampus. In contrast, the medial septum is a promising target to govern hippocampal oscillations through its divergent connections to both hippocampi. Combining this 'proxy intervention' concept and precisely timed stimulation, we report here that closed-loop medial septum electrical stimulation can quickly terminate intrahippocampal seizures and suppress secondary generalization in a rat kindling model. Precise stimulus timing governed by internal seizure rhythms was essential. Cell type-specific stimulation revealed that the precisely timed activation of medial septum GABAergic neurons underlaid the effects. Our concept of time-targeted proxy stimulation for intervening pathological oscillations can be extrapolated to other neurological and psychiatric disorders, and has potential for clinical translation.

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