4.6 Article

Optical triggered seizures using a caged 4-Aminopyridine

期刊

FRONTIERS IN NEUROSCIENCE
卷 9, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnins.2015.00025

关键词

caged compound; epilepsy model; neocortex; electrophysiology; optical imaging; photostimulation

资金

  1. NINDS [RO1 NS49482]
  2. Clinical and Translational Science Center (CTSC) Grant [UL1 RR 024996]
  3. Cornell University Ithaca-WCMC seed grant
  4. Wellcome Trust [093069]
  5. NEI [DP1EY024503, R01EY011787]
  6. NIHM [R01MH101218, R21MH100646]
  7. NIDA [R21DA034195]
  8. DARPA [W91NF-14-1-0269]
  9. Keck Foundation
  10. U.S. Army Research Laboratory
  11. U.S. Army Research Office [W911NF-12-1-0594]

向作者/读者索取更多资源

Animal models of epilepsy are critical not only for understanding the fundamental mechanism of epilepsy but also for testing the efficacy of new antiepileptic drugs and novel therapeutic interventions. Photorelease of caged molecules is widely used in biological research to control pharmacologic events with high spatio-temporal resolution. We developed a technique for in vivo optical triggering of neocortical seizures using a novel caged compound based on ruthenium photochemistry (RuBi-4AP). Epileptiform events in mouse cortex were induced with blue light in both whole brain and focal illumination. Multi-electrode array recording and optical techniques were used to characterize the propagation of these epileptic events, including interictal spikes, polyspikes, and ictal discharges. These results demonstrate a novel optically-triggered seizure model, with high spatio-temporal control, that could have widespread application in the investigation of ictal onset, propagation and to develop novel light-based therapeutic interventions.

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