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Optogenetical Stimulation in Acute Brain Slices

Optogenetics & Photostimulation

Channelrhodopsin-2 is a cation channel derived from algae that will open with millisecond precision upon illumination with blue light (excitation maximum around 470 nm) and depolarize neuronal membranes. This can be used to selectively activate neurons and neuronal fibers expressing this protein, replacing the need for unspecific extracellular electric stimulation. In a pilot study, we used this channel in combination with the Rapp OptoElectronic UGA-40 system to map inputs to pyramidal cells in the hippocampus.

Figure 1: Panel A shows 23 illumination locations set using the sequence stimulation function of the UGA-40 and an extracellular recording electrode placed in the stratus radiatum. Panel B shows an overlay of extracellular field potentials in response to 5 ms illumination at each point.

Setup:

  • Upright microscope for electrophysiology

Rapp OptoElectronic Components:

  • UGA-40 – point scanning device
  • DL-473 – 473nm diode laser

 

Data provided by:

Dr. Ole Paulsen & Dr. Michael Kohl

The Neuronal Oscillations Group – Department of Physiology at University of Oxford (Oxford, United Kingdom)

https://rapp-opto.com/wp-content/uploads/2018/10/optogenetical-stimulation-in-acute-brain-slices_icon.png 323 354 Anette https://rapp-opto.com/wp-content/uploads/2023/05/rapp-logo-340pxblau-300x79.png Anette2018-10-23 15:43:482019-05-10 11:40:17Optogenetical Stimulation in Acute Brain Slices

Latest Applications

  • FLIRT: fast local infrared thermogenetics for subcellular control of protein function8. June 2021 - 15:31
  • Following Tubulin Dynamics during Spindle Formation using Photoconversion of mEos223. October 2018 - 18:25
  • Optogenetical Stimulation in Acute Brain Slices23. October 2018 - 15:43

Applications Categories

  • Ablation & Microdissection
  • DNA-Damage
  • Temperature Jump & IR-Lego
  • Uncaging & Photolysis
  • Optogenetics & Photostimulation
  • Photobleaching & FRAP
  • Photoconversion &-switching
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