Jun 06, 2024

Public workspacePlug Removal for acute in vivo Electrophysiology Experiments

Plug Removal for acute in vivo Electrophysiology Experiments
  • 1Allen Institute for Neural Dynamics
Open access
Protocol CitationRyan Gillis, Mikayla Carlson, Severine Durand 2024. Plug Removal for acute in vivo Electrophysiology Experiments. protocols.io https://dx.doi.org/10.17504/protocols.io.eq2lywz8qvx9/v1
Manuscript citation:
SHIELD: Skull-shaped hemispheric implants enabling large-scale-electrophysiology datasets in the mouse brain
Bennett, C., Ouellette, B., Ramirez, T. K., et al. bioRxiv 2023.11.12.566771; doi: https://doi.org/10.1101/2023.11.12.566771
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License,  which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: March 20, 2024
Last Modified: June 18, 2024
Protocol Integer ID: 97023
Keywords: electrophysiology, Neuropixels, whole-hemisphere
Abstract
This protocol describes the procedure for removing the SORTA-clear plug used in acute in vivo electrophysiology experiments in whole-hemisphere craniotomy (WHC) preparation mice with Neuropixels probes. This exact methodology is crucial to these experiments due to the role the SORTA-clear plug plays in preserving the brain prior to the described procedure. After the mice undergo a WHC surgery, the implant used to replace the skull on the left hemisphere is covered with a SORTA-clear plug, which keeps the brain from potentially interacting with air or debris, as the SORTA-clear seals the holes in the implant and thus ensures the brain stays healthy between surgery recovery, training, and subsequent experiments. However, we cannot insert Neuropixels probes through SORTA-clear, meaning we must remove it before the experiment. After the SORTA-clear is removed, we place another temporary seal over the brain - Kwik-Cast. This is a more temporary measure and acts as another easily removable seal to preserve the brain just prior to recording. We recommend doing this procedure 1 day prior to the procedure outlined in Neuropixels Data Collection: Whole Hemisphere Recordings as to not expose the mouse to anesthesia on the day of recording, but if necessary, this procedure can be done on the same day as a recording as long as the mouse is given two hours to recover from the anesthesia.
Guidelines
Only perform this procedure in accordance with IACUC and veterinary requirements.
Materials
Anesthesia

ReagentIsofluranePatterson VeterinaryCatalog #07-890-8115

Reagents
MaterialVendorPart #Specifications
ACSF.VIn housen/a10mL


Surgical tools and supplies
MaterialManufacturerPart #
45° forceps*DumontFine Science Tools 11251-35
Glad Press'n Seal*Glad78616
Alcohol Wipes*BD326895
I-DROP 0.25% Viscoadaptive hyaluronan*VET PLUS261
C Universal 4-META Catalyst, 0.7 mLParkellS371
B Quick Base for MetaBond, 10 mL ParkellS398
Radiopaque L-Powder, white, 5gParkellS396
Kwik-Cast SealantWorld Precision InstrumentsKWIK-CAST
Ceramic mixing dish*ParkellS387
Plastic surgical drapeIn houseN/A
*or equivalent


Before start
Please note that this protocol is meant for mice that have previously undergone and recovered from a Whole-Hemisphere Craniotomy surgery.
Graphical overview of procedure
Graphical overview of procedure

plug removal.JPG


Prepare the surgical rig and anesthesia system
Prepare the surgical rig and anesthesia system
Cover heating pad with Press'n Seal and ensure that the heating pad is turned on to Temperature36-37 °C

Obtain a container of ice and place the Metabond tray and a Amount10 mL syringe of ACSF on top of the ice

Ensure the vacuum gauge is set to 10-10 pounds per square inch (PSI) and that all vacuum lines are functioning correctly for both the induction chamber and nosecone scoop. 

Connect induction chamber to the isoflurane and oxygen (if not already connected). 
Ensure the oxygen regulator is set to 0.8-1 L/min.  
Double check all the gas tubing to ensure the system is connected correctly.  
Anesthetize the mouse
Anesthetize the mouse
Open the vacuum valve and isoflurane valves. Direct the flow to the induction chamber. 
Remove the animal from its experimental cage and place the mouse into the induction chamber
Turn the isoflurane regulator to setting Concentration5 % (v/v)
Once the mouse is fully unconscious, turn off the isoflurane. Leave the oxygen and vacuum lines open.  
Transfer and position the mouse on the heating pad and attach the headpost into the clamp. 
Secure the nose cone over the mouse’s snout. Make sure the body of the mouse is on top of the thermometer on heating pad. 
Redirect isoflurane flow from the induction chamber to the surgical rig. 
Turn the isoflurane regulator to Concentration1-2 % (v/v)

Turn off the vacuum line of the induction chamber and close the lid. 
Continue to monitor the mouse’s breathing throughout the procedure
Note
If the breathing is rapid and shallow, increase the isoflurane level as needed in ~.25% increments. If the breathing is too deep, decrease the isoflurane level as needed in ~.25% increments.  

Cover the mouse’s eyes with a drop of I-DROP on each eye to keep them moist. 
Note
These mice are used for experiments involving visual stimuli, so their vision needs to be unobstructed by the time of recording. Any eye lubricant is appropriate if you do not have these experimental constraints.

Place plastic surgical drape over mouse and screw the drape into place with an Allen key 

image (4)(1).png



Paint the inside of the well with white Metabond to facilitate probe visibility during insertion
Paint the inside of the well with white Metabond to facilitate probe visibility during insertion
Remove the plastic snap-on cap from the well 
Gently swab the inside of the well three times with ethanol wipes to remove debris and dust 
While the ethanol evaporates, prepare the white Metabond 
Mix 4 drops of Quick Base for MetaBond, 1 drop of Universal 4-META Catalyst, and 2 even scoops of Radiopaque L-Powder Metabond in the ceramic plate




Stir well with a toothpick 
Apply a thin layer of Metabond in a ring around the edge of the implant with a toothpick. The working time of Metabond ranges from 2-3 minutes from the time the powder is mixed with the base and catalyst to the time it begins setting, so it is important to work quickly during this step. The Metabond will thicken during the working time but should remain a liquid.
Note
Take care not to get any Metabond on the SORTA-clear plug


Wait for the Metabond to dry completely. Use a toothpick to poke the Metabond - advance if it feels hard to the touch
Note
Metabond drying time is variable and depends largely on both the mixture quality and temperature. The best way to see if it is dry is feel it harden with a toothpick.


Remove the SORTA-clear plug
Remove the SORTA-clear plug
Ensure the well is clear of excess debris 
Note
Rinse the well with ACSF if necessary 

Fill the well with enough ACSF to cover the plug, around 3-4 drops.
With forceps, find the anterior or posterior edge of the SORTA-clear plug  
Note
You can poke the edge of the SORTA-clear plug to find the location where you can best grip the SORTA-clear with the forceps (this can vary from mouse to mouse).

Gently peel the SORTA-clear plug off the implant, generally from the posterior or anterior edge.
Once the plug has completely separated, comb the edge of each hole in the implant with small forceps to ensure that the SORTA-clear plug successfully and cleanly detached from the implant 
After SORTA-Clear plug has been removed
After SORTA-Clear plug has been removed
When all implant holes are clear of any debris or SORTA-clear, remove the ACSF from the well with 1-2 Sugi spears 
Fill the well with Kwik-Cast  
Note
Be careful not to submerge the ground wire too deep in Kwik-Cast as it may detach if pulled too harshly

Wait for the Kwik-Cast to dry, then replace the snap-on cap on the well  
Surgery takedown
Surgery takedown
Unscrew the plastic hand rest  
Turn off the isoflurane and oxygen 
Remove the mouse and recover it in its cage 
Clean surgery station with 70% ethanol