A Large Lateral Craniotomy Procedure for Mesoscale Wide-field Optical Imaging of Brain Activity

Summary

This protocol presents a method for creating a large unilateral craniotomy over the temporal and parietal regions of the mouse cerebral cortex. This is especially useful for real time imaging over an expansive area of a cortical hemisphere.

Abstract

The craniotomy is a commonly performed procedure to expose the brain for in vivo experiments. In mouse research, most labs utilize a small craniotomy, typically 3 mm x 3 mm. This protocol introduces a method for creating a substantially larger 7 mm x 6 mm cranial window exposing most of a cerebral hemisphere over the mouse temporal and parietal cortices (e.g., bregma 2.5 - 4.5 mm, lateral 0 - 6 mm). To perform this surgery, the head must be tilted approximately 30° and much of the temporal muscle must be retracted. Due to the large amount of bone removal, this procedure is intended only for acute experiments with the animal anesthetized throughout the surgery and experiment.

The main advantage of this innovative large lateral cranial window is to provide simultaneous access to both medial and lateral areas of the cortex. This large unilateral cranial window can be used to study the neural dynamics between cells, as well as between different cortical areas by combining multi-electrode electrophysiological recordings, imaging of neuronal activity (e.g., intrinsic or extrinsic imaging), and optogenetic stimulation. Additionally, this large craniotomy also exposes a large area of cortical blood vessels, allowing for direct manipulation of the lateral cortical vasculature.

Introduction

The craniotomy is a standard procedure used by neuroscientists to reveal a portion of the brain. Since the dawn of electrophysiology, the craniotomy has allowed unprecedented breakthroughs in the field of neuroscience. Dense mapping of the cerebral cortex with electrodes has led to experiments testing hypotheses and theories based on these maps. We have recently entered a new era where the craniotomy is being utilized for in vivo imaging of cortical blood flow^1,2,3 and neurovascular architecture⁴, enabling real time visualization of cortical activity within the exposed areas^5,6,7. Although many studies use craniotomies combined with in vivo optical imaging techniques to study the structure and function of cortical neurons, glia, and cortical vasculature^8,9, further investigations are limited by small areas of exposed cortex (but see¹⁰).

The purpose of this protocol is to provide a method for creating a large lateral craniotomy, exposing the cerebral cortex from the midline to the squamosal bone, and extending beyond bregma and lambda. This large craniotomy enables simultaneous viewing of the association cortices (retrosplenial, cingulate, and parietal), primary and secondary motor, somatosensory, visual, and the auditory cortex. This method has been previously coupled with voltage sensitive dye imaging (VSDI) to investigate how multiple cortical areas interact with one another during spontaneous and stimulus-induced cortical activity^5,11,12. The most challenging aspects of this procedure include positioning the head of the animal, fixing the head plate, and avoiding hemorrhage while separating the temporal muscle from the parietal bone. Care must also be taken during the drilling and skull removal processes as the skull curves at an oblique angle.

Protocol

The following protocol follows the University of Lethbridge Animal Care Committee (ACC) guidelines, and is conducted in accordance with the standards of the Canadian Council on Animal Care (CCAC).

1. Preparation

1. For prolonged study periods, autoclave all opened surgical supplies and ensure that sterility is maintained throughout the surgery. If multiple surgeries are required, autoclave between surgeries. 
2. Ensure there is plenty of brain buffer on hand (at least 50 mL). The solution is comprised of 134 mM sodium chloride, 5.4 mM potassium, 1 mM magnesium chloride hexahydrate, 1.8 mM calcium chloride dihydrate, and 5 mM HEPES sodium, pH balanced to 7.4 with 5 M hydrogen chloride.
3. Place the mouse in an induction chamber and anesthetize with 3 - 4% isoflurane. Follow with 1.0 - 2.0% isoflurane for maintenance during the surgery. Further reduce to as low as 0.4 – 0.8% during imaging^5,13,14,15, provided proper anesthesia is maintained. These low levels of anesthesia require vigilant and frequent monitoring of the mouse (about every 5 min) to ensure it remains areflexic to painful stimuli.
   NOTE: Dehydration can become problematic due to the high surface to volume ratio of the mouse and exacerbated by prolonged use of isoflurane.
   1. Use subcutaneous injections of saline, 0.1 mL per 10 g body weight, every 1 - 2 h. When adequately hydrated, the mouse will urinate once every 1 - 2 h.
4. Closely monitor the mouse to ensure consistent anesthesia throughout surgery and imaging. Do not leave the mouse unattended and take care that it never regains consciousness.
5. Transfer the anesthetized mouse to the head-holder set-up and place on a thermo-regulating heating pad set to 37 °C. Secure the upper teeth in a teeth holder.
6. Rotate the mouse's head towards the left approximately 30° to expose the right lateral side of the head and secure the mouse's head with the blunt end of ear bars (Figure 1A).
7. Apply ophthalmic ointment to prevent corneal drying.
8. To reduce cerebral edema, inject dexamethasone (4 mg/kg) intramuscularly.
9. Wipe the skin over the surgical area with cotton swabs dipped in 4% chlorhexidine (3 times) and 70% ethanol (3 times). Use each cotton swab only once.
10. Don surgical gloves and cover the animal with adhesive plastic wrap. Provide local anesthetic by injecting of lidocaine (8 - 10 mg/kg; 2% epinephrine) subcutaneously over the craniotomy site. Wait 3 - 5 min for the drug to be absorbed into the tissue.

2. Removing the Skin and Retracting the Muscle from the Skull

1. Perform nearly all of these procedures while viewing the skull under a dissecting microscope (e.g., 0.7 - 4.5X power, depending on the situation).
2. Lift up the skin 1 mm left of the midline (just behind the ear) with forceps and make a small horizontal incision with surgical scissors.
3. Make a 5 - 6 mm lateral cut towards the right ear, and then cut towards the rostral end of the head.
4. At the initial incision point, insert the scissors and cut 10 mm rostrally.
5. Cut the skin around the right ear and near the right eye to expose the right side of the skull and temporal muscle. Ensure that the widest part of the exposed area is at least 7 mm. Trim the skin further if the surgical area needs to be extended.
6. Fix the skin around the incision by putting a few drops of butyl cyanoacrylate glue between the skull and the skin. Ensure the tissue has been previously dried with cotton tipped applicators or rolled tissues to increase the efficacy of the adhesive.
7. Using a cotton swab, rub the surface of the skull in a circular motion to remove the periosteum from the skull. Ensure that none remains by drying the skull completely.
8. Using spring scissors and forceps, separate the temporal muscle from the skull; cut and retract the muscle laterally until reaching the squamosal bone (Figure 1C). Take extreme care not to damage the superficial temporal vein that runs along the level of the squamosal bone near the eye, otherwise hemorrhaging might occur.
9. Control bleeding with gel foam pre-soaked in brain buffer. For serious hemorrhaging use a heat cauterizer. Drop butyl cyanoacrylate glue onto the bleeding sites following treatment with the heat cauterizer. Ensure the area is dried beforehand by using cotton tipped applicators or rolled tissues to increase the efficacy of the adhesive. 

3. Craniotomy

NOTE: The surgeon must remain diligent during removal of the skull and dura to avoid unnecessary complications. Troubleshooting steps are included should complications arise.

1. Mark the location of bregma either with a fine tip marker or cut a small triangular piece tape and point a corner at bregma (Figure 2A) to orient the underlying brain regions.
2. Prior to affixing the head plate ensure the skull is completely dry. The skull will quickly air dry after application of the gel foam soaked in brain buffer, if more drying is needed, use cotton tip swabs. This step is crucial for head plate fixation (Figure 1B).
   NOTE: If there is periosteum left on the skull, or if the skull is not dry before gluing on the head plate, it will likely detach. If this happens, gently remove the head plate and start over. Bleeding may occur during this process; allow a few minutes for it to clot, and then gently remove. This process is not recommended to be repeated more than twice.
3. Apply ethyl cyanoacrylate glue around the bottom edge of the head plate¹⁶, and glue the head plate over the craniotomy area (Figure 1D & Figure 2A).
4. Fill the opening space between the skull and head plate with dental cement leaving only the craniotomy area exposed. Wait for the dental cement to dry and harden, typically 5 - 10 min (Figure 2B).
   1. Once the cement is set, briefly fill the well with brain buffer and allow to soak for 3 - 5 min. Use a rolled tissue to remove brain buffer before drilling (Figure 2C).
5. Outline the surgical area by lightly scoring the surface of the skull with a dental drill. Use a pneumatic drill (set to maximum of 20 PSI), with a FG ¼ burr, and controlled with a variable speed foot pedal.
6. Gently trace the drill along the original scoring to deepen it, ensuring the drill does not penetrate through the skull into the brain (Figure 2D). Take turns every few minutes between drilling and dabbing the skull surface with moistened rolled tissues. This will reduce heating and drying of the skull from mechanical friction and prolonged exposure.
   NOTE: The skull will quickly air dry after application of the wet gel foam. If more drying is needed, use cotton tip swabs.
   Caution: The skull is uneven in thickness. For example, the parietal-temporal ridge is the thickest area, while skull regions near the midline and squamosal landmarks are relatively thin.
7. During drilling, periodically check for buckling of the skull by gently pressing on it with forceps or the non-moving drill bit. When the bone begins to buckle, stop drilling and immerse the entire window in brain buffer.
   NOTE: If blood rushes out of an area, it may suggest that the dura has been damaged. If this is the case, place a semi-wet gel foam over the area and try to soak up the blood while gently applying pressure to the gel foam with a cotton tip swab.
8. Wait for at least 5 min before skull removal to soften the bone and to reduce the chance of the dura sticking to the bone, making the skull removal process easier.
9. Perform the skull removal process while the skull is submerged in brain buffer.
   NOTE: If a portion of the skull remains stubbornly attached, a #11 scalpel blade can be used to gently score the skull. Take extreme care to not puncture the blade through the skull and into the brain.
10. Beginning from the anterior edge, gently pry the loose skull from the dura using forceps.
    NOTE: If a small amount of bleeding occurs during the skull removal process, remove the buffer with a transfer pipette or syringe, and then replace with new buffer.
11. Once the bone is loose and "floating" on the dura, firmly grip the bone with forceps and lift the bone from the dura. Ensure the bone never penetrates into the brain.
12. To control bleeding, roll the corner of a tissue into a point and remove most of the buffer from the cranial well. Quickly apply gel foam, pre-soaked in buffer, to the bleeding area while adding very light pressure with a cotton tip swab.
    NOTE: The bleeding usually comes from the edge of the bone or the surface of the dura; both cases are normal and bleeding will quickly stop if no major blood vessels are damaged. If bleeding continues, blood may fill the entire window, forming a clot sheet over the imaging area.
    1. To remove the clot sheet, carefully pick up pieces of clotted blood from the imaging area while leaving the blood clot intact around the source of the ruptured blood vessel. Take care to not remove the blood clot from the bleed source as this may cause even more blood loss. Irrigate the surface of the brain with brain buffer to wash away any blood.
    2. Take care to avoid touching the delicate brain tissue or adding foreign material to the brain; repeat until bleeding has stopped, for approximately 2 - 5 min (Figure 2E).
       NOTE: At this point, the craniotomy is ready for preparing the cranial window (see step 5). If needed, remove the dura before implanting the cranial window (see step 4).

4. Dura Removal

NOTE: Dura removal requires extreme care and may take over 15 min.

1. Draw away excess buffer from the craniotomy. While maintaining a moist surface, grab a small piece of dura with forceps and gently tear the dura.
2. Use forceps and spring scissors to gently tear and cut away the dura.
3. Drop more brain buffer on the brain surface to float the dura and help it separate from the brain. Continue until all dura is removed from the cranial window site. When performed correctly the brain will appear to be very clean with distinct blood vessels and no blemishes (compare Figure 2E with 2F).
   Caution: Some areas of the dura are attached to small arterioles on the surface of the brain (e.g., near the midline proximal to the parietal association area), and removal of such can rupture the arteriole. In such cases, it may be better to leave a small piece of dura intact over top of the arteriole. The VSD may not penetrate that small area, but this is preferred to having major bleeding.
4. Fix the brain surface in agarose as soon as possible to minimize movement from pulsation and to prevent further swelling (see step 5).

5. Preparing Cranial Window

1. Spray the cover glass with 70% ethanol and use an air canister to gently dry. Ensure the glass is completely clean with no spots or dust present.
2. Prepare 1.3% agarose by heating 200 mg of agarose powder dissolved in 15 mL of brain buffer. Set the microwave to high and heat for 10 - 15 s at a time, gently stirring in between, until all agar is dissolved.
   Note: Ensure no bubbles or particles are present, as these will interfere with imaging.
3. Place a thermometer in the hot agarose and cool the agarose down to just above solidifying temperature (~ 40 °C).
   NOTE: Running cool water over the outside of the agarose container may speed the cooling process. Gently stir continuously to ensure no bubbles or particulates are present.
4. Immediately before applying the agar, remove the brain buffer from the cranial well. Draw up the agarose with a transfer pipette and drop the agarose directly on the brain. Quickly place the cover slip over the surface and fasten the cover slip with agarose drops on the corners.

6. Euthanasia

NOTE: In our experience, this procedure takes experienced surgeons at least 3 - 4 practice surgeries to attain greater than 90% success rate. Less experienced surgeons may require even more practice. During the craniotomy or durotomy, the brain may sustain damage, such as if the drill punches through the bone into the brain. Some minor damage at the edge of craniotomy may be permissible. However, if the brain does not look "clean" with bright red undamaged blood vessels and white cortex, the experiment may need to be terminated. Examples of poor preparations include those with dead blood vessels, or when the cortex is marked with torn or damaged blood vessels. If any of these signs are present, the experiment will unlikely yield high quality data. Whether the surgery/experiment was successful or not, humanely euthanize the mouse at the completion of the experiment.

1. Deeply anesthetize with at least 3.5% isoflurane. Then, give an intraperitoneal injection of sodium pentobarbital at 300 mg/kg. Ideally, if the needle is inserted into the liver, death will be very rapid (< 1 min).
2. If perfusion is required, verify that the animal is deeply anesthetized before proceeding (see step 1.3).
3. Alternatively, if perfusion is not required, wait for a minimum of 5 min and then verify that the mouse is dead. Confirm the absence of respiration, heartbeat, as well as a lack of pain withdrawal and corneal reflexes. Also, observe for pale blue/white coloring of extremities and darkening of the blood vessels over the cortex.

Results

To study the interactions between cortical areas within a single hemisphere, we used a large craniotomy extending across the sagittal sinus and 5 - 6 mm lateral. This cranial window included primary (motor, somatosensory, visual, auditory), secondary (motor, visual), and association (retrosplenial, cingulate, parietal association) cortices of right brain hemispheres (Figure 3A). For this work we used voltage sensitive dye (VSD) imaging, which reflects changes...

Discussion

This innovative protocol for a large cranial window enables simultaneous imaging over the temporal and parietal areas of the cerebral cortex. Combined with optical imaging, it can help to reveal neural dynamics within cortical areas during spontaneous and stimulus-induced activity. This expansive craniotomy also exposes a large extension of the cortical vasculature network, including the proximal end of the middle cerebral artery (MCA), enabling in vivo imaging of blood flow and direct manipulation of lateral ve...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Heating Pad	FHC	40-90-2
Fine Scissors	Fine Science Tools	14058-09
Forceps	Fine Science Tools	11251-35	2 or more pairs are recommended
Spring scissors	Fine Science Tools	15000-00, 15000-10	1 pair should be designated for dura removal
Jet tooth shade powder	LANG Dental	Jet Tooth Shade Powder	to be mixed with the Jet Liquid
Jet tooth shade liquid	LANG Dental	Jet Tooth Shade Liquid	to be mixed wihth the Jet Powder
Drill Heads - Carbide Burs FG 1/4 389	Midwest Dental	385201
Agarose Powder	Sigma-Aldrich	A9793
Gelfoam	Sinclair Dental Canada	Pfizer Gelfoam
Isoflurane	Western Drug Distribution Centre Ltd	124125
Lidocaine 2% Epinephrine	Western Drug Distribution Centre Ltd	125299
Dexamethazone 5 mg/mL	Western Drug Distribution Centre Ltd	125231
Butyl cyanoacrylate glue (VetBond)	Western Drug Distribution Centre Ltd	12612